id,toxin_id,toxin,target,uniprot,mechanism
1,T3D0001,Arsenic,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
2,T3D0001,Arsenic,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
3,T3D0001,Arsenic,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
4,T3D0001,Arsenic,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5,T3D0001,Arsenic,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
6,T3D0001,Arsenic,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
7,T3D0001,Arsenic,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
8,T3D0001,Arsenic,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
9,T3D0001,Arsenic,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
11,T3D0001,Arsenic,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
14,T3D0001,Arsenic,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
16,T3D0002,Lead,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
17,T3D0002,Lead,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
18,T3D0002,Lead,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
19,T3D0002,Lead,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
20,T3D0002,Lead,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
21,T3D0002,Lead,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
22,T3D0002,Lead,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
23,T3D0002,Lead,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
24,T3D0002,Lead,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes inproper activation, altering proper functioning of cAMP messenger pathways. (R061)"
25,T3D0002,Lead,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which funtions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
26,T3D0002,Lead,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27,T3D0002,Lead,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
28,T3D0002,Lead,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
29,T3D0002,Lead,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
30,T3D0002,Lead,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
31,T3D0002,Lead,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
32,T3D0002,Lead,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
33,T3D0002,Lead,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
34,T3D0002,Lead,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
35,T3D0002,Lead,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
36,T3D0002,Lead,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
37,T3D0002,Lead,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
38,T3D0002,Lead,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
39,T3D0002,Lead,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
40,T3D0002,Lead,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
41,T3D0002,Lead,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
42,T3D0002,Lead,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
43,T3D0002,Lead,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
86,T3D0005,Polychlorinated biphenyls,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
87,T3D0005,Polychlorinated biphenyls,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
88,T3D0005,Polychlorinated biphenyls,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
97,T3D0005,Polychlorinated biphenyls,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
98,T3D0006,Benzene,Hemoglobin subunit alpha,P69905,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
99,T3D0006,Benzene,Hemoglobin subunit beta,P68871,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
100,T3D0006,Benzene,Hemoglobin subunit gamma-1,P69891,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
101,T3D0006,Benzene,Hemoglobin subunit gamma-2,P69892,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
102,T3D0006,Benzene,Hemoglobin subunit delta,P02042,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
103,T3D0006,Benzene,Hemoglobin subunit epsilon,P02100,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
104,T3D0006,Benzene,Hemoglobin subunit theta-1,P09105,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
105,T3D0006,Benzene,Hemoglobin subunit zeta,P02008,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
106,T3D0006,Benzene,Serum albumin,P02768,The binding of metabolites such as benzene oxide to the blood proteins albumin and haemoglobin lead to decreases in haematological cell counts and bone marrow cellularity. (R016)
107,T3D0006,Benzene,Histone H4,P62805,Direct binding of histone leads to protein damage. (R016)
108,T3D0006,Benzene,Histone H3.1,P68431,Direct binding of histone leads to protein damage. (R016)
109,T3D0006,Benzene,Histone H3.1t,Q16695,Direct binding of histone leads to protein damage. (R016)
110,T3D0006,Benzene,Histone H3.3,P84243,Direct binding of histone leads to protein damage. (R016)
111,T3D0006,Benzene,DNA polymerase subunit gamma-1,P54098,Benzene binding of DNA associated proteins leads to mutagenic effects. (R016)
112,T3D0006,Benzene,Ribonucleoside-diphosphate reductase large subunit,P23921,Benzene binding of DNA associated proteins leads to mutagenic effects. (R016)
113,T3D0006,Benzene,Ribonucleoside-diphosphate reductase subunit M2,P31350,Benzene binding of DNA associated proteins leads to mutagenic effects. (R016)
114,T3D0006,Benzene,Tubulin alpha-1B chain,P68363,Direct binding of tubulin leads to protein damage. (R016)
115,T3D0006,Benzene,Tubulin alpha-3C/D chain,Q13748,Direct binding of tubulin leads to protein damage. (R016)
116,T3D0006,Benzene,Tubulin alpha-4A chain,P68366,Direct binding of tubulin leads to protein damage. (R016)
117,T3D0006,Benzene,Tubulin beta chain,P07437,Direct binding of tubulin leads to protein damage. (R016)
118,T3D0006,Benzene,Tubulin beta-2A chain,Q13885,Direct binding of tubulin leads to protein damage. (R016)
119,T3D0006,Benzene,Tubulin beta-2C chain,P68371,Direct binding of tubulin leads to protein damage. (R016)
120,T3D0006,Benzene,Tubulin beta-3 chain,Q13509,Direct binding of tubulin leads to protein damage. (R016)
121,T3D0006,Benzene,Tubulin beta-4 chain,P04350,Direct binding of tubulin leads to protein damage. (R016)
122,T3D0006,Benzene,Tubulin gamma-1 chain,P23258,Direct binding of tubulin leads to protein damage. (R016)
123,T3D0006,Benzene,DNA topoisomerase 2-alpha,P11388,Benzene binding of DNA associated proteins leads to mutagenic effects. (R016)
124,T3D0006,Benzene,DNA topoisomerase 2-beta,Q02880,Benzene binding of DNA associated proteins leads to mutagenic effects. (R016)
125,T3D0007,Cadmium,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
126,T3D0007,Cadmium,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
127,T3D0007,Cadmium,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
128,T3D0007,Cadmium,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
129,T3D0007,Cadmium,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
130,T3D0007,Cadmium,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
131,T3D0007,Cadmium,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
132,T3D0007,Cadmium,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
133,T3D0007,Cadmium,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
134,T3D0007,Cadmium,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
135,T3D0007,Cadmium,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
136,T3D0007,Cadmium,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
137,T3D0007,Cadmium,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
138,T3D0007,Cadmium,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
139,T3D0007,Cadmium,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
140,T3D0007,Cadmium,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
145,T3D0009,Benzo[a]pyrene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
146,T3D0009,Benzo[a]pyrene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
148,T3D0010,Benzo[b]fluoranthene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
149,T3D0010,Benzo[b]fluoranthene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
150,T3D0011,Chloroform,Potassium voltage-gated channel subfamily H member 2,Q12809,"Chloroform has been shown to block HERG potassium channels, causing cardiac arrest. (R070)"
151,T3D0012,"DDT, P,P'-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
152,T3D0012,"DDT, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
153,T3D0012,"DDT, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
154,T3D0012,"DDT, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
155,T3D0012,"DDT, P,P'-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
156,T3D0012,"DDT, P,P'-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
157,T3D0012,"DDT, P,P'-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
158,T3D0012,"DDT, P,P'-",Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
159,T3D0012,"DDT, P,P'-",Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
160,T3D0012,"DDT, P,P'-",Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
161,T3D0012,"DDT, P,P'-",Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
162,T3D0012,"DDT, P,P'-",Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
163,T3D0012,"DDT, P,P'-",Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
164,T3D0012,"DDT, P,P'-",Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
165,T3D0012,"DDT, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
166,T3D0012,"DDT, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
167,T3D0012,"DDT, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
168,T3D0012,"DDT, P,P'-",Calmodulin,P62158,"DDT inhibits the ability of calmodulin, a calcium mediator in nerves, to transport calcium ions that are essential for the release of neurotransmitters. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
169,T3D0012,"DDT, P,P'-",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
170,T3D0012,"DDT, P,P'-",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
171,T3D0012,"DDT, P,P'-",Androgen receptor,P10275,DDT is also believed to adversely affect the reproductive system by mimicking endogenous hormones and binding to the estrogen and adrogen receptors. (R153)
172,T3D0013,Aroclor 1254,ATP-citrate synthase,P53396,"Aroclor 1254 inhibits ATP-citrate synthase, causing a decrease in fatty acid synthesis. (R204)"
174,T3D0013,Aroclor 1254,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
175,T3D0013,Aroclor 1254,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
176,T3D0013,Aroclor 1254,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
185,T3D0013,Aroclor 1254,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
189,T3D0014,Aroclor 1260,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
190,T3D0014,Aroclor 1260,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
191,T3D0014,Aroclor 1260,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
200,T3D0014,Aroclor 1260,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
202,T3D0015,"Dibenzo[a,h]anthracene",Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
203,T3D0015,"Dibenzo[a,h]anthracene",Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
204,T3D0016,Trichloroethylene,"[Pyruvate dehydrogenase [lipoamide]] kinase isozyme 1, mitochondrial",Q15118,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Dichloroacetic acid is known to inhibit pyruvate dehydrogenase kinase. (R160)"
205,T3D0016,Trichloroethylene,"[Pyruvate dehydrogenase [lipoamide]] kinase isozyme 2, mitochondrial",Q15119,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Dichloroacetic acid is known to inhibit pyruvate dehydrogenase kinase. (R160)"
206,T3D0016,Trichloroethylene,Alcohol dehydrogenase 1A,P07327,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Chloral hydrate inhibits alcohol dehydrogenase. (R161)"
207,T3D0016,Trichloroethylene,Alcohol dehydrogenase 1B,P00325,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Chloral hydrate inhibits alcohol dehydrogenase. (R161) "
208,T3D0016,Trichloroethylene,Alcohol dehydrogenase 1C,P00326,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Chloral hydrate inhibits alcohol dehydrogenase. (R161) "
209,T3D0016,Trichloroethylene,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Chloral hydrate inhibits alcohol dehydrogenase. (R161) "
210,T3D0016,Trichloroethylene,Alcohol dehydrogenase class-3,P11766,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Chloral hydrate inhibits alcohol dehydrogenase. (R161) "
211,T3D0016,Trichloroethylene,Alcohol dehydrogenase 4,P08319,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Chloral hydrate inhibits alcohol dehydrogenase. (R161) "
212,T3D0016,Trichloroethylene,Alcohol dehydrogenase 6,P28332,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Chloral hydrate inhibits alcohol dehydrogenase. (R161) "
214,T3D0017,Dieldrin,Alpha-synuclein,P37840,"Dieldrin binds to alpha-synuclein, leading to the formation of intracellular fibrils. (R155)"
215,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
216,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
217,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
218,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
219,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
220,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
221,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
222,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
223,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
224,T3D0017,Dieldrin,Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
225,T3D0017,Dieldrin,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
226,T3D0017,Dieldrin,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
227,T3D0017,Dieldrin,Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
228,T3D0017,Dieldrin,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
229,T3D0017,Dieldrin,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
230,T3D0017,Dieldrin,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
231,T3D0017,Dieldrin,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
232,T3D0017,Dieldrin,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
233,T3D0017,Dieldrin,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
234,T3D0017,Dieldrin,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
235,T3D0017,Dieldrin,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
236,T3D0017,Dieldrin,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
237,T3D0017,Dieldrin,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
238,T3D0017,Dieldrin,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
239,T3D0017,Dieldrin,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
240,T3D0017,Dieldrin,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
241,T3D0017,Dieldrin,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
242,T3D0017,Dieldrin,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
243,T3D0017,Dieldrin,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
244,T3D0017,Dieldrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
245,T3D0017,Dieldrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
246,T3D0017,Dieldrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
247,T3D0018,"Chromium, hexavalent",Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
248,T3D0018,"Chromium, hexavalent",Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
249,T3D0018,"Chromium, hexavalent",Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
250,T3D0018,"Chromium, hexavalent",Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
258,T3D0020,Chlordane,Steroid hormone receptor ERR1,P11474,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162) 
259,T3D0020,Chlordane,Steroid hormone receptor ERR2,O95718,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162) 
260,T3D0020,Chlordane,Estrogen-related receptor gamma,P62508,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162)
261,T3D0020,Chlordane,Retinoic acid receptor beta,P10826,"Chlordane has been shown to bind and activate retinoic acid receptor, causing various developmental defects. (R163)"
262,T3D0020,Chlordane,Retinoic acid receptor gamma-1,P13631,"Chlordane has been shown to bind and activate retinoic acid receptor, causing various developmental defects. (R163)"
264,T3D0021,"DDE, P,P'-",Androgen receptor,P10275,DDE is also believed to adversely affect the reproductive system by mimicking endogenous hormones and binding to the estrogen and adrogen receptors. (R153) 
265,T3D0021,"DDE, P,P'-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
266,T3D0021,"DDE, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
267,T3D0021,"DDE, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
268,T3D0021,"DDE, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
269,T3D0021,"DDE, P,P'-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
270,T3D0021,"DDE, P,P'-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
271,T3D0021,"DDE, P,P'-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
272,T3D0021,"DDE, P,P'-",Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
273,T3D0021,"DDE, P,P'-",Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
274,T3D0021,"DDE, P,P'-",Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
275,T3D0021,"DDE, P,P'-",Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
276,T3D0021,"DDE, P,P'-",Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
277,T3D0021,"DDE, P,P'-",Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
278,T3D0021,"DDE, P,P'-",Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
279,T3D0021,"DDE, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
280,T3D0021,"DDE, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
281,T3D0021,"DDE, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
282,T3D0021,"DDE, P,P'-",Calmodulin,P62158,"DDE inhibits the ability of calmodulin, a calcium mediator in nerves, to transport calcium ions that are essential for the release of neurotransmitters. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
283,T3D0021,"DDE, P,P'-",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
284,T3D0021,"DDE, P,P'-",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
289,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
290,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
291,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
292,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
293,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
294,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
295,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
296,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
297,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
298,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
299,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
300,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
301,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
302,T3D0024,Aldrin,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
303,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
304,T3D0024,Aldrin,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
305,T3D0024,Aldrin,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
306,T3D0024,Aldrin,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
307,T3D0024,Aldrin,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
308,T3D0024,Aldrin,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
309,T3D0024,Aldrin,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
310,T3D0024,Aldrin,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
311,T3D0024,Aldrin,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
312,T3D0024,Aldrin,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
313,T3D0024,Aldrin,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
314,T3D0024,Aldrin,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
315,T3D0024,Aldrin,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
316,T3D0024,Aldrin,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
317,T3D0024,Aldrin,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
318,T3D0024,Aldrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
319,T3D0024,Aldrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
320,T3D0024,Aldrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
322,T3D0025,"DDD, P,P'-",Androgen receptor,P10275,DDD is also believed to adversely affect the reproductive system by mimicking endogenous hormones and binding to the estrogen and adrogen receptors. (R153) 
323,T3D0025,"DDD, P,P'-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
324,T3D0025,"DDD, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
325,T3D0025,"DDD, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
326,T3D0025,"DDD, P,P'-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
327,T3D0025,"DDD, P,P'-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
328,T3D0025,"DDD, P,P'-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
329,T3D0025,"DDD, P,P'-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
330,T3D0025,"DDD, P,P'-",Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
331,T3D0025,"DDD, P,P'-",Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
332,T3D0025,"DDD, P,P'-",Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
333,T3D0025,"DDD, P,P'-",Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
334,T3D0025,"DDD, P,P'-",Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
335,T3D0025,"DDD, P,P'-",Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
336,T3D0025,"DDD, P,P'-",Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
337,T3D0025,"DDD, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
338,T3D0025,"DDD, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
339,T3D0025,"DDD, P,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
340,T3D0025,"DDD, P,P'-",Calmodulin,P62158,"DDD inhibits the ability of calmodulin, a calcium mediator in nerves, to transport calcium ions that are essential for the release of neurotransmitters. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
341,T3D0025,"DDD, P,P'-",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
342,T3D0025,"DDD, P,P'-",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
346,T3D0027,Aroclor 1248,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015) "
347,T3D0027,Aroclor 1248,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203) "
348,T3D0027,Aroclor 1248,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
357,T3D0027,Aroclor 1248,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071) 
358,T3D0028,Cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
359,T3D0028,Cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
360,T3D0028,Cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
361,T3D0028,Cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
362,T3D0028,Cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
363,T3D0028,Cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
364,T3D0028,Cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
365,T3D0028,Cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
366,T3D0028,Cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
367,T3D0028,Cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
368,T3D0028,Cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
369,T3D0028,Cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
370,T3D0028,Cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
371,T3D0028,Cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
372,T3D0028,Cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
373,T3D0028,Cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211) 
376,T3D0028,Cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212) 
377,T3D0028,Cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212) 
378,T3D0028,Cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212) 
379,T3D0028,Cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212) 
380,T3D0028,Cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212) 
381,T3D0028,Cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212) 
382,T3D0028,Cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214) 
386,T3D0029,Aroclor 1242,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015) "
387,T3D0029,Aroclor 1242,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203) "
388,T3D0029,Aroclor 1242,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
397,T3D0029,Aroclor 1242,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
413,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
414,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
415,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
416,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
417,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
418,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
419,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
420,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
421,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
422,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
423,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
424,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
425,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
426,T3D0031,Toxaphene,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
427,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
428,T3D0031,Toxaphene,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
429,T3D0031,Toxaphene,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
430,T3D0031,Toxaphene,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
431,T3D0031,Toxaphene,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
432,T3D0031,Toxaphene,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
433,T3D0031,Toxaphene,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
434,T3D0031,Toxaphene,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
435,T3D0031,Toxaphene,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
436,T3D0031,Toxaphene,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
437,T3D0031,Toxaphene,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
438,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
439,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
440,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
441,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
442,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
443,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
444,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
445,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
446,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
447,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
448,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
449,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
450,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
451,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
452,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
453,T3D0032,"Hexachlorocyclohexane, gamma-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
454,T3D0032,"Hexachlorocyclohexane, gamma-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
455,T3D0032,"Hexachlorocyclohexane, gamma-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
456,T3D0032,"Hexachlorocyclohexane, gamma-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
457,T3D0032,"Hexachlorocyclohexane, gamma-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
458,T3D0032,"Hexachlorocyclohexane, gamma-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
459,T3D0032,"Hexachlorocyclohexane, gamma-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
460,T3D0032,"Hexachlorocyclohexane, gamma-",Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
461,T3D0032,"Hexachlorocyclohexane, gamma-",Estrogen-related receptor gamma,P62508,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting estrogen-related receptor gamma. (R188)
462,T3D0032,"Hexachlorocyclohexane, gamma-",Androgen receptor,P10275,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the androgen receptor. (R188)
463,T3D0032,"Hexachlorocyclohexane, gamma-",Progesterone receptor,P06401,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the progesterone receptor. (R188)
464,T3D0033,Tetrachloroethylene,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
465,T3D0033,Tetrachloroethylene,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
466,T3D0033,Tetrachloroethylene,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
467,T3D0033,Tetrachloroethylene,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
468,T3D0033,Tetrachloroethylene,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
469,T3D0033,Tetrachloroethylene,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
470,T3D0033,Tetrachloroethylene,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
471,T3D0033,Tetrachloroethylene,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
472,T3D0033,Tetrachloroethylene,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
473,T3D0033,Tetrachloroethylene,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
474,T3D0033,Tetrachloroethylene,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
475,T3D0033,Tetrachloroethylene,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
476,T3D0033,Tetrachloroethylene,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
477,T3D0033,Tetrachloroethylene,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
478,T3D0033,Tetrachloroethylene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
479,T3D0033,Tetrachloroethylene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
480,T3D0033,Tetrachloroethylene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
481,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
482,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
483,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
484,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
485,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
486,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
487,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
488,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
489,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
490,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
491,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
492,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
493,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
494,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
495,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
496,T3D0036,"Hexachlorocyclohexane, beta-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
497,T3D0036,"Hexachlorocyclohexane, beta-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
498,T3D0036,"Hexachlorocyclohexane, beta-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
499,T3D0036,"Hexachlorocyclohexane, beta-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
500,T3D0036,"Hexachlorocyclohexane, beta-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
501,T3D0036,"Hexachlorocyclohexane, beta-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
502,T3D0036,"Hexachlorocyclohexane, beta-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
503,T3D0036,"Hexachlorocyclohexane, beta-",Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
504,T3D0036,"Hexachlorocyclohexane, beta-",Estrogen-related receptor gamma,P62508,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting estrogen-related receptor gamma. (R188)
505,T3D0036,"Hexachlorocyclohexane, beta-",Androgen receptor,P10275,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the androgen receptor. (R188)
506,T3D0036,"Hexachlorocyclohexane, beta-",Progesterone receptor,P06401,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the progesterone receptor. (R188)
508,T3D0039,Benzo[a]anthracene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
509,T3D0039,Benzo[a]anthracene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
510,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
511,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
512,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
513,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
514,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
515,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
516,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
517,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
518,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
519,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
520,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
521,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
522,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
523,T3D0041,Endrin,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
524,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
525,T3D0041,Endrin,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
526,T3D0041,Endrin,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
527,T3D0041,Endrin,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
528,T3D0041,Endrin,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
529,T3D0041,Endrin,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
530,T3D0041,Endrin,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
531,T3D0041,Endrin,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
532,T3D0041,Endrin,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
533,T3D0041,Endrin,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
534,T3D0041,Endrin,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
535,T3D0041,Endrin,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
536,T3D0041,Endrin,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
537,T3D0041,Endrin,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
538,T3D0041,Endrin,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
539,T3D0041,Endrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
540,T3D0041,Endrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
541,T3D0041,Endrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
543,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
544,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
545,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
546,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
547,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
548,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
549,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
550,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
551,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
552,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
553,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
554,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
555,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
556,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
557,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
558,T3D0043,"Hexachlorocyclohexane, delta-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
559,T3D0043,"Hexachlorocyclohexane, delta-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
560,T3D0043,"Hexachlorocyclohexane, delta-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
561,T3D0043,"Hexachlorocyclohexane, delta-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
562,T3D0043,"Hexachlorocyclohexane, delta-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
563,T3D0043,"Hexachlorocyclohexane, delta-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
564,T3D0043,"Hexachlorocyclohexane, delta-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
565,T3D0043,"Hexachlorocyclohexane, delta-",Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
566,T3D0043,"Hexachlorocyclohexane, delta-",Estrogen-related receptor gamma,P62508,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting estrogen-related receptor gamma. (R188)
567,T3D0043,"Hexachlorocyclohexane, delta-",Androgen receptor,P10275,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the androgen receptor. (R188)
568,T3D0043,"Hexachlorocyclohexane, delta-",Progesterone receptor,P06401,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the progesterone receptor. (R188)
569,T3D0048,Aroclor 1221,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
570,T3D0048,Aroclor 1221,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
571,T3D0048,Aroclor 1221,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
580,T3D0048,Aroclor 1221,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
581,T3D0049,Cobalt,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
583,T3D0050,"DDT, O,P'-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
584,T3D0050,"DDT, O,P'-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
585,T3D0050,"DDT, O,P'-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
586,T3D0050,"DDT, O,P'-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
587,T3D0050,"DDT, O,P'-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
588,T3D0050,"DDT, O,P'-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
589,T3D0050,"DDT, O,P'-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
590,T3D0050,"DDT, O,P'-",Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
591,T3D0050,"DDT, O,P'-",Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
592,T3D0050,"DDT, O,P'-",Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
593,T3D0050,"DDT, O,P'-",Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
594,T3D0050,"DDT, O,P'-",Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
595,T3D0050,"DDT, O,P'-",Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
596,T3D0050,"DDT, O,P'-",Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
597,T3D0050,"DDT, O,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
598,T3D0050,"DDT, O,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
599,T3D0050,"DDT, O,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
600,T3D0050,"DDT, O,P'-",Calmodulin,P62158,"DDT inhibits the ability of calmodulin, a calcium mediator in nerves, to transport calcium ions that are essential for the release of neurotransmitters. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
601,T3D0050,"DDT, O,P'-",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
602,T3D0050,"DDT, O,P'-",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
603,T3D0050,"DDT, O,P'-",Androgen receptor,P10275,DDT is also believed to adversely affect the reproductive system by mimicking endogenous hormones and binding to the estrogen and adrogen receptors. (R153)
604,T3D0051,Aroclor 1016,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
605,T3D0051,Aroclor 1016,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
606,T3D0051,Aroclor 1016,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
615,T3D0051,Aroclor 1016,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
616,T3D0053,Nickel,Calcineurin subunit B type 1,P63098,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
617,T3D0053,Nickel,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
618,T3D0053,Nickel,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
619,T3D0053,Nickel,Histone H3.1t,Q16695,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
620,T3D0053,Nickel,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
621,T3D0053,Nickel,Protamine-2,P04554,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
625,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
626,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
627,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
628,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
629,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
630,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
631,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
632,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
633,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
634,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit delta,O14764,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
635,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
636,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
637,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit pi,O00591,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
638,T3D0054,Endosulfan,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
639,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
640,T3D0054,Endosulfan,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
641,T3D0054,Endosulfan,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
642,T3D0054,Endosulfan,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
643,T3D0054,Endosulfan,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
644,T3D0054,Endosulfan,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
645,T3D0054,Endosulfan,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
646,T3D0054,Endosulfan,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
647,T3D0054,Endosulfan,Sodium/potassium-transporting ATPase gamma chain,P54710,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
648,T3D0054,Endosulfan,Calcium-transporting ATPase type 2C member 1,P98194,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
649,T3D0054,Endosulfan,Calcium-transporting ATPase type 2C member 2,O75185,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
650,T3D0054,Endosulfan,Plasma membrane calcium-transporting ATPase 1,P20020,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
651,T3D0054,Endosulfan,Plasma membrane calcium-transporting ATPase 2,Q01814,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
652,T3D0054,Endosulfan,Plasma membrane calcium-transporting ATPase 3,Q16720,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
653,T3D0054,Endosulfan,Plasma membrane calcium-transporting ATPase 4,P23634,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
654,T3D0054,Endosulfan,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
655,T3D0054,Endosulfan,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
656,T3D0054,Endosulfan,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
657,T3D0054,Endosulfan,Progesterone receptor,P06401,Endosulfan is an endocrine disruptor and acts as an agonist at the progesterone receptor. (R312)
658,T3D0054,Endosulfan,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
659,T3D0054,Endosulfan,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
660,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
661,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
662,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
663,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
664,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
665,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
666,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
667,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
668,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
669,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit delta,O14764,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
670,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
671,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
672,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit pi,O00591,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
673,T3D0055,Endosulfan sulfate,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
674,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
675,T3D0055,Endosulfan sulfate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
676,T3D0055,Endosulfan sulfate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
677,T3D0055,Endosulfan sulfate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
678,T3D0055,Endosulfan sulfate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
679,T3D0055,Endosulfan sulfate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
680,T3D0055,Endosulfan sulfate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
681,T3D0055,Endosulfan sulfate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
682,T3D0055,Endosulfan sulfate,Sodium/potassium-transporting ATPase gamma chain,P54710,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
683,T3D0055,Endosulfan sulfate,Calcium-transporting ATPase type 2C member 1,P98194,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
684,T3D0055,Endosulfan sulfate,Calcium-transporting ATPase type 2C member 2,O75185,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
685,T3D0055,Endosulfan sulfate,Plasma membrane calcium-transporting ATPase 1,P20020,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
686,T3D0055,Endosulfan sulfate,Plasma membrane calcium-transporting ATPase 2,Q01814,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
687,T3D0055,Endosulfan sulfate,Plasma membrane calcium-transporting ATPase 3,Q16720,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
688,T3D0055,Endosulfan sulfate,Plasma membrane calcium-transporting ATPase 4,P23634,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
689,T3D0055,Endosulfan sulfate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
690,T3D0055,Endosulfan sulfate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
691,T3D0055,Endosulfan sulfate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"Endosulfan sulfate inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
692,T3D0055,Endosulfan sulfate,Progesterone receptor,P06401,Endosulfan sulfate is an endocrine disruptor and acts as an agonist at the progesterone receptor. (R312)
693,T3D0055,Endosulfan sulfate,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
694,T3D0055,Endosulfan sulfate,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
695,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
696,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
697,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
698,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
699,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
700,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
701,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
702,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
703,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
704,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit delta,O14764,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
705,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
706,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
707,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit pi,O00591,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
708,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
709,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit rho-2,P28476,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
710,T3D0057,"Endosulfan, alpha",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
711,T3D0057,"Endosulfan, alpha",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
712,T3D0057,"Endosulfan, alpha",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
713,T3D0057,"Endosulfan, alpha",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
714,T3D0057,"Endosulfan, alpha",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
715,T3D0057,"Endosulfan, alpha",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
716,T3D0057,"Endosulfan, alpha",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
717,T3D0057,"Endosulfan, alpha",Sodium/potassium-transporting ATPase gamma chain,P54710,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
718,T3D0057,"Endosulfan, alpha",Calcium-transporting ATPase type 2C member 1,P98194,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
719,T3D0057,"Endosulfan, alpha",Calcium-transporting ATPase type 2C member 2,O75185,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
720,T3D0057,"Endosulfan, alpha",Plasma membrane calcium-transporting ATPase 1,P20020,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
721,T3D0057,"Endosulfan, alpha",Plasma membrane calcium-transporting ATPase 2,Q01814,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
722,T3D0057,"Endosulfan, alpha",Plasma membrane calcium-transporting ATPase 3,Q16720,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
723,T3D0057,"Endosulfan, alpha",Plasma membrane calcium-transporting ATPase 4,P23634,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
724,T3D0057,"Endosulfan, alpha",Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
725,T3D0057,"Endosulfan, alpha",Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
726,T3D0057,"Endosulfan, alpha",Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
727,T3D0057,"Endosulfan, alpha",Progesterone receptor,P06401,Endosulfan is an endocrine disruptor and acts as an agonist at the progesterone receptor. (R312)
728,T3D0057,"Endosulfan, alpha",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
729,T3D0057,"Endosulfan, alpha",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
730,T3D0060,Dibromochloropropane,NADH-ubiquinone oxidoreductase chain 1,P03886,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
731,T3D0061,Methoxychlor,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
732,T3D0061,Methoxychlor,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
733,T3D0061,Methoxychlor,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
734,T3D0061,Methoxychlor,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
735,T3D0061,Methoxychlor,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
736,T3D0061,Methoxychlor,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
737,T3D0061,Methoxychlor,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
738,T3D0061,Methoxychlor,Sodium/potassium-transporting ATPase gamma chain,P54710,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
739,T3D0061,Methoxychlor,Calcium-transporting ATPase type 2C member 1,P98194,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
740,T3D0061,Methoxychlor,Calcium-transporting ATPase type 2C member 2,O75185,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
741,T3D0061,Methoxychlor,Plasma membrane calcium-transporting ATPase 1,P20020,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
742,T3D0061,Methoxychlor,Plasma membrane calcium-transporting ATPase 2,Q01814,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
743,T3D0061,Methoxychlor,Plasma membrane calcium-transporting ATPase 3,Q16720,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
744,T3D0061,Methoxychlor,Plasma membrane calcium-transporting ATPase 4,P23634,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
745,T3D0061,Methoxychlor,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
746,T3D0061,Methoxychlor,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
747,T3D0061,Methoxychlor,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"Like DDT, methoxychlor may also inhibit neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase and Ca2+-ATPase, which play vital roles in neuronal repolarization. This contributes to the reduced rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029, R325)"
749,T3D0062,Benzo[k]fluoranthene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
750,T3D0062,Benzo[k]fluoranthene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
751,T3D0065,Chromium(VI) oxide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
752,T3D0065,Chromium(VI) oxide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
753,T3D0065,Chromium(VI) oxide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
754,T3D0065,Chromium(VI) oxide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
755,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
756,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
757,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
758,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
759,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
760,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
761,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
762,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
763,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
764,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit delta,O14764,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
765,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
766,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
767,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit pi,O00591,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
768,T3D0067,"Endosulfan, beta",Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
769,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit rho-2,P28476,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
770,T3D0067,"Endosulfan, beta",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
771,T3D0067,"Endosulfan, beta",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
772,T3D0067,"Endosulfan, beta",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
773,T3D0067,"Endosulfan, beta",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
774,T3D0067,"Endosulfan, beta",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
775,T3D0067,"Endosulfan, beta",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
776,T3D0067,"Endosulfan, beta",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
777,T3D0067,"Endosulfan, beta",Sodium/potassium-transporting ATPase gamma chain,P54710,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
778,T3D0067,"Endosulfan, beta",Calcium-transporting ATPase type 2C member 1,P98194,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
779,T3D0067,"Endosulfan, beta",Calcium-transporting ATPase type 2C member 2,O75185,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
780,T3D0067,"Endosulfan, beta",Plasma membrane calcium-transporting ATPase 1,P20020,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
781,T3D0067,"Endosulfan, beta",Plasma membrane calcium-transporting ATPase 2,Q01814,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
782,T3D0067,"Endosulfan, beta",Plasma membrane calcium-transporting ATPase 3,Q16720,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
783,T3D0067,"Endosulfan, beta",Plasma membrane calcium-transporting ATPase 4,P23634,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
784,T3D0067,"Endosulfan, beta",Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
785,T3D0067,"Endosulfan, beta",Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
786,T3D0067,"Endosulfan, beta",Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"Endosulfan inhibits Na+ K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the CNS. This results in hyperexcitation and generalized seizures. (R194)"
787,T3D0067,"Endosulfan, beta",Progesterone receptor,P06401,Endosulfan is an endocrine disruptor and acts as an agonist at the progesterone receptor. (R312)
788,T3D0067,"Endosulfan, beta",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
789,T3D0067,"Endosulfan, beta",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
792,T3D0068,Aroclor 1232,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
793,T3D0068,Aroclor 1232,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
794,T3D0068,Aroclor 1232,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
803,T3D0068,Aroclor 1232,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
805,T3D0070,Benzofluoranthene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
806,T3D0070,Benzofluoranthene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
807,T3D0074,Zinc,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
808,T3D0075,Dimethylarsinic acid,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
809,T3D0075,Dimethylarsinic acid,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
817,T3D0077,Chromium,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
818,T3D0077,Chromium,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
819,T3D0077,Chromium,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
820,T3D0077,Chromium,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
822,T3D0078,Naphthalene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
823,T3D0078,Naphthalene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
824,T3D0081,Aroclor 1240,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
825,T3D0081,Aroclor 1240,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
826,T3D0081,Aroclor 1240,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
835,T3D0081,Aroclor 1240,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
840,T3D0093,Hexachlorobenzene,Uroporphyrinogen decarboxylase,P06132,"Hexachlorobenzene causes porphyria by modifying sulfhydryl groups in the catalytic or substrate-binding sites of uroporphyrinogen decarboxylase. This inhibits uroporphyrinogen decarboxylase, resulting in a deficiency of the decarboxylation of uroporphyrinogen III and accumulation of uroporphyrins in the liver. (R437)"
845,T3D0110,Fluoranthene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
846,T3D0110,Fluoranthene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
847,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
848,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
849,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
850,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
851,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
852,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
853,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
854,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
855,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
856,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
857,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
858,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
859,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
860,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
861,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
862,T3D0115,"Hexachlorocyclohexane, alpha-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
863,T3D0115,"Hexachlorocyclohexane, alpha-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
864,T3D0115,"Hexachlorocyclohexane, alpha-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
865,T3D0115,"Hexachlorocyclohexane, alpha-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
866,T3D0115,"Hexachlorocyclohexane, alpha-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
867,T3D0115,"Hexachlorocyclohexane, alpha-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
868,T3D0115,"Hexachlorocyclohexane, alpha-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
869,T3D0115,"Hexachlorocyclohexane, alpha-",Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
870,T3D0115,"Hexachlorocyclohexane, alpha-",Estrogen-related receptor gamma,P62508,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting estrogen-related receptor gamma. (R188)
871,T3D0115,"Hexachlorocyclohexane, alpha-",Androgen receptor,P10275,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the androgen receptor. (R188)
872,T3D0115,"Hexachlorocyclohexane, alpha-",Progesterone receptor,P06401,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the progesterone receptor. (R188)
874,T3D0123,Methylmercury,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
876,T3D0123,Methylmercury,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
877,T3D0123,Methylmercury,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
878,T3D0123,Methylmercury,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
879,T3D0123,Methylmercury,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
880,T3D0123,Methylmercury,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
881,T3D0123,Methylmercury,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
882,T3D0123,Methylmercury,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
883,T3D0123,Methylmercury,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
884,T3D0123,Methylmercury,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
885,T3D0123,Methylmercury,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
886,T3D0123,Methylmercury,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
887,T3D0123,Methylmercury,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
888,T3D0123,Methylmercury,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
889,T3D0123,Methylmercury,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
890,T3D0123,Methylmercury,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
891,T3D0123,Methylmercury,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
892,T3D0123,Methylmercury,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
893,T3D0123,Methylmercury,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
894,T3D0133,Hydrogen cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
895,T3D0133,Hydrogen cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
896,T3D0133,Hydrogen cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
897,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
898,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
899,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
900,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
901,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
902,T3D0133,Hydrogen cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
903,T3D0133,Hydrogen cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
904,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
905,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
906,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
907,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
908,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
909,T3D0133,Hydrogen cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211) 
912,T3D0133,Hydrogen cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212) 
913,T3D0133,Hydrogen cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212) 
914,T3D0133,Hydrogen cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212) 
915,T3D0133,Hydrogen cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212) 
916,T3D0133,Hydrogen cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212) 
917,T3D0133,Hydrogen cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212) 
918,T3D0133,Hydrogen cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214) 
920,T3D0137,Chrysene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
921,T3D0137,Chrysene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
922,T3D0144,Dicofol,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
923,T3D0144,Dicofol,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
924,T3D0144,Dicofol,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
925,T3D0144,Dicofol,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
926,T3D0144,Dicofol,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
927,T3D0144,Dicofol,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
928,T3D0144,Dicofol,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
929,T3D0144,Dicofol,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
930,T3D0144,Dicofol,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
931,T3D0144,Dicofol,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
932,T3D0144,Dicofol,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
933,T3D0144,Dicofol,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
934,T3D0144,Dicofol,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
935,T3D0144,Dicofol,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
936,T3D0144,Dicofol,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
937,T3D0144,Dicofol,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
938,T3D0144,Dicofol,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
939,T3D0144,Dicofol,Calmodulin,P62158,"Difocol inhibits the ability of calmodulin, a calcium mediator in nerves, to transport calcium ions that are essential for the release of neurotransmitters. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
940,T3D0144,Dicofol,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
942,T3D0144,Dicofol,Androgen receptor,P10275,Difocol is also an endocrine disruptor and binds both the androgen and estrogen receptor. (R966)
943,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
944,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
945,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
946,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
947,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
948,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
949,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
950,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
951,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
952,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit delta,O14764,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
953,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
954,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
955,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit pi,O00591,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
956,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
957,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit rho-2,P28476,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
958,T3D0148,"Hexachlorocyclohexane, technical Grade",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Hexachlorocyclohexane inhibits sodium/potassium-transporting ATPases, reducing the rate of depolarization and increasing the sensitivity of neurons. (R186) "
959,T3D0148,"Hexachlorocyclohexane, technical Grade",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Hexachlorocyclohexane inhibits sodium/potassium-transporting ATPases, reducing the rate of depolarization and increasing the sensitivity of neurons. (R186) "
960,T3D0148,"Hexachlorocyclohexane, technical Grade",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Hexachlorocyclohexane inhibits sodium/potassium-transporting ATPases, reducing the rate of depolarization and increasing the sensitivity of neurons. (R186) "
961,T3D0148,"Hexachlorocyclohexane, technical Grade",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Hexachlorocyclohexane inhibits sodium/potassium-transporting ATPases, reducing the rate of depolarization and increasing the sensitivity of neurons. (R186) "
962,T3D0148,"Hexachlorocyclohexane, technical Grade",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Hexachlorocyclohexane inhibits sodium/potassium-transporting ATPases, reducing the rate of depolarization and increasing the sensitivity of neurons. (R186) "
963,T3D0148,"Hexachlorocyclohexane, technical Grade",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Hexachlorocyclohexane inhibits sodium/potassium-transporting ATPases, reducing the rate of depolarization and increasing the sensitivity of neurons. (R186) "
964,T3D0148,"Hexachlorocyclohexane, technical Grade",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Hexachlorocyclohexane inhibits sodium/potassium-transporting ATPases, reducing the rate of depolarization and increasing the sensitivity of neurons. (R186) "
965,T3D0148,"Hexachlorocyclohexane, technical Grade",Sodium/potassium-transporting ATPase gamma chain,P54710,"Hexachlorocyclohexane inhibits sodium/potassium-transporting ATPases, reducing the rate of depolarization and increasing the sensitivity of neurons. (R186) "
966,T3D0148,"Hexachlorocyclohexane, technical Grade",Estrogen-related receptor gamma,P62508,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting estrogen-related receptor gamma. (R188)
967,T3D0148,"Hexachlorocyclohexane, technical Grade",Androgen receptor,P10275,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the androgen receptor. (R188)
968,T3D0148,"Hexachlorocyclohexane, technical Grade",Progesterone receptor,P06401,Hexachlorocyclohexane acts as an endocrine disruptor by inhibiting the progesterone receptor. (R188)
970,T3D0151,"DDD, O,P'-",Androgen receptor,P10275,DDD is also believed to adversely affect the reproductive system by mimicking endogenous hormones and binding to the estrogen and adrogen receptors. (R153) 
971,T3D0151,"DDD, O,P'-",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
972,T3D0151,"DDD, O,P'-",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
973,T3D0151,"DDD, O,P'-",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
974,T3D0151,"DDD, O,P'-",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
975,T3D0151,"DDD, O,P'-",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
976,T3D0151,"DDD, O,P'-",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
977,T3D0151,"DDD, O,P'-",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
978,T3D0151,"DDD, O,P'-",Sodium/potassium-transporting ATPase gamma chain,P54710,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
979,T3D0151,"DDD, O,P'-",Calcium-transporting ATPase type 2C member 1,P98194,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
980,T3D0151,"DDD, O,P'-",Calcium-transporting ATPase type 2C member 2,O75185,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
981,T3D0151,"DDD, O,P'-",Plasma membrane calcium-transporting ATPase 1,P20020,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
982,T3D0151,"DDD, O,P'-",Plasma membrane calcium-transporting ATPase 2,Q01814,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
983,T3D0151,"DDD, O,P'-",Plasma membrane calcium-transporting ATPase 3,Q16720,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
984,T3D0151,"DDD, O,P'-",Plasma membrane calcium-transporting ATPase 4,P23634,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
985,T3D0151,"DDD, O,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
986,T3D0151,"DDD, O,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
987,T3D0151,"DDD, O,P'-",Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"DDD inhibits neuronal adenosine triphosphatases (ATPases), particularly Na+K+-ATPase, and Ca2+-ATPase which play vital roles in neuronal repolarization. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
988,T3D0151,"DDD, O,P'-",Calmodulin,P62158,"DDD inhibits the ability of calmodulin, a calcium mediator in nerves, to transport calcium ions that are essential for the release of neurotransmitters. This reduces the rate of depolarization and increases the sensitivity of neurons to small stimuli that would not elicit a response in a fully depolarized neuron. (R029) "
989,T3D0151,"DDD, O,P'-",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
990,T3D0151,"DDD, O,P'-",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1014,T3D0158,2-Methylnaphthalene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1015,T3D0158,2-Methylnaphthalene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1017,T3D0161,Acenaphthene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1018,T3D0161,Acenaphthene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1020,T3D0174,"Indeno(1,2,3-cd)pyrene",Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1021,T3D0174,"Indeno(1,2,3-cd)pyrene",Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1022,T3D0215,Chromic acid,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
1023,T3D0215,Chromic acid,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
1024,T3D0215,Chromic acid,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
1025,T3D0215,Chromic acid,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
1026,T3D0223,Arsenic acid,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
1027,T3D0223,Arsenic acid,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
1028,T3D0223,Arsenic acid,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
1029,T3D0223,Arsenic acid,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
1030,T3D0223,Arsenic acid,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
1031,T3D0223,Arsenic acid,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
1032,T3D0223,Arsenic acid,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1033,T3D0223,Arsenic acid,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
1034,T3D0223,Arsenic acid,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
1036,T3D0223,Arsenic acid,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1037,T3D0223,Arsenic acid,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
1038,T3D0223,Arsenic acid,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
1040,T3D0224,Arsenic trioxide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
1041,T3D0224,Arsenic trioxide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
1042,T3D0224,Arsenic trioxide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
1043,T3D0224,Arsenic trioxide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
1044,T3D0224,Arsenic trioxide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
1045,T3D0224,Arsenic trioxide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
1046,T3D0224,Arsenic trioxide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1047,T3D0224,Arsenic trioxide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
1048,T3D0224,Arsenic trioxide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
1050,T3D0224,Arsenic trioxide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1051,T3D0224,Arsenic trioxide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
1052,T3D0224,Arsenic trioxide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
1053,T3D0224,Arsenic trioxide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1055,T3D0226,Benzo[e]pyrene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1056,T3D0226,Benzo[e]pyrene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1057,T3D0234,Arsine,Hemoglobin subunit alpha,P69905,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1058,T3D0234,Arsine,Hemoglobin subunit beta,P68871,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1059,T3D0234,Arsine,Hemoglobin subunit gamma-1,P69891,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1060,T3D0234,Arsine,Hemoglobin subunit gamma-2,P69892,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1061,T3D0234,Arsine,Hemoglobin subunit delta,P02042,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1062,T3D0234,Arsine,Hemoglobin subunit epsilon,P02100,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1063,T3D0234,Arsine,Hemoglobin subunit theta-1,P09105,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1064,T3D0234,Arsine,Hemoglobin subunit zeta,P02008,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1065,T3D0234,Arsine,Catalase,P04040,"Arsine may inhibit catalase, which leads to the accumulation of hydrogen peroxide. This destroys red cell membranes and may contribute to arsine-induced conversion of Fe+2 to Fe+3, which also impairs oxygen transport. (R030)"
1066,T3D0241,Calcium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
1067,T3D0241,Calcium arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
1068,T3D0241,Calcium arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
1069,T3D0241,Calcium arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
1070,T3D0241,Calcium arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
1071,T3D0241,Calcium arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
1072,T3D0241,Calcium arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1073,T3D0241,Calcium arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
1074,T3D0241,Calcium arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
1076,T3D0241,Calcium arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1077,T3D0241,Calcium arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
1078,T3D0241,Calcium arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
1079,T3D0241,Calcium arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1081,T3D0242,Mercuric chloride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1083,T3D0242,Mercuric chloride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1084,T3D0242,Mercuric chloride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1085,T3D0242,Mercuric chloride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1086,T3D0242,Mercuric chloride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1087,T3D0242,Mercuric chloride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1088,T3D0242,Mercuric chloride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1089,T3D0242,Mercuric chloride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1090,T3D0242,Mercuric chloride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1091,T3D0242,Mercuric chloride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1092,T3D0242,Mercuric chloride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1093,T3D0242,Mercuric chloride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1094,T3D0242,Mercuric chloride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1095,T3D0242,Mercuric chloride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1096,T3D0242,Mercuric chloride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1097,T3D0242,Mercuric chloride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1098,T3D0242,Mercuric chloride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1099,T3D0242,Mercuric chloride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1100,T3D0242,Mercuric chloride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1101,T3D0243,Sodium arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
1102,T3D0243,Sodium arsenite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
1103,T3D0243,Sodium arsenite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
1104,T3D0243,Sodium arsenite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
1105,T3D0243,Sodium arsenite,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
1106,T3D0243,Sodium arsenite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
1107,T3D0243,Sodium arsenite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1108,T3D0243,Sodium arsenite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
1109,T3D0243,Sodium arsenite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
1111,T3D0243,Sodium arsenite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1112,T3D0243,Sodium arsenite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
1113,T3D0243,Sodium arsenite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
1114,T3D0243,Sodium arsenite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1116,T3D0246,Phenanthrene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1117,T3D0246,Phenanthrene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1119,T3D0253,Pyrene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1120,T3D0253,Pyrene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1122,T3D0340,Mercury(II) fulminate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1124,T3D0341,Mercury(II) sulfide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1126,T3D0342,Mercury(II) oxide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1128,T3D0343,Mercury(I) chloride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1130,T3D0344,Phenylmercuric acetate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1132,T3D0345,Mercury selenide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1134,T3D0346,Mercury telluride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1136,T3D0347,Mercury cadmium telluride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1138,T3D0348,Mercury(II) acetate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1140,T3D0349,Mercury(I) acetate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1142,T3D0350,Mercury(II) iodide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1144,T3D0351,Mercury(I) iodide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1146,T3D0352,Mercury(I) bromide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1148,T3D0353,Mercury(II) bromide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1150,T3D0354,Mercury(II) nitrate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1152,T3D0355,Mercury(I) nitrate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1153,T3D0356,Mercury(II) thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
1154,T3D0356,Mercury(II) thiocyanate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1156,T3D0357,Mercury(II) sulfate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1158,T3D0358,Mercury(I) sulfate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1160,T3D0360,Methylmercuric chloride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1162,T3D0361,Dimethyl mercury,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1164,T3D0361,Dimethyl mercury,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1165,T3D0361,Dimethyl mercury,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1166,T3D0361,Dimethyl mercury,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1167,T3D0361,Dimethyl mercury,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1168,T3D0361,Dimethyl mercury,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1169,T3D0361,Dimethyl mercury,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1170,T3D0361,Dimethyl mercury,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1171,T3D0361,Dimethyl mercury,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1172,T3D0361,Dimethyl mercury,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1173,T3D0361,Dimethyl mercury,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1174,T3D0361,Dimethyl mercury,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1175,T3D0361,Dimethyl mercury,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1176,T3D0361,Dimethyl mercury,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1177,T3D0361,Dimethyl mercury,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1178,T3D0361,Dimethyl mercury,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1179,T3D0361,Dimethyl mercury,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1180,T3D0361,Dimethyl mercury,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1181,T3D0361,Dimethyl mercury,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1183,T3D0362,Mercuric potassium iodide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1184,T3D0363,Mercury(II) cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
1185,T3D0363,Mercury(II) cyanide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
1186,T3D0616,Methiochlor,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1187,T3D0616,Methiochlor,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1188,T3D0616,Methiochlor,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1189,T3D0616,Methiochlor,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1190,T3D0616,Methiochlor,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1191,T3D0616,Methiochlor,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1192,T3D0616,Methiochlor,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1193,T3D0616,Methiochlor,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1194,T3D0616,Methiochlor,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1195,T3D0616,Methiochlor,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1196,T3D0616,Methiochlor,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1197,T3D0616,Methiochlor,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1198,T3D0616,Methiochlor,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1199,T3D0616,Methiochlor,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1200,T3D0616,Methiochlor,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1201,T3D0616,Methiochlor,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1202,T3D0616,Methiochlor,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1203,T3D0617,Chlorbenzylate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1204,T3D0617,Chlorbenzylate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1205,T3D0617,Chlorbenzylate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1206,T3D0617,Chlorbenzylate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1207,T3D0617,Chlorbenzylate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1208,T3D0617,Chlorbenzylate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1209,T3D0617,Chlorbenzylate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1210,T3D0617,Chlorbenzylate,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1211,T3D0617,Chlorbenzylate,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1212,T3D0617,Chlorbenzylate,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1213,T3D0617,Chlorbenzylate,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1214,T3D0617,Chlorbenzylate,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1215,T3D0617,Chlorbenzylate,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1216,T3D0617,Chlorbenzylate,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1217,T3D0617,Chlorbenzylate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1218,T3D0617,Chlorbenzylate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1219,T3D0617,Chlorbenzylate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1220,T3D0628,1-Methylnaphthalene,Cellular tumor antigen p53,P04637,1-Methylnaphthalene binds to cellular tumor antigen p53.
1221,T3D0628,1-Methylnaphthalene,Aryl hydrocarbon receptor,P35869,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1222,T3D0628,1-Methylnaphthalene,Glycine N-methyltransferase,Q14749,"Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
1225,T3D0752,Chloral hydrate,Alcohol dehydrogenase 1A,P07327,
1226,T3D0752,Chloral hydrate,Alcohol dehydrogenase 1B,P00325,
1227,T3D0752,Chloral hydrate,Alcohol dehydrogenase 1C,P00326,
1228,T3D0752,Chloral hydrate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,
1229,T3D0752,Chloral hydrate,Alcohol dehydrogenase class-3,P11766,
1230,T3D0752,Chloral hydrate,Alcohol dehydrogenase 4,P08319,
1231,T3D0752,Chloral hydrate,Alcohol dehydrogenase 6,P28332,
1248,T3D0123,Methylmercury,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1249,T3D0123,Methylmercury,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1250,T3D0123,Methylmercury,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1251,T3D0123,Methylmercury,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1252,T3D0123,Methylmercury,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1253,T3D0123,Methylmercury,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1254,T3D0123,Methylmercury,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1255,T3D0123,Methylmercury,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1256,T3D0123,Methylmercury,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1257,T3D0123,Methylmercury,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1258,T3D0123,Methylmercury,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1259,T3D0123,Methylmercury,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1260,T3D0123,Methylmercury,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1261,T3D0123,Methylmercury,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1262,T3D0242,Mercuric chloride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1263,T3D0242,Mercuric chloride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1264,T3D0242,Mercuric chloride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1265,T3D0242,Mercuric chloride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1266,T3D0242,Mercuric chloride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1267,T3D0242,Mercuric chloride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1268,T3D0242,Mercuric chloride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1269,T3D0242,Mercuric chloride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1270,T3D0242,Mercuric chloride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1271,T3D0242,Mercuric chloride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1272,T3D0242,Mercuric chloride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1273,T3D0242,Mercuric chloride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1274,T3D0242,Mercuric chloride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1275,T3D0242,Mercuric chloride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1276,T3D0361,Dimethyl mercury,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1277,T3D0361,Dimethyl mercury,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1278,T3D0361,Dimethyl mercury,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
1279,T3D0361,Dimethyl mercury,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1280,T3D0361,Dimethyl mercury,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1281,T3D0361,Dimethyl mercury,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1282,T3D0361,Dimethyl mercury,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1283,T3D0361,Dimethyl mercury,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1284,T3D0361,Dimethyl mercury,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1285,T3D0361,Dimethyl mercury,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1286,T3D0361,Dimethyl mercury,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1287,T3D0361,Dimethyl mercury,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1288,T3D0361,Dimethyl mercury,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1289,T3D0361,Dimethyl mercury,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
1290,T3D0006,Benzene,Tubulin alpha-1A chain,Q71U36,Direct binding of tubulin leads to protein damage. (R016)
1291,T3D0006,Benzene,Tubulin alpha-1C chain,Q9BQE3,Direct binding of tubulin leads to protein damage. (R016)
1292,T3D0006,Benzene,Tubulin alpha-3E chain,Q6PEY2,Direct binding of tubulin leads to protein damage. (R016)
1293,T3D0006,Benzene,Tubulin alpha-8 chain,Q9NY65,Direct binding of tubulin leads to protein damage. (R016)
1294,T3D0006,Benzene,Tubulin beta-1 chain,Q9H4B7,Direct binding of tubulin leads to protein damage. (R016)
1295,T3D0006,Benzene,Tubulin beta-2B chain,Q9BVA1,Direct binding of tubulin leads to protein damage. (R016)
1296,T3D0006,Benzene,Tubulin beta-6 chain,Q9BUF5,Direct binding of tubulin leads to protein damage. (R016)
1297,T3D0006,Benzene,Tubulin beta-8 chain,Q3ZCM7,Direct binding of tubulin leads to protein damage. (R016)
1298,T3D0006,Benzene,Tubulin delta chain,Q9UJT1,Direct binding of tubulin leads to protein damage. (R016)
1299,T3D0006,Benzene,Tubulin epsilon chain,Q9UJT0,Direct binding of tubulin leads to protein damage. (R016)
1300,T3D0006,Benzene,Tubulin gamma-2 chain,Q9NRH3,Direct binding of tubulin leads to protein damage. (R016)
1301,T3D0053,Nickel,Histone H3.2,Q71DI3,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1302,T3D0006,Benzene,Histone H3.2,Q71DI3,Direct binding of histone leads to protein damage. (R016)
1303,T3D0006,Benzene,Ribonucleoside-diphosphate reductase subunit M2 B,Q7LG56,Benzene binding of DNA associated proteins leads to mutagenic effects. (R016)
1305,T3D0007,Cadmium,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
1306,T3D0007,Cadmium,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
1307,T3D0006,Benzene,"DNA polymerase subunit gamma-2, mitochondrial",Q9UHN1,Benzene binding of DNA associated proteins leads to mutagenic effects. (R016)
1308,T3D0011,Chloroform,Potassium voltage-gated channel subfamily H member 6,Q9H252,"Chloroform has been shown to block HERG potassium channels, causing cardiac arrest. (R070)"
1309,T3D0011,Chloroform,Potassium voltage-gated channel subfamily H member 7,Q9NS40,"Chloroform has been shown to block HERG potassium channels, causing cardiac arrest. (R070)"
1310,T3D0053,Nickel,Calcineurin subunit B isoform 2,Q96LZ3,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
1311,T3D0007,Cadmium,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
1312,T3D0002,Lead,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
1313,T3D0071,Toluene,Sodium channel subunit beta-1,Q07699,"Toluene binds to cardiac Na+ channels in the open state and unbinds either when channels move between inactivated states or from an inactivated to a closed state. The use- and frequency-dependent block of Na+ by toluene might be responsible, at least in part, for its arrhythmogenic effect. (R201)"
1314,T3D0071,Toluene,Sodium channel subunit beta-2,O60939,"Toluene binds to cardiac Na+ channels in the open state and unbinds either when channels move between inactivated states or from an inactivated to a closed state. The use- and frequency-dependent block of Na+ by toluene might be responsible, at least in part, for its arrhythmogenic effect. (R201)"
1315,T3D0071,Toluene,Sodium channel subunit beta-3,Q9NY72,"Toluene binds to cardiac Na+ channels in the open state and unbinds either when channels move between inactivated states or from an inactivated to a closed state. The use- and frequency-dependent block of Na+ by toluene might be responsible, at least in part, for its arrhythmogenic effect. (R201)"
1316,T3D0071,Toluene,Sodium channel subunit beta-4,Q8IWT1,"Toluene binds to cardiac Na+ channels in the open state and unbinds either when channels move between inactivated states or from an inactivated to a closed state. The use- and frequency-dependent block of Na+ by toluene might be responsible, at least in part, for its arrhythmogenic effect. (R201)"
1317,T3D0028,Cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1318,T3D0028,Cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1319,T3D0028,Cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1320,T3D0028,Cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1321,T3D0133,Hydrogen cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1322,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1323,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1324,T3D0133,Hydrogen cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1325,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1326,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1327,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1328,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1329,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1330,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1331,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1332,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1333,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1334,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1335,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1336,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1337,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1338,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1339,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1340,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
1341,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
1342,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
1343,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1344,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1345,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1346,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1347,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1348,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1349,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1350,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1351,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1352,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1353,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1354,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1355,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1356,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1357,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1358,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1359,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1360,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1362,T3D0234,Arsine,Hemoglobin subunit mu,Q6B0K9,"Arsine enters the bloodstream and crosses the alveolo-capillary membrane into red blood cells. Here it preferentially binds to hemoglobin and is oxidized to an arsenic dihydride intermediate and elemental arsenic, both of which are hemolytic agents. Arsine also depletes the reduced glutathione content of the red blood cells, resulting in the oxidation of sulfhydryl groups in hemoglobin and red cell membranes. These effects produce membrane instability, resulting in hemolysis. (R030)"
1371,T3D0243,Sodium arsenite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1372,T3D0243,Sodium arsenite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1373,T3D0223,Arsenic acid,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1374,T3D0223,Arsenic acid,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1375,T3D0224,Arsenic trioxide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1376,T3D0224,Arsenic trioxide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1377,T3D0241,Calcium arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1378,T3D0241,Calcium arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1379,T3D0001,Arsenic,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1380,T3D0001,Arsenic,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
1381,T3D0012,"DDT, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1382,T3D0012,"DDT, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1383,T3D0021,"DDE, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1384,T3D0021,"DDE, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1385,T3D0025,"DDD, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1386,T3D0025,"DDD, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1387,T3D0050,"DDT, O,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1388,T3D0050,"DDT, O,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1389,T3D0144,Dicofol,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1390,T3D0144,Dicofol,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1391,T3D0151,"DDD, O,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1392,T3D0151,"DDD, O,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1395,T3D0061,Methoxychlor,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1396,T3D0061,Methoxychlor,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1410,T3D0028,Cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212) 
1411,T3D0133,Hydrogen cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212) 
1412,T3D0012,"DDT, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1413,T3D0012,"DDT, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1414,T3D0144,Dicofol,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1415,T3D0144,Dicofol,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1418,T3D0021,"DDE, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1419,T3D0021,"DDE, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1420,T3D0025,"DDD, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1421,T3D0025,"DDD, P,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1422,T3D0050,"DDT, O,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1423,T3D0050,"DDT, O,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1424,T3D0151,"DDD, O,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1425,T3D0151,"DDD, O,P'-",Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1426,T3D0061,Methoxychlor,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1427,T3D0061,Methoxychlor,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1428,T3D0616,Methiochlor,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,"Methiochlor inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1429,T3D0616,Methiochlor,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,"Methiochlor inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1430,T3D0616,Methiochlor,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,"Methiochlor inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1431,T3D0616,Methiochlor,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,"Methiochlor inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1432,T3D0617,Chlorbenzylate,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1,O60741,Chlorobenzilate binds to Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1.
1433,T3D0617,Chlorbenzylate,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2,Q9UL51,Chlorobenzilate binds to Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2.
1434,T3D0617,Chlorbenzylate,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3,Q9P1Z3 ,Chlorobenzilate binds to Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3.
1435,T3D0617,Chlorbenzylate,Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4,Q9Y3Q4,Chlorobenzilate binds to Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4.
1436,T3D0001,Arsenic,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
1437,T3D0026,Benzidine,Hemoglobin subunit alpha,P69905,Benzidine has been shown to bind hemoglobin. (R169)
1438,T3D0026,Benzidine,Hemoglobin subunit beta,P68871,Benzidine has been shown to bind hemoglobin. (R169)
1439,T3D0026,Benzidine,Hemoglobin subunit delta,P02042,Benzidine has been shown to bind hemoglobin. (R169)
1440,T3D0026,Benzidine,Hemoglobin subunit epsilon,P02100,Benzidine has been shown to bind hemoglobin. (R169)
1441,T3D0026,Benzidine,Hemoglobin subunit gamma-1,P69891,Benzidine has been shown to bind hemoglobin. (R169)
1442,T3D0026,Benzidine,Hemoglobin subunit gamma-2,P69892,Benzidine has been shown to bind hemoglobin. (R169)
1443,T3D0026,Benzidine,Hemoglobin subunit mu,Q6B0K9,Benzidine has been shown to bind hemoglobin. (R169)
1444,T3D0026,Benzidine,Hemoglobin subunit theta-1,P09105,Benzidine has been shown to bind hemoglobin. (R169)
1445,T3D0026,Benzidine,Hemoglobin subunit zeta,P02008,Benzidine has been shown to bind hemoglobin. (R169)
1457,T3D0001,Arsenic,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1458,T3D0001,Arsenic,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1459,T3D0001,Arsenic,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1460,T3D0001,Arsenic,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1461,T3D0001,Arsenic,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1462,T3D0001,Arsenic,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1463,T3D0001,Arsenic,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1464,T3D0001,Arsenic,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1465,T3D0001,Arsenic,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1466,T3D0001,Arsenic,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1467,T3D0001,Arsenic,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1468,T3D0001,Arsenic,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1469,T3D0001,Arsenic,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1470,T3D0001,Arsenic,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1471,T3D0001,Arsenic,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1472,T3D0001,Arsenic,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
1473,T3D0001,Arsenic,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
1474,T3D0001,Arsenic,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
1475,T3D0001,Arsenic,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
1477,T3D0001,Arsenic,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
1478,T3D0001,Arsenic,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
1479,T3D0005,Polychlorinated biphenyls,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
1480,T3D0005,Polychlorinated biphenyls,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
1481,T3D0005,Polychlorinated biphenyls,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1482,T3D0013,Aroclor 1254,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
1483,T3D0013,Aroclor 1254,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
1484,T3D0013,Aroclor 1254,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1485,T3D0014,Aroclor 1260,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
1486,T3D0014,Aroclor 1260,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1487,T3D0014,Aroclor 1260,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
1488,T3D0016,Trichloroethylene,"[Pyruvate dehydrogenase [lipoamide]] kinase isozyme 3, mitochondrial",Q15120,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Dichloroacetic acid is known to inhibit pyruvate dehydrogenase kinase. (R160)"
1489,T3D0016,Trichloroethylene,"[Pyruvate dehydrogenase [lipoamide]] kinase isozyme 4, mitochondrial",Q16654,"The toxic and carcinogenic effects of trichloroethylene are believed to be cause mainly by its metabolites, including trichloroacetic acid, dichloroacetic acid, and chloral hydrate. The nephrotoxicity and nephrocarcinogenicity of TRI have been attributed to glutathione conjunction, which forms reactive, sulfur-containing metabolites. Dichloroacetic acid is known to inhibit pyruvate dehydrogenase kinase. (R160)"
1490,T3D0020,Chlordane,Cytochrome P450 2B6,P20813,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1492,T3D0020,Chlordane,Cytochrome P450 3A4,P08684,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1493,T3D0020,Chlordane,Cytochrome P450 3A43,Q9HB55,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1494,T3D0020,Chlordane,Cytochrome P450 3A5,P20815,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1495,T3D0020,Chlordane,Cytochrome P450 3A7,P24462,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1496,T3D0020,Chlordane,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Chlordane inhibit alkaline phosphatases in hepatic and renal tissues. (R206)
1497,T3D0019,"Phosphorus, white",Leptin,P41159,Phosphorus may enhance deposition of calcium by activating leptin. (R207)
1499,T3D0019,"Phosphorus, white",Sodium-dependent phosphate transporter 1,Q8WUM9,Phosphorus may enhance deposition of calcium by activating sodium-dependent phosphate transporter 1. (R207)
1501,T3D0022,Hexachlorobutadiene,Apolipoprotein D,P05090,The binding of hexachlorobutadiene to alpha 2u-globulin is believed to be an important factor in its nephrotoxicity. (R167)
1502,T3D0027,Aroclor 1248,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1503,T3D0027,Aroclor 1248,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012) 
1504,T3D0027,Aroclor 1248,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012) 
1506,T3D0029,Aroclor 1242,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012) 
1508,T3D0029,Aroclor 1242,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012) 
1510,T3D0029,Aroclor 1242,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1511,T3D0028,Cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
1512,T3D0028,Cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
1514,T3D0028,Cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
1516,T3D0028,Cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213) 
1517,T3D0028,Cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213) 
1518,T3D0028,Cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213) 
1519,T3D0028,Cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213) 
1520,T3D0028,Cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
1521,T3D0031,Toxaphene,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1522,T3D0031,Toxaphene,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1523,T3D0031,Toxaphene,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1524,T3D0031,Toxaphene,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1525,T3D0031,Toxaphene,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1526,T3D0031,Toxaphene,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1527,T3D0031,Toxaphene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1528,T3D0031,Toxaphene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1529,T3D0031,Toxaphene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1530,T3D0031,Toxaphene,Adenylate cyclase type 1,Q08828,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1531,T3D0031,Toxaphene,Adenylate cyclase type 10,Q96PN6,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1532,T3D0031,Toxaphene,Adenylate cyclase type 2,Q08462,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1533,T3D0031,Toxaphene,Adenylate cyclase type 3,O60266,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1534,T3D0031,Toxaphene,Adenylate cyclase type 4,Q8NFM4,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1535,T3D0031,Toxaphene,Adenylate cyclase type 5,O95622,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1536,T3D0031,Toxaphene,Adenylate cyclase type 6,O43306,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1537,T3D0031,Toxaphene,Adenylate cyclase type 7,P51828,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1538,T3D0031,Toxaphene,Adenylate cyclase type 8,P40145,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1539,T3D0031,Toxaphene,Adenylate cyclase type 9,O60503,"Toxaphene inhibits adenylate cyclase, which affects the sensitivity of the nervous system by altering calcium transport across cell membranes. (R216)"
1540,T3D0031,Toxaphene,Acetylcholinesterase,P22303,"Toxapehene inhibits acetylcholinesterase, which affects the sensitivity of the nervous system. (R217)"
1541,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1542,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1543,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1544,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1545,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1546,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1547,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1548,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1549,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1550,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1551,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1552,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1553,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1554,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1555,T3D0034,Heptachlor,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1556,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1557,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1558,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1559,T3D0035,"1,2-Dibromoethane",Serum albumin,P02768,"1,2-Dibromoethane binds to serum albumin. (R223)"
1561,T3D0037,Acrolein,Inhibitor of nuclear factor kappa-B kinase subunit alpha,O15111,"Perturbation of inflammatory responses in bronchial epithelial cells was demonstrated by direct action of acrolein on the inhibitor of nuclear factor kappa-B (IκB) kinase, which inhibits activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) transcription factor and suppresses interleukin 8 (IL-8) production. (R223)"
1562,T3D0037,Acrolein,Inhibitor of nuclear factor kappa-B kinase subunit beta,O14920,"Perturbation of inflammatory responses in bronchial epithelial cells was demonstrated by direct action of acrolein on the inhibitor of nuclear factor kappa-B (IκB) kinase, which inhibits activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) transcription factor and suppresses interleukin 8 (IL-8) production. (R223)"
1563,T3D0037,Acrolein,Inhibitor of nuclear factor kappa-B kinase subunit epsilon,Q14164,"Perturbation of inflammatory responses in bronchial epithelial cells was demonstrated by direct action of acrolein on the inhibitor of nuclear factor kappa-B (IκB) kinase, which inhibits activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) transcription factor and suppresses interleukin 8 (IL-8) production. (R223)"
1564,T3D0037,Acrolein,Thioredoxin,P10599,"Acrolein inhibits thioredoxin, which disrupts the cellular thiol redox balance necessary for cell survival. (R226)"
1565,T3D0037,Acrolein,"Thioredoxin, mitochondrial",Q99757,"Acrolein inhibits thioredoxin, which disrupts the cellular thiol redox balance necessary for cell survival. (R226)"
1566,T3D0037,Acrolein,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Acrolein inhibits thioredoxin reductase, which disrupts the cellular thiol redox balance necessary for cell survival. (R226)"
1567,T3D0037,Acrolein,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Acrolein inhibits thioredoxin reductase, which disrupts the cellular thiol redox balance necessary for cell survival. (R226)"
1568,T3D0037,Acrolein,Thioredoxin reductase 3,Q86VQ6,"Acrolein inhibits thioredoxin reductase, which disrupts the cellular thiol redox balance necessary for cell survival. (R226)"
1569,T3D0037,Acrolein,Apolipoprotein A-I,P02647,Acrolein interferes with normal reverse cholesterol transport by high density lipoprotein (HDL) by modifying specific sites in apolipoprotein A-I. (R228)
1570,T3D0037,Acrolein,Aldehyde dehydrogenase 1A3,P47895,Acrolein inhibits aldehyde dehydrogenases. (R227)
1571,T3D0037,Acrolein,Fatty aldehyde dehydrogenase,P51648,Acrolein inhibits aldehyde dehydrogenases. (R227)
1572,T3D0037,Acrolein,"Aldehyde dehydrogenase, dimeric NADP-preferring",P30838,Acrolein inhibits aldehyde dehydrogenases. (R227)
1573,T3D0037,Acrolein,Retinal dehydrogenase 1,P00352,Acrolein inhibits aldehyde dehydrogenases. (R227)
1574,T3D0037,Acrolein,Retinal dehydrogenase 2,O94788,Acrolein inhibits aldehyde dehydrogenases. (R227)
1575,T3D0037,Acrolein,Aldehyde dehydrogenase family 3 member B1,P43353,Acrolein inhibits aldehyde dehydrogenases. (R227)
1576,T3D0037,Acrolein,Aldehyde dehydrogenase family 3 member B2,P48448,Acrolein inhibits aldehyde dehydrogenases. (R227)
1577,T3D0037,Acrolein,"Aldehyde dehydrogenase X, mitochondrial",P30837,Acrolein inhibits aldehyde dehydrogenases. (R227)
1578,T3D0037,Acrolein,10-formyltetrahydrofolate dehydrogenase,O75891,Acrolein inhibits aldehyde dehydrogenases. (R227)
1579,T3D0037,Acrolein,Probable 10-formyltetrahydrofolate dehydrogenase ALDH1L2,Q3SY69,Acrolein inhibits aldehyde dehydrogenases. (R227)
1580,T3D0037,Acrolein,Transient receptor potential cation channel subfamily A member 1,O75762,"Acrolein activates the transient receptor potential cation channel, causing acute pain. (R229)"
1581,T3D0038,Disulfoton,Acetylcholinesterase,P22303,"The toxic metabolites of disulfoton, mainly disulfoton sulfoxide, disulfoton sulfone, demeton S-sulfoxide and demeton S-sulfone, inhibit acetylcholinesterase in nervous tissue. The inhibition of acetylcholinesterase results in the accumulation of acetylcholine at the muscarinic and nicotinic cholinergic receptors of nerve synapses, which causes an overstimulation of cholinergic nerves and effector organs. (R230)"
1583,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit alpha,P69905,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1584,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit beta,P68871,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1585,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit delta,P02042,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1586,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit epsilon,P02100,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1587,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit gamma-1,P69891,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1588,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit gamma-2,P69892,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1589,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit mu,Q6B0K9,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1590,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit theta-1,P09105,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1591,T3D0040,"3,3'-Dichlorobenzidine",Hemoglobin subunit zeta,P02008,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
1592,T3D0040,"3,3'-Dichlorobenzidine",Aryl hydrocarbon receptor,P35869,"3,3’-Dichlorobenzidine acts on the aryl hydrocarbon receptor to induce the activity of cytochrome p-450 enzymes, which metabolize 3,3’-dichlorobenzidine, along with other polyhalogenated aromatics, into their toxic intermediates. (R234)"
1593,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1594,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1595,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1596,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1597,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1598,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1599,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1600,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1601,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1602,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit delta,O14764,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1603,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1604,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1605,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1606,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit pi,O00591,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1607,T3D0046,Heptachlor epoxide,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1608,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1609,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1610,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1611,T3D0048,Aroclor 1221,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
1612,T3D0051,Aroclor 1016,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
1613,T3D0048,Aroclor 1221,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1614,T3D0051,Aroclor 1016,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1615,T3D0048,Aroclor 1221,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
1616,T3D0051,Aroclor 1016,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
1617,T3D0042,Beryllium,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
1618,T3D0042,Beryllium,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
1619,T3D0042,Beryllium,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
1620,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial",P49821,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1621,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial",P19404,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1622,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] flavoprotein 3, mitochondrial",P56181,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1623,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial",O75306,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1624,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial",O75489,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1625,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial",O43181,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1626,T3D0044,"1,2-Dibromo-3-chloropropane",NADH dehydrogenase [ubiquinone] iron-sulfur protein 5,O43920,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1627,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial",O75380,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1628,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial",O75251,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1629,T3D0044,"1,2-Dibromo-3-chloropropane","NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial",O00217,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1630,T3D0044,"1,2-Dibromo-3-chloropropane","NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial",P28331,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1631,T3D0044,"1,2-Dibromo-3-chloropropane",NADH-ubiquinone oxidoreductase chain 1,P03886,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1632,T3D0044,"1,2-Dibromo-3-chloropropane",NADH-ubiquinone oxidoreductase chain 2,P03891,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1633,T3D0044,"1,2-Dibromo-3-chloropropane",NADH-ubiquinone oxidoreductase chain 3,P03897,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1634,T3D0044,"1,2-Dibromo-3-chloropropane",NADH-ubiquinone oxidoreductase chain 4,P03905,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1635,T3D0044,"1,2-Dibromo-3-chloropropane",NADH-ubiquinone oxidoreductase chain 4L,P03901,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1636,T3D0044,"1,2-Dibromo-3-chloropropane",NADH-ubiquinone oxidoreductase chain 5,P03915,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1637,T3D0044,"1,2-Dibromo-3-chloropropane",NADH-ubiquinone oxidoreductase chain 6,P03923,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1638,T3D0045,Pentachlorophenol,Sulfotransferase 1A1,P50225,Pentachlorophenol prevents sulfation by inhibiting phenol-sulfotransferases. (R241)
1639,T3D0045,Pentachlorophenol,Sulfotransferase 1A2,P50226,Pentachlorophenol prevents sulfation by inhibiting phenol-sulfotransferases. (R241)
1640,T3D0045,Pentachlorophenol,Sulfotransferase 1A3/1A4,P50224,Pentachlorophenol prevents sulfation by inhibiting phenol-sulfotransferases. (R241)
1641,T3D0045,Pentachlorophenol,Acetylcholinesterase,P22303,Pentachlorophenol inhibits acetylcholinesterase in erythrocyte membranes. (R242)
1642,T3D0045,Pentachlorophenol,Transthyretin,P02766,Pentachlorophenol competes with thyroxine for uptake into cerebrospinal fluid at the T4 binding site of transthyretin. (R239)
1643,T3D0045,Pentachlorophenol,Carnitine O-acetyltransferase,P43155,Pentachlorophenol inhibits O-acetyltransferases. (R243)
1644,T3D0045,Pentachlorophenol,Choline O-acetyltransferase,P28329,Pentachlorophenol inhibits O-acetyltransferases. (R243)
1645,T3D0045,Pentachlorophenol,Lysophosphatidylcholine acyltransferase 2,Q7L5N7,Pentachlorophenol inhibits O-acetyltransferases. (R243)
1646,T3D0045,Pentachlorophenol,Thyroxine-binding globulin,P05543,"Pentachlorophenol causes adverse effects on thyroid homeostasis, decreasing serum thyroxine by competing for serum protein thyroxine binding sites. (R239)"
1647,T3D0045,Pentachlorophenol,1-acylglycerophosphocholine O-acyltransferase 1,Q8NF37,Pentachlorophenol inhibits O-acetyltransferases. (R243)
1648,T3D0045,Pentachlorophenol,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1649,T3D0045,Pentachlorophenol,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1650,T3D0045,Pentachlorophenol,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1651,T3D0045,Pentachlorophenol,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1652,T3D0045,Pentachlorophenol,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1653,T3D0045,Pentachlorophenol,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1654,T3D0045,Pentachlorophenol,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1655,T3D0045,Pentachlorophenol,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1656,T3D0045,Pentachlorophenol,Potassium-transporting ATPase alpha chain 1,P20648,"Pentachlorophenol inhibits mitochondrial ATP-ase activity, preventing the the formation of ATP and the release of energy to the cell from the breakdown of ATP to ADP. (R244)"
1657,T3D0045,Pentachlorophenol,Potassium-transporting ATPase alpha chain 2,P54707,"Pentachlorophenol inhibits mitochondrial ATP-ase activity, preventing the the formation of ATP and the release of energy to the cell from the breakdown of ATP to ADP. (R244)"
1658,T3D0045,Pentachlorophenol,Potassium-transporting ATPase subunit beta,P51164,"Pentachlorophenol inhibits mitochondrial ATP-ase activity, preventing the the formation of ATP and the release of energy to the cell from the breakdown of ATP to ADP. (R244)"
1659,T3D0047,Carbon tetrachloride,Cytochrome P450 2E1,P05181,"Metabolism of carbon tetrachloride by CYP2E1 may result in the destruction of the enzyme during the metabolic process, either by direct attack of radicals on the cytochrome(s) or highly localized lipid peroxidation resulting in detachment of P-450 proteins from the microsomal membranes. (R245)"
1664,T3D0037,Acrolein,"Succinate-semialdehyde dehydrogenase, mitochondrial",P51649,Acrolein inhibits aldehyde dehydrogenases. (R227)
1670,T3D0001,Arsenic,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
1671,T3D0001,Arsenic,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
1672,T3D0001,Arsenic,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
1673,T3D0001,Arsenic,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
1676,T3D0053,Nickel,Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform,Q08209,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
1677,T3D0053,Nickel,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
1678,T3D0053,Nickel,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
1679,T3D0049,Cobalt,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
1680,T3D0049,Cobalt,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
1681,T3D0028,Cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
1682,T3D0028,Cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212) 
1683,T3D0028,Cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
1684,T3D0017,Dieldrin,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1685,T3D0024,Aldrin,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1686,T3D0031,Toxaphene,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1687,T3D0032,"Hexachlorocyclohexane, gamma-",Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1688,T3D0034,Heptachlor,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1689,T3D0036,"Hexachlorocyclohexane, beta-",Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1690,T3D0041,Endrin,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1691,T3D0043,"Hexachlorocyclohexane, delta-",Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1692,T3D0046,Heptachlor epoxide,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1693,T3D0054,Endosulfan,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1694,T3D0055,Endosulfan sulfate,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Endosulfan sulfate antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1695,T3D0057,"Endosulfan, alpha",Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
1696,T3D0037,Acrolein,NF-kappa-B essential modulator,Q9Y6K9,"Perturbation of inflammatory responses in bronchial epithelial cells was demonstrated by direct action of acrolein on the inhibitor of nuclear factor kappa-B (IκB) kinase, which inhibits activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) transcription factor and suppresses interleukin 8 (IL-8) production. (R223)"
1697,T3D0053,Nickel,Protamine-3,Q9NNZ6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1698,T3D0053,Nickel,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1700,T3D0082,"2,4,6-Trinitrotoluene","Nitric-oxide synthase, endothelial",P29474,"2,4,6-Trinitrotoluene is a competitive inhibitor with respect to NADPH and a noncompetitive inhibitor with respect to l-arginine. It binds to the P450 reductase domain of endothelial nitric oxide synthase and suppresses l-citrulline formation by shunting electrons away from the normal catalytic pathway. (R296)"
1702,T3D0001,Arsenic,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1703,T3D0001,Arsenic,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1706,T3D0006,Benzene,Tubulin alpha chain-like 3,A6NHL2,Direct binding of tubulin leads to protein damage. (R016)
1707,T3D0006,Benzene,Tubulin beta-8 chain B,A6NNZ2,Direct binding of tubulin leads to protein damage. (R016)
1708,T3D0045,Pentachlorophenol,X/potassium-transporting ATPase subunit beta-m,Q9UN42,"Pentachlorophenol inhibits mitochondrial ATP-ase activity, preventing the the formation of ATP and the release of energy to the cell from the breakdown of ATP to ADP. (R244)"
1709,T3D0004,Vinyl chloride,Ig gamma-1 chain C region,P01857,"Vinyl chloride poisoning exhibits many of the characteristics of autoimmune diseases. This is believed to be the result of a reactive vinyl chloride intermediate metabolite binding to an immunoglobulin G (IgG), altering the protein and initiating an immune response. (R010)"
1710,T3D0004,Vinyl chloride,Ig gamma-2 chain C region,P01859,"Vinyl chloride poisoning exhibits many of the characteristics of autoimmune diseases. This is believed to be the result of a reactive vinyl chloride intermediate metabolite binding to an immunoglobulin G (IgG), altering the protein and initiating an immune response. (R010)"
1711,T3D0004,Vinyl chloride,Ig gamma-3 chain C region,P01860,"Vinyl chloride poisoning exhibits many of the characteristics of autoimmune diseases. This is believed to be the result of a reactive vinyl chloride intermediate metabolite binding to an immunoglobulin G (IgG), altering the protein and initiating an immune response. (R010)"
1712,T3D0004,Vinyl chloride,Ig gamma-4 chain C region,P01861,"Vinyl chloride poisoning exhibits many of the characteristics of autoimmune diseases. This is believed to be the result of a reactive vinyl chloride intermediate metabolite binding to an immunoglobulin G (IgG), altering the protein and initiating an immune response. (R010)"
1713,T3D0012,"DDT, P,P'-",Sodium channel protein type 1 subunit alpha,P35498,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1714,T3D0012,"DDT, P,P'-",Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1715,T3D0012,"DDT, P,P'-",Sodium channel protein type 11 subunit alpha,Q9UI33,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1716,T3D0012,"DDT, P,P'-",Sodium channel protein type 2 subunit alpha,Q99250,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1717,T3D0012,"DDT, P,P'-",Sodium channel protein type 3 subunit alpha,Q9NY46,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1718,T3D0012,"DDT, P,P'-",Sodium channel protein type 4 subunit alpha,P35499,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1719,T3D0012,"DDT, P,P'-",Sodium channel protein type 7 subunit alpha,Q01118,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1720,T3D0012,"DDT, P,P'-",Sodium channel protein type 8 subunit alpha,Q9UQD0,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1721,T3D0012,"DDT, P,P'-",Sodium channel protein type 5 subunit alpha,Q14524,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1722,T3D0012,"DDT, P,P'-",Sodium channel protein type 9 subunit alpha,Q15858,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1723,T3D0061,Methoxychlor,Sodium channel protein type 1 subunit alpha,P35498,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1724,T3D0061,Methoxychlor,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1725,T3D0061,Methoxychlor,Sodium channel protein type 11 subunit alpha,Q9UI33,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1726,T3D0061,Methoxychlor,Sodium channel protein type 2 subunit alpha,Q99250,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1727,T3D0061,Methoxychlor,Sodium channel protein type 3 subunit alpha,Q9NY46,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1728,T3D0061,Methoxychlor,Sodium channel protein type 4 subunit alpha,P35499,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1729,T3D0061,Methoxychlor,Sodium channel protein type 5 subunit alpha,Q14524,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1730,T3D0061,Methoxychlor,Sodium channel protein type 7 subunit alpha,Q01118,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1731,T3D0061,Methoxychlor,Sodium channel protein type 8 subunit alpha,Q9UQD0,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1732,T3D0061,Methoxychlor,Sodium channel protein type 9 subunit alpha,Q15858,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1733,T3D0021,"DDE, P,P'-",Sodium channel protein type 1 subunit alpha,P35498,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1734,T3D0021,"DDE, P,P'-",Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1735,T3D0021,"DDE, P,P'-",Sodium channel protein type 11 subunit alpha,Q9UI33,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1736,T3D0021,"DDE, P,P'-",Sodium channel protein type 2 subunit alpha,Q99250,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1737,T3D0021,"DDE, P,P'-",Sodium channel protein type 3 subunit alpha,Q9NY46,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1738,T3D0021,"DDE, P,P'-",Sodium channel protein type 4 subunit alpha,P35499,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1739,T3D0021,"DDE, P,P'-",Sodium channel protein type 5 subunit alpha,Q14524,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1740,T3D0021,"DDE, P,P'-",Sodium channel protein type 7 subunit alpha,Q01118,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1741,T3D0021,"DDE, P,P'-",Sodium channel protein type 8 subunit alpha,Q9UQD0,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1742,T3D0021,"DDE, P,P'-",Sodium channel protein type 9 subunit alpha,Q15858,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1743,T3D0025,"DDD, P,P'-",Sodium channel protein type 1 subunit alpha,P35498,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1744,T3D0025,"DDD, P,P'-",Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1745,T3D0025,"DDD, P,P'-",Sodium channel protein type 11 subunit alpha,Q9UI33,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1746,T3D0025,"DDD, P,P'-",Sodium channel protein type 2 subunit alpha,Q99250,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1747,T3D0025,"DDD, P,P'-",Sodium channel protein type 3 subunit alpha,Q9NY46,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1748,T3D0025,"DDD, P,P'-",Sodium channel protein type 4 subunit alpha,P35499,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1749,T3D0025,"DDD, P,P'-",Sodium channel protein type 5 subunit alpha,Q14524,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1750,T3D0025,"DDD, P,P'-",Sodium channel protein type 7 subunit alpha,Q01118,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1751,T3D0025,"DDD, P,P'-",Sodium channel protein type 8 subunit alpha,Q9UQD0,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1752,T3D0025,"DDD, P,P'-",Sodium channel protein type 9 subunit alpha,Q15858,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1753,T3D0001,Arsenic,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1754,T3D0001,Arsenic,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1755,T3D0001,Arsenic,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
1759,T3D0006,Benzene,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,Direct binding of tubulin leads to protein damage. (R016)
1760,T3D0006,Benzene,Putative tubulin beta-4q chain,Q99867,Direct binding of tubulin leads to protein damage. (R016)
1761,T3D0006,Benzene,Putative tubulin-like protein alpha-4B,Q9H853,Direct binding of tubulin leads to protein damage. (R016)
1762,T3D0049,Cobalt,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1763,T3D0049,Cobalt,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
1764,T3D0049,Cobalt,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
1765,T3D0049,Cobalt,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
1766,T3D0049,Cobalt,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
1767,T3D0049,Cobalt,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
1768,T3D0049,Cobalt,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
1769,T3D0049,Cobalt,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
1770,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-1 subunit,Q06432,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1771,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-2 subunit,Q9Y698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1772,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-3 subunit,O60359,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1773,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-4 subunit,Q9UBN1,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1774,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-5 subunit,Q9UF02,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1775,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-6 subunit,Q9BXT2,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1776,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-7 subunit,P62955,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1777,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1778,T3D0049,Cobalt,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1779,T3D0049,Cobalt,Voltage-dependent calcium channel subunit alpha-2/delta-1,P54289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1780,T3D0049,Cobalt,"Calcium channel, alpha 2/delta subunit 2",Q9NY47,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1781,T3D0049,Cobalt,Voltage-dependent calcium channel subunit alpha-2/delta-3,Q8IZS8,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1782,T3D0049,Cobalt,Voltage-dependent calcium channel subunit alpha-2/delta-4,Q7Z3S7,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1783,T3D0049,Cobalt,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1784,T3D0049,Cobalt,Voltage-dependent L-type calcium channel subunit alpha-1F,O60840,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1785,T3D0049,Cobalt,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1786,T3D0049,Cobalt,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1787,T3D0049,Cobalt,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1788,T3D0049,Cobalt,Voltage-dependent L-type calcium channel subunit beta-3,P54284,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1789,T3D0049,Cobalt,Voltage-dependent L-type calcium channel subunit beta-4,O00305,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1790,T3D0049,Cobalt,Voltage-dependent N-type calcium channel subunit alpha-1B,Q00975,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1791,T3D0049,Cobalt,Voltage-dependent P/Q-type calcium channel subunit alpha-1A,O00555,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1792,T3D0049,Cobalt,Voltage-dependent R-type calcium channel subunit alpha-1E,Q15878,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
1793,T3D0053,Nickel,Histone H1.0,P07305,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1794,T3D0053,Nickel,Histone H1.1,Q02539,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1795,T3D0053,Nickel,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1796,T3D0053,Nickel,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1797,T3D0053,Nickel,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1798,T3D0053,Nickel,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1799,T3D0053,Nickel,Histone H1oo,Q8IZA3,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1800,T3D0053,Nickel,Histone H1t,P22492,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1801,T3D0053,Nickel,Histone H1x,Q92522,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1802,T3D0053,Nickel,Testis-specific H1 histone,Q75WM6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1803,T3D0053,Nickel,Histone H2A type 1,P0C0S8,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1804,T3D0053,Nickel,Histone H2A type 1-A,Q96QV6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1805,T3D0053,Nickel,Histone H2A type 1-B/E,P04908,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1806,T3D0053,Nickel,Histone H2A type 1-C,Q93077,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1807,T3D0053,Nickel,Histone H2A type 1-D,P20671,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1808,T3D0053,Nickel,Histone H2A type 1-H,Q96KK5,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1809,T3D0053,Nickel,Histone H2A type 1-J,Q99878,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1810,T3D0053,Nickel,Histone H2A type 2-A,Q6FI13,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1811,T3D0053,Nickel,Histone H2A type 2-B,Q8IUE6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1812,T3D0053,Nickel,Histone H2A type 2-C,Q16777,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1813,T3D0053,Nickel,Histone H2A type 3,Q7L7L0,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1814,T3D0053,Nickel,Histone H2A-Bbd type 1,P0C5Y9,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1815,T3D0053,Nickel,Histone H2A-Bbd type 2/3,P0C5Z0,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1816,T3D0053,Nickel,Histone H2A.J,Q9BTM1,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1817,T3D0053,Nickel,Histone H2A.V,Q71UI9,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1818,T3D0053,Nickel,Histone H2A.x,P16104,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1819,T3D0053,Nickel,Histone H2A.Z,P0C0S5,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1820,T3D0053,Nickel,Histone H2B type 1-A,Q96A08,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1821,T3D0053,Nickel,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1822,T3D0053,Nickel,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1823,T3D0053,Nickel,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1824,T3D0053,Nickel,Histone H2B type 1-H,Q93079,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1825,T3D0053,Nickel,Histone H2B type 1-J,P06899,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1826,T3D0053,Nickel,Histone H2B type 1-K,O60814,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1827,T3D0053,Nickel,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1828,T3D0053,Nickel,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1829,T3D0053,Nickel,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1830,T3D0053,Nickel,Histone H2B type 1-O,P23527,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1831,T3D0053,Nickel,Histone H2B type 2-E,Q16778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1832,T3D0053,Nickel,Histone H2B type 2-F,Q5QNW6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1833,T3D0053,Nickel,Histone H2B type 3-B,Q8N257,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1834,T3D0053,Nickel,Histone H2B type F-M,P0C1H6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1835,T3D0053,Nickel,Histone H2B type F-S,P57053,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1836,T3D0053,Nickel,Histone H2B type W-T,Q7Z2G1,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1837,T3D0053,Nickel,Histone H3-like,Q6NXT2,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1838,T3D0053,Nickel,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1839,T3D0053,Nickel,Histone H4-like protein type G,Q99525,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1840,T3D0053,Nickel,Putative histone H2B type 2-C ,Q6DN03	,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1841,T3D0053,Nickel,Putative histone H2B type 2-D,Q6DRA6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
1842,T3D0006,Benzene,Histone H1.0,P07305,Direct binding of histone leads to protein damage. (R016)
1843,T3D0006,Benzene,Histone H1.1,Q02539,Direct binding of histone leads to protein damage. (R016)
1844,T3D0006,Benzene,Histone H1.2,P16403,Direct binding of histone leads to protein damage. (R016)
1845,T3D0006,Benzene,Histone H1.3,P16402,Direct binding of histone leads to protein damage. (R016)
1846,T3D0006,Benzene,Histone H1.4,P10412,Direct binding of histone leads to protein damage. (R016)
1847,T3D0006,Benzene,Histone H1.5,P16401,Direct binding of histone leads to protein damage. (R016)
1848,T3D0006,Benzene,Histone H1oo,Q8IZA3,Direct binding of histone leads to protein damage. (R016)
1849,T3D0006,Benzene,Histone H1t,P22492,Direct binding of histone leads to protein damage. (R016)
1850,T3D0006,Benzene,Histone H1x,Q92522,Direct binding of histone leads to protein damage. (R016)
1851,T3D0006,Benzene,Histone H2A type 1,P0C0S8,Direct binding of histone leads to protein damage. (R016)
1852,T3D0006,Benzene,Histone H2A type 1-A,Q96QV6,Direct binding of histone leads to protein damage. (R016)
1853,T3D0006,Benzene,Histone H2A type 1-B/E,P04908,Direct binding of histone leads to protein damage. (R016)
1854,T3D0006,Benzene,Histone H2A type 1-C,Q93077,Direct binding of histone leads to protein damage. (R016)
1855,T3D0006,Benzene,Histone H2A type 1-D,P20671,Direct binding of histone leads to protein damage. (R016)
1856,T3D0006,Benzene,Histone H2A type 1-H,Q96KK5,Direct binding of histone leads to protein damage. (R016)
1857,T3D0006,Benzene,Histone H2A type 1-J,Q99878,Direct binding of histone leads to protein damage. (R016)
1858,T3D0006,Benzene,Histone H2B type 1-K,O60814,Direct binding of histone leads to protein damage. (R016)
1859,T3D0006,Benzene,Histone H2A type 2-A,Q6FI13,Direct binding of histone leads to protein damage. (R016)
1860,T3D0006,Benzene,Histone H2A type 2-B,Q8IUE6,Direct binding of histone leads to protein damage. (R016)
1861,T3D0006,Benzene,Histone H2A type 2-C,Q16777,Direct binding of histone leads to protein damage. (R016)
1862,T3D0006,Benzene,Histone H2A type 3,Q7L7L0,Direct binding of histone leads to protein damage. (R016)
1863,T3D0006,Benzene,Histone H2A-Bbd type 1,P0C5Y9,Direct binding of histone leads to protein damage. (R016)
1864,T3D0006,Benzene,Histone H2A-Bbd type 2/3,P0C5Z0,Direct binding of histone leads to protein damage. (R016)
1865,T3D0006,Benzene,Histone H2A.J,Q9BTM1,Direct binding of histone leads to protein damage. (R016)
1866,T3D0006,Benzene,Histone H2A.V,Q71UI9,Direct binding of histone leads to protein damage. (R016)
1867,T3D0006,Benzene,Histone H2A.x,P16104,Direct binding of histone leads to protein damage. (R016)
1868,T3D0006,Benzene,Histone H2A.Z,P0C0S5,Direct binding of histone leads to protein damage. (R016)
1869,T3D0006,Benzene,Histone H2B type 1-A,Q96A08,Direct binding of histone leads to protein damage. (R016)
1870,T3D0006,Benzene,Histone H2B type 1-B,P33778,Direct binding of histone leads to protein damage. (R016)
1871,T3D0006,Benzene,Histone H2B type 1-C/E/F/G/I,P62807,Direct binding of histone leads to protein damage. (R016)
1872,T3D0006,Benzene,Histone H2B type 1-D,P58876,Direct binding of histone leads to protein damage. (R016)
1873,T3D0006,Benzene,Histone H2B type 1-H,Q93079,Direct binding of histone leads to protein damage. (R016)
1874,T3D0006,Benzene,Histone H2B type 1-J,P06899,Direct binding of histone leads to protein damage. (R016)
1875,T3D0006,Benzene,Histone H2B type 1-L,Q99880,Direct binding of histone leads to protein damage. (R016)
1876,T3D0006,Benzene,Histone H2B type 1-M,Q99879,Direct binding of histone leads to protein damage. (R016)
1877,T3D0006,Benzene,Histone H2B type 1-N,Q99877,Direct binding of histone leads to protein damage. (R016)
1878,T3D0006,Benzene,Histone H2B type 1-O,P23527,Direct binding of histone leads to protein damage. (R016)
1879,T3D0006,Benzene,Histone H2B type 2-E,Q16778,Direct binding of histone leads to protein damage. (R016)
1880,T3D0006,Benzene,Histone H2B type 2-F,Q5QNW6,Direct binding of histone leads to protein damage. (R016)
1881,T3D0006,Benzene,Histone H2B type 3-B,Q8N257,Direct binding of histone leads to protein damage. (R016)
1882,T3D0006,Benzene,Histone H2B type F-M,P0C1H6,Direct binding of histone leads to protein damage. (R016)
1883,T3D0006,Benzene,Histone H2B type F-S,P57053,Direct binding of histone leads to protein damage. (R016)
1884,T3D0006,Benzene,Histone H2B type W-T,Q7Z2G1,Direct binding of histone leads to protein damage. (R016)
1885,T3D0006,Benzene,Histone H3-like,Q6NXT2,Direct binding of histone leads to protein damage. (R016)
1886,T3D0006,Benzene,Histone H3-like centromeric protein A,P49450,Direct binding of histone leads to protein damage. (R016)
1887,T3D0006,Benzene,Histone H4-like protein type G,Q99525,Direct binding of histone leads to protein damage. (R016)
1888,T3D0006,Benzene,Testis-specific H1 histone,Q75WM6,Direct binding of histone leads to protein damage. (R016)
1889,T3D0006,Benzene,Putative histone H2B type 2-C ,Q6DN03	,Direct binding of histone leads to protein damage. (R016)
1890,T3D0006,Benzene,Putative histone H2B type 2-D,Q6DRA6,Direct binding of histone leads to protein damage. (R016)
1891,T3D0050,"DDT, O,P'-",Sodium channel protein type 1 subunit alpha,P35498,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1892,T3D0050,"DDT, O,P'-",Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1893,T3D0050,"DDT, O,P'-",Sodium channel protein type 11 subunit alpha,Q9UI33,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1894,T3D0050,"DDT, O,P'-",Sodium channel protein type 2 subunit alpha,Q99250,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1895,T3D0050,"DDT, O,P'-",Sodium channel protein type 3 subunit alpha,Q9NY46,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1896,T3D0050,"DDT, O,P'-",Sodium channel protein type 4 subunit alpha,P35499,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1897,T3D0050,"DDT, O,P'-",Sodium channel protein type 5 subunit alpha,Q14524,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1898,T3D0050,"DDT, O,P'-",Sodium channel protein type 7 subunit alpha,Q01118,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1899,T3D0050,"DDT, O,P'-",Sodium channel protein type 8 subunit alpha,Q9UQD0,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1900,T3D0050,"DDT, O,P'-",Sodium channel protein type 9 subunit alpha,Q15858,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1901,T3D0050,"DDT, O,P'-",Sodium channel subunit beta-1,Q07699,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1902,T3D0050,"DDT, O,P'-",Sodium channel subunit beta-2,O60939,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1903,T3D0050,"DDT, O,P'-",Sodium channel subunit beta-3,Q9NY72,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1904,T3D0050,"DDT, O,P'-",Sodium channel subunit beta-4,Q8IWT1,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1905,T3D0012,"DDT, P,P'-",Sodium channel subunit beta-1,Q07699,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1906,T3D0012,"DDT, P,P'-",Sodium channel subunit beta-2,O60939,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1907,T3D0012,"DDT, P,P'-",Sodium channel subunit beta-3,Q9NY72,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1908,T3D0012,"DDT, P,P'-",Sodium channel subunit beta-4,Q8IWT1,"DDT inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1909,T3D0021,"DDE, P,P'-",Sodium channel subunit beta-1,Q07699,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1910,T3D0021,"DDE, P,P'-",Sodium channel subunit beta-2,O60939,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1911,T3D0021,"DDE, P,P'-",Sodium channel subunit beta-3,Q9NY72,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1912,T3D0021,"DDE, P,P'-",Sodium channel subunit beta-4,Q8IWT1,"DDE inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1913,T3D0025,"DDD, P,P'-",Sodium channel subunit beta-1,Q07699,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1914,T3D0025,"DDD, P,P'-",Sodium channel subunit beta-2,O60939,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1915,T3D0025,"DDD, P,P'-",Sodium channel subunit beta-3,Q9NY72,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1916,T3D0025,"DDD, P,P'-",Sodium channel subunit beta-4,Q8IWT1,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
1917,T3D0061,Methoxychlor,Sodium channel subunit beta-1,Q07699,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1918,T3D0061,Methoxychlor,Sodium channel subunit beta-2,O60939,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1919,T3D0061,Methoxychlor,Sodium channel subunit beta-3,Q9NY72,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1920,T3D0061,Methoxychlor,Sodium channel subunit beta-4,Q8IWT1,"As methoxychlor is also a structural analogue of DDT, it is believed to have the same neurotoxic effects. This includes preventing the deactivation of the sodium gate after neuron activation and membrane depolarization, resulting in hyperexcitability of the nerve. (R029, R323)"
1921,T3D0052,Di-n-butyl phthalate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Di-n-butyl phthalate has been shown to exhibit toxic effects in liver mitochondria by uncoupling energy-linked processes and inhibiting succinate dehydrogenase. (R259)
1922,T3D0052,Di-n-butyl phthalate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Di-n-butyl phthalate has been shown to exhibit toxic effects in liver mitochondria by uncoupling energy-linked processes and inhibiting succinate dehydrogenase. (R259)
1923,T3D0052,Di-n-butyl phthalate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Di-n-butyl phthalate has been shown to exhibit toxic effects in liver mitochondria by uncoupling energy-linked processes and inhibiting succinate dehydrogenase. (R259)
1924,T3D0052,Di-n-butyl phthalate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Di-n-butyl phthalate has been shown to exhibit toxic effects in liver mitochondria by uncoupling energy-linked processes and inhibiting succinate dehydrogenase. (R259)
1925,T3D0052,Di-n-butyl phthalate,Peroxisome proliferator-activated receptor alpha,Q07869,"Di-n-butyl phthalate causes peroxisome proliferation by activating peroxisome proliferator-activated receptors, which may lead to carcinogenic effects. (R262)"
1926,T3D0052,Di-n-butyl phthalate,Peroxisome proliferator-activated receptor gamma,P37231,"Di-n-butyl phthalate causes peroxisome proliferation by activating peroxisome proliferator-activated receptors, which may lead to carcinogenic effects. (R262)"
1928,T3D0770,Ethanol,Cytochrome P450 2E1,P05181,"Ethanol binds to the ubiquitination site of CYP2E1. Ethanol binds to the enzyme and blocks access to the ubiquitination site by the ubiquitin conjugating system. The ubiquitin binding site is at the substrate binding site of the CYP2E1 enzyme, thus preventing ubiquitin from binding at that site. (R267)"
1929,T3D0053,Nickel,Alpha-ketoglutarate-dependent dioxygenase alkB homolog 3,Q96Q83,"Nickel substitutes for iron in alpha-ketoglutarate-dependent dioxygenases, inhibiting DNA repair. (R295)"
1930,T3D0053,Nickel,JmjC domain-containing histone demethylation protein 3A,O75164,"Nickel substitutes for iron in jmjC domain-containing histone demethylation proteins, inhibiting their demethylation activity. (R295)"
1932,T3D0053,Nickel,Egl nine homolog 2,Q96KS0,"Nickel substitutes for iron in hypoxia-inducible factor prolyl hydroxylases, inhibiting their enzyme activity. This results in the accumulation of hypoxia inducible factor 1 alpha, causing hypoxia-mimic stress. (R295)"
1933,T3D0053,Nickel,JmjC domain-containing histone demethylation protein 2A,Q9Y4C1,"Nickel substitutes for iron in jmjC domain-containing histone demethylation proteins, inhibiting their demethylation activity. (R295)"
1934,T3D0053,Nickel,Egl nine homolog 1,Q9GZT9,"Nickel substitutes for iron in hypoxia-inducible factor prolyl hydroxylases, inhibiting their enzyme activity. This results in the accumulation of hypoxia inducible factor 1 alpha, causing hypoxia-mimic stress. (R295)"
1935,T3D0053,Nickel,Egl nine homolog 3,Q9H6Z9,"Nickel substitutes for iron in hypoxia-inducible factor prolyl hydroxylases, inhibiting their enzyme activity. This results in the accumulation of hypoxia inducible factor 1 alpha, causing hypoxia-mimic stress. (R295)"
1936,T3D0053,Nickel,Alpha-ketoglutarate-dependent dioxygenase alkB homolog 2,Q6NS38,"Nickel substitutes for iron in alpha-ketoglutarate-dependent dioxygenases, inhibiting DNA repair. (R295)"
1938,T3D0085,"1,2-Dichloroethane",Protein disulfide-isomerase,P07237,"S-(2-chloroethyl)glutathione, one of the glutathione conjugates of 1,2-dichloroethane, is known to irreversibly inhibit protein disulfide-isomerase via alkylation. (R374)"
1939,T3D0056,Diazinon,Acetylcholinesterase,P22303,"Diazoxon the main toxic intermediate of diazinon, inhibits acetylcholinesterase in the central and peripheral nervous system. This results in the accumulation of acetylcholine, causing excessive stimulation of cholinergic fibers in the postganglionic parasympathetic nerve endings, neuromuscular junctions of the skeletal muscles, and cells of the central nervous system that results in hyperpolarization and receptor desensitization. This produces muscarinic, nicotinic, and CNS effects. (R313)"
1940,T3D0056,Diazinon,Probable arylformamidase,Q63HM1,Diazoxon inhibits liver kynurenine formamidase. (R317)
1941,T3D0086,"2,4,6-Trichlorophenol",Acetylcholinesterase,P22303,"2,4,6-trichlorophenol (2,4,6-TCP) has been identified to hemolyze washed human erythrocytes and inhibit acetylcholinesterase (AchE) activities in the erythrocyte membrane. (R318)"
1942,T3D0058,Xylene,Cytochrome P450 2E1,P05181,Certain metabolites of xylene have been shown to inhibit pulmonary mixed-function oxidases. (R322)
1943,T3D0058,Xylene,Cytochrome P450 4B1,P13584,Certain metabolites of xylene have been shown to inhibit pulmonary mixed-function oxidases. (R322)
1944,T3D0059,"Chlordane, cis-","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Chlordane inhibit alkaline phosphatases in hepatic and renal tissues. (R206)
1947,T3D0059,"Chlordane, cis-",Cytochrome P450 2B6,P20813,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1948,T3D0059,"Chlordane, cis-",Cytochrome P450 3A4,P08684,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1949,T3D0059,"Chlordane, cis-",Cytochrome P450 3A43,Q9HB55,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1950,T3D0059,"Chlordane, cis-",Cytochrome P450 3A5,P20815,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1951,T3D0059,"Chlordane, cis-",Cytochrome P450 3A7,P24462,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
1952,T3D0059,"Chlordane, cis-",Estrogen-related receptor gamma,P62508,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162)
1954,T3D0059,"Chlordane, cis-",Retinoic acid receptor beta,P10826,"Chlordane has been shown to bind and activate retinoic acid receptor, causing various developmental defects. (R163)"
1955,T3D0059,"Chlordane, cis-",Retinoic acid receptor gamma-1,P13631,"Chlordane has been shown to bind and activate retinoic acid receptor, causing various developmental defects. (R163)"
1956,T3D0059,"Chlordane, cis-",Steroid hormone receptor ERR1,P11474,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162) 
1957,T3D0059,"Chlordane, cis-",Steroid hormone receptor ERR2,O95718,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162) 
1958,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial",P49821,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1959,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial",P19404,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1960,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] flavoprotein 3, mitochondrial",P56181,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1961,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial",O75306,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1962,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial",O75489,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1963,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial",O43181,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1964,T3D0060,Dibromochloropropane,NADH dehydrogenase [ubiquinone] iron-sulfur protein 5,O43920,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1965,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial",O75380,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1966,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial",O75251,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1967,T3D0060,Dibromochloropropane,"NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial",O00217,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1968,T3D0060,Dibromochloropropane,"NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial",P28331,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1970,T3D0060,Dibromochloropropane,NADH-ubiquinone oxidoreductase chain 2,P03891,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1971,T3D0060,Dibromochloropropane,NADH-ubiquinone oxidoreductase chain 3,P03897,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1972,T3D0060,Dibromochloropropane,NADH-ubiquinone oxidoreductase chain 4,P03905,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1973,T3D0060,Dibromochloropropane,NADH-ubiquinone oxidoreductase chain 4L,P03901,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1974,T3D0060,Dibromochloropropane,NADH-ubiquinone oxidoreductase chain 5,P03915,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1975,T3D0060,Dibromochloropropane,NADH-ubiquinone oxidoreductase chain 6,P03923,"Inhibition of sperm carbohydrate metabolism at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain is a factor of 1,2-dibromo-3-chloropropane's testicular toxicity. (R238)"
1976,T3D0061,Methoxychlor,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1977,T3D0061,Methoxychlor,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
1978,T3D0061,Methoxychlor,Androgen receptor,P10275,"Certain mono- and bis-hydroxy metabolites of methoxychlor, especially 2,2-bis(p-hydroxyphenyl)-1,1, 1-trichloroethane (HPTE), act as estrogen analogues. HPTE is an know androgen receptor antagonist. (R325)"
1979,T3D0063,Endrin ketone,Calcium-transporting ATPase type 2C member 1,P98194,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1980,T3D0069,Endrin aldehyde,Calcium-transporting ATPase type 2C member 1,P98194,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1981,T3D0063,Endrin ketone,Calcium-transporting ATPase type 2C member 2,O75185,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1982,T3D0069,Endrin aldehyde,Calcium-transporting ATPase type 2C member 2,O75185,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
1983,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1984,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1985,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1986,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1987,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1988,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1989,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1990,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1991,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1992,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1993,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1994,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1995,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1996,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1997,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1998,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
1999,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2000,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2001,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit delta,O14764,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2002,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit delta,O14764,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2003,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2004,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2005,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2006,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2007,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2008,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2009,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2010,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2011,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit pi,O00591,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2012,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit pi,O00591,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2013,T3D0063,Endrin ketone,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2014,T3D0069,Endrin aldehyde,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2015,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2016,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2017,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2018,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2019,T3D0063,Endrin ketone,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2020,T3D0069,Endrin aldehyde,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Endrin antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2021,T3D0063,Endrin ketone,Plasma membrane calcium-transporting ATPase 1,P20020,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2022,T3D0069,Endrin aldehyde,Plasma membrane calcium-transporting ATPase 1,P20020,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2023,T3D0063,Endrin ketone,Plasma membrane calcium-transporting ATPase 2,Q01814,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2024,T3D0069,Endrin aldehyde,Plasma membrane calcium-transporting ATPase 2,Q01814,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2025,T3D0063,Endrin ketone,Plasma membrane calcium-transporting ATPase 3,Q16720,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2026,T3D0069,Endrin aldehyde,Plasma membrane calcium-transporting ATPase 3,Q16720,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2027,T3D0063,Endrin ketone,Plasma membrane calcium-transporting ATPase 4,P23634,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2028,T3D0069,Endrin aldehyde,Plasma membrane calcium-transporting ATPase 4,P23634,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2029,T3D0063,Endrin ketone,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2030,T3D0069,Endrin aldehyde,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2031,T3D0063,Endrin ketone,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2032,T3D0069,Endrin aldehyde,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2033,T3D0063,Endrin ketone,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2034,T3D0069,Endrin aldehyde,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2035,T3D0063,Endrin ketone,Sodium/potassium-transporting ATPase gamma chain,P54710,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2036,T3D0069,Endrin aldehyde,Sodium/potassium-transporting ATPase gamma chain,P54710,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2037,T3D0063,Endrin ketone,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2038,T3D0069,Endrin aldehyde,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2039,T3D0063,Endrin ketone,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2040,T3D0069,Endrin aldehyde,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2041,T3D0063,Endrin ketone,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2042,T3D0069,Endrin aldehyde,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2043,T3D0063,Endrin ketone,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2044,T3D0069,Endrin aldehyde,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2045,T3D0063,Endrin ketone,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2046,T3D0069,Endrin aldehyde,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2047,T3D0063,Endrin ketone,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2048,T3D0069,Endrin aldehyde,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2049,T3D0063,Endrin ketone,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2050,T3D0069,Endrin aldehyde,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Endrin inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2051,T3D0064,"Chlordane, trans-","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Chlordane inhibit alkaline phosphatases in hepatic and renal tissues. (R206)
2053,T3D0064,"Chlordane, trans-",Cytochrome P450 2B6,P20813,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
2054,T3D0064,"Chlordane, trans-",Cytochrome P450 3A4,P08684,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
2055,T3D0064,"Chlordane, trans-",Cytochrome P450 3A43,Q9HB55,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
2056,T3D0064,"Chlordane, trans-",Cytochrome P450 3A5,P20815,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
2057,T3D0064,"Chlordane, trans-",Cytochrome P450 3A7,P24462,"Chlordane induces hepatic cytochrome P-450, causing a large increase in the volume of the smooth endoplasmic reticulum, which results in hepatocellular enlargement and hypertrophy. (R159, R205)"
2059,T3D0064,"Chlordane, trans-",Estrogen-related receptor gamma,P62508,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162)
2060,T3D0064,"Chlordane, trans-",Retinoic acid receptor beta,P10826,"Chlordane has been shown to bind and activate retinoic acid receptor, causing various developmental defects. (R163)"
2061,T3D0064,"Chlordane, trans-",Retinoic acid receptor gamma-1,P13631,"Chlordane has been shown to bind and activate retinoic acid receptor, causing various developmental defects. (R163)"
2062,T3D0064,"Chlordane, trans-",Steroid hormone receptor ERR1,P11474,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162) 
2063,T3D0064,"Chlordane, trans-",Steroid hormone receptor ERR2,O95718,Chlordane affects transcription by antagonizing estrogen-related receptors. (R162) 
2064,T3D0067,"Endosulfan, beta",Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Endosulfan antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions. (R194)"
2065,T3D0068,Aroclor 1232,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
2066,T3D0081,Aroclor 1240,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
2067,T3D0068,Aroclor 1232,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
2068,T3D0081,Aroclor 1240,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
2069,T3D0068,Aroclor 1232,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
2070,T3D0081,Aroclor 1240,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
2077,T3D0071,Toluene,Sodium channel protein type 5 subunit alpha,Q14524,"Toluene binds to cardiac Na+ channels in the open state and unbinds either when channels move between inactivated states or from an inactivated to a closed state. The use- and frequency-dependent block of Na+ by toluene might be responsible, at least in part, for its arrhythmogenic effect. (R201)"
2081,T3D0071,Toluene,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Toluene inhibits NMDA receptors, causing neurotoxic effects. (R340)"
2082,T3D0071,Toluene,Glutamate [NMDA] receptor subunit 3B,O60391,"Toluene inhibits NMDA receptors, causing neurotoxic effects. (R340)"
2083,T3D0071,Toluene,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Toluene inhibits NMDA receptors, causing neurotoxic effects. (R340)"
2084,T3D0071,Toluene,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Toluene inhibits NMDA receptors, causing neurotoxic effects. (R340)"
2085,T3D0071,Toluene,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Toluene inhibits NMDA receptors, causing neurotoxic effects. (R340)"
2086,T3D0071,Toluene,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Toluene inhibits NMDA receptors, causing neurotoxic effects. (R340)"
2087,T3D0071,Toluene,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Toluene inhibits NMDA receptors, causing neurotoxic effects. (R340)"
2088,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2089,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2090,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2091,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2092,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2093,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2094,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2095,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2096,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2097,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit delta,O14764,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2098,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2099,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2100,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2101,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2102,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit pi,O00591,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2103,T3D0071,Toluene,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2104,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2105,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2106,T3D0071,Toluene,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Toluene inhibits GABA(A) receptors, causing neurotoxic effects. (R338)"
2108,T3D0071,Toluene,Neuronal acetylcholine receptor subunit alpha-2,Q15822,"Toluene inhibits acetylcholine receptors, causing neurotoxic effects. (R341)"
2109,T3D0071,Toluene,Neuronal acetylcholine receptor subunit alpha-4,P43681,"Toluene inhibits acetylcholine receptors, causing neurotoxic effects. (R341)"
2110,T3D0071,Toluene,Neuronal acetylcholine receptor subunit alpha-5,P30532,"Toluene inhibits acetylcholine receptors, causing neurotoxic effects. (R341)"
2111,T3D0071,Toluene,Neuronal acetylcholine receptor subunit alpha-7,P36544,"Toluene inhibits acetylcholine receptors, causing neurotoxic effects. (R341)"
2112,T3D0071,Toluene,Neuronal acetylcholine receptor subunit beta-2,P17787,"Toluene inhibits acetylcholine receptors, causing neurotoxic effects. (R341)"
2113,T3D0071,Toluene,Neuronal acetylcholine receptor subunit alpha-9,Q9UGM1,"Toluene inhibits acetylcholine receptors, causing neurotoxic effects. (R341)"
2114,T3D0071,Toluene,Neuronal acetylcholine receptor subunit beta-4,P30926,"Toluene inhibits acetylcholine receptors, causing neurotoxic effects. (R341)"
2115,T3D0072,2-Hexanone,GTP:AMP phosphotransferase mitochondrial,Q9UIJ7,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as adenylate kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2116,T3D0072,2-Hexanone,Glyceraldehyde-3-phosphate dehydrogenase,P04406,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as glyceraldehyde-3-phosphate dehydrogenase , impairing energy metabolism and subsequently resulting in axon deterioration. (R344)"
2117,T3D0072,2-Hexanone,"Glyceraldehyde-3-phosphate dehydrogenase, testis-specific",O14556,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as glyceraldehyde-3-phosphate dehydrogenase , impairing energy metabolism and subsequently resulting in axon deterioration. (R344)"
2118,T3D0072,2-Hexanone,6-phosphofructokinase type C,Q01813,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as fructose-6-phosphate kinase, impairing energy metabolism and subsequently resulting in axon deterioration. (R344)"
2119,T3D0072,2-Hexanone,"6-phosphofructokinase, liver type",P17858,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as fructose-6-phosphate kinase, impairing energy metabolism and subsequently resulting in axon deterioration. (R344)"
2120,T3D0072,2-Hexanone,"6-phosphofructokinase, muscle type",P08237,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as fructose-6-phosphate kinase, impairing energy metabolism and subsequently resulting in axon deterioration. (R344)"
2121,T3D0072,2-Hexanone,Creatine kinase B-type,P12277,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as creatine kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2122,T3D0072,2-Hexanone,"Creatine kinase, sarcomeric mitochondrial",P17540,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as creatine kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2123,T3D0072,2-Hexanone,Creatine kinase M-type,P06732,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as creatine kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2124,T3D0072,2-Hexanone,"Creatine kinase, ubiquitous mitochondrial",P12532,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as creatine kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2125,T3D0072,2-Hexanone,"Adenylate kinase isoenzyme 2, mitochondrial",P54819,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as adenylate kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2126,T3D0072,2-Hexanone,Adenylate kinase isoenzyme 1,P00568,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as adenylate kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2127,T3D0072,2-Hexanone,"Adenylate kinase isoenzyme 4, mitochondrial",P27144,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as adenylate kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2128,T3D0072,2-Hexanone,Adenylate kinase isoenzyme 5,Q9Y6K8,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as adenylate kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2129,T3D0072,2-Hexanone,Adenylate kinase isoenzyme 6,Q9Y3D8,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as adenylate kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2130,T3D0072,2-Hexanone,Putative adenylate kinase 7,Q96M32,"2-Hexanone and 2,5-hexanedione may inhibit sulfhydryl-dependent enzymes such as adenylate kinases, impairing energy metabolism and subsequently resulting in axon deterioration. (R345)"
2131,T3D0087,"2,4-Dinitrophenol",Transthyretin,P02766,"2,4-Dinitrophenol has been suggested to bind serum proteins such as transthyretin. In fact it was proposed as a therapeutic agent for the prevention/inhibition of amyloid diseases through stabilization of the native fold of transthyretin. (R348,R349)"
2132,T3D0073,"2,3,7,8-Tetrachlorodibenzo-p-dioxin",Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2133,T3D0204,Pentachlorodibenzo-p-dioxin,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2135,T3D0153,Hexachlorodibenzo-p-dioxin,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2136,T3D0154,Heptachlorodibenzo-p-dioxin,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2137,T3D0202,Tetrachlorodibenzo-p-dioxin,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2139,T3D0075,Dimethylarsinic acid,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
2140,T3D0075,Dimethylarsinic acid,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
2141,T3D0075,Dimethylarsinic acid,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
2142,T3D0075,Dimethylarsinic acid,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
2143,T3D0075,Dimethylarsinic acid,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
2144,T3D0075,Dimethylarsinic acid,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
2145,T3D0075,Dimethylarsinic acid,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
2146,T3D0075,Dimethylarsinic acid,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
2147,T3D0075,Dimethylarsinic acid,Estrogen receptor,P03372,"Arsenic binds to the estrogen receptor. (R054)
"
2148,T3D0075,Dimethylarsinic acid,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054
2149,T3D0075,Dimethylarsinic acid,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
2150,T3D0075,Dimethylarsinic acid,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
2151,T3D0075,Dimethylarsinic acid,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
2152,T3D0075,Dimethylarsinic acid,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
2153,T3D0075,Dimethylarsinic acid,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2154,T3D0075,Dimethylarsinic acid,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2155,T3D0075,Dimethylarsinic acid,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2156,T3D0075,Dimethylarsinic acid,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
2157,T3D0075,Dimethylarsinic acid,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
2158,T3D0075,Dimethylarsinic acid,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
2160,T3D0075,Dimethylarsinic acid,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
2161,T3D0075,Dimethylarsinic acid,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
2162,T3D0075,Dimethylarsinic acid,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
2163,T3D0075,Dimethylarsinic acid,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
2164,T3D0075,Dimethylarsinic acid,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2165,T3D0075,Dimethylarsinic acid,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2166,T3D0075,Dimethylarsinic acid,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2167,T3D0075,Dimethylarsinic acid,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2168,T3D0075,Dimethylarsinic acid,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2169,T3D0075,Dimethylarsinic acid,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2170,T3D0075,Dimethylarsinic acid,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2171,T3D0075,Dimethylarsinic acid,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2172,T3D0075,Dimethylarsinic acid,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2173,T3D0075,Dimethylarsinic acid,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2174,T3D0075,Dimethylarsinic acid,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2175,T3D0075,Dimethylarsinic acid,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2176,T3D0075,Dimethylarsinic acid,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2177,T3D0075,Dimethylarsinic acid,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2178,T3D0075,Dimethylarsinic acid,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2179,T3D0075,Dimethylarsinic acid,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2180,T3D0075,Dimethylarsinic acid,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2181,T3D0075,Dimethylarsinic acid,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2182,T3D0075,Dimethylarsinic acid,Tubulin delta chain,Q9UJT1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2183,T3D0075,Dimethylarsinic acid,Tubulin epsilon chain,Q9UJT0,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2184,T3D0075,Dimethylarsinic acid,Tubulin gamma-1 chain,P23258,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2185,T3D0075,Dimethylarsinic acid,Tubulin gamma-2 chain,Q9NRH3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
2186,T3D0076,Di(2-ethylhexyl)phthalate,Peroxisome proliferator-activated receptor alpha,Q07869,"Monoethylhexylphthalate (MEHP), one of the major metabolites of DEHP, induces peroxisome proliferation by activating peroxisome proliferator activated receptors. This is believed to increase production of hydrogen peroxide by peroxisomes and enhance cell proliferation, leading to hepatotoxic and carcinogenic effects. (R359)"
2187,T3D0076,Di(2-ethylhexyl)phthalate,Peroxisome proliferator-activated receptor delta,Q03181,"Monoethylhexylphthalate (MEHP), one of the major metabolites of DEHP, induces peroxisome proliferation by activating peroxisome proliferator activated receptors. This is believed to increase production of hydrogen peroxide by peroxisomes and enhance cell proliferation, leading to hepatotoxic and carcinogenic effects. (R359)"
2188,T3D0076,Di(2-ethylhexyl)phthalate,Peroxisome proliferator-activated receptor gamma,P37231,"Monoethylhexylphthalate (MEHP), one of the major metabolites of DEHP, induces peroxisome proliferation by activating peroxisome proliferator activated receptors. This is believed to increase production of hydrogen peroxide by peroxisomes and enhance cell proliferation, leading to hepatotoxic and carcinogenic effects. (R359)"
2189,T3D0771,Methanol,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2190,T3D0771,Methanol,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2192,T3D0771,Methanol,Cytochrome c oxidase subunit 1,P00395,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2193,T3D0771,Methanol,Cytochrome c oxidase subunit 2,P00403,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2194,T3D0771,Methanol,Cytochrome c oxidase subunit 3,P00414,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2195,T3D0771,Methanol,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2196,T3D0771,Methanol,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2197,T3D0771,Methanol,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2198,T3D0771,Methanol,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2199,T3D0771,Methanol,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2200,T3D0771,Methanol,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2201,T3D0771,Methanol,Cytochrome c oxidase subunit 6B1,P14854,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2202,T3D0771,Methanol,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2204,T3D0771,Methanol,Cytochrome c oxidase subunit 6C,P09669,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2205,T3D0771,Methanol,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2206,T3D0771,Methanol,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2207,T3D0080,Methylene chloride,Hemoglobin subunit alpha,P69905,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2208,T3D0771,Methanol,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2209,T3D0771,Methanol,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2210,T3D0771,Methanol,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2211,T3D0771,Methanol,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"The toxic metabolite of Methanol that responsible for the retinal and optic nerve toxicity produced in methanol intoxication is Formic acid. Formic acid is a mitochondrial toxin that inhibits cytochrome c oxidase, the terminal enzyme of the mitochondrial electron transport chain of all eukaryotes. (R369)"
2212,T3D0080,Methylene chloride,Hemoglobin subunit beta,P68871,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2213,T3D0080,Methylene chloride,Hemoglobin subunit delta,P02042,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2214,T3D0080,Methylene chloride,Hemoglobin subunit epsilon,P02100,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2215,T3D0080,Methylene chloride,Hemoglobin subunit gamma-1,P69891,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2216,T3D0080,Methylene chloride,Hemoglobin subunit gamma-2,P69892,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2217,T3D0080,Methylene chloride,Hemoglobin subunit mu,Q6B0K9,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2218,T3D0080,Methylene chloride,Hemoglobin subunit theta-1,P09105,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2219,T3D0080,Methylene chloride,Hemoglobin subunit zeta,P02008,"Methylene chloride is metabolized into carbon monoxide, which binds to hemoglobin to produce dose-dependent increases in carboxyhemoglobin. This results in the reduced oxygen transport and neurological dysfunction characteristic of carboxyhemoglobinemia (carbon monoxide poisoning). (R366)"
2221,T3D0115,"Hexachlorocyclohexane, alpha-",Gamma-aminobutyric acid receptor subunit epsilon,P78334,"This organochloride antagonizes the action of the neurotransmitter gamma-aminobutyric acid (GABA) acting at the GABA-A receptors, effectively blocking the GABA-induced uptake of chloride ions and causing hyperexcitability of the central nervous system. (R029)"
2222,T3D0102,"4,6-Dinitro-o-cresol","Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,"4,6-Dinitro-o-cresol decreases mitochondrial respiration by inhibiting the
activity of succinate dehydrogenase, preventing succinate oxidation. (R381)"
2223,T3D0102,"4,6-Dinitro-o-cresol","Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,"4,6-Dinitro-o-cresol decreases mitochondrial respiration by inhibiting the
activity of succinate dehydrogenase, preventing succinate oxidation. (R381)"
2224,T3D0102,"4,6-Dinitro-o-cresol","Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,"4,6-Dinitro-o-cresol decreases mitochondrial respiration by inhibiting the
activity of succinate dehydrogenase, preventing succinate oxidation. (R381)"
2225,T3D0102,"4,6-Dinitro-o-cresol","Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,"4,6-Dinitro-o-cresol decreases mitochondrial respiration by inhibiting the
activity of succinate dehydrogenase, preventing succinate oxidation. (R381)"
2226,T3D0783,Glyphosate,Basic salivary proline-rich protein 1,P04280,"The CP4 enzyme has unexpected kinetic and structural properties that render it unique among the known EPSP synthases. Glyphosate binds to the CP4 EPSP synthase in a condensed, noninhibitory conformation. (R384)"
2227,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit alpha,P69905,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2228,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit beta,P68871,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2229,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit delta,P02042,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2230,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit epsilon,P02100,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2231,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit gamma-1,P69891,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2232,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit gamma-2,P69892,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2233,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit mu,Q6B0K9,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2234,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit theta-1,P09105,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2235,T3D0782,"1,3-Dinitrobenzene",Hemoglobin subunit zeta,P02008,"Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and methemoglobin. This elevation of methemoglobin levels is a condition known as methemoglobinemia, and is characterized by tissue hypoxia, as methemoglobin cannot bind oxygen. (V305, V306)"
2236,T3D0089,Thiocyanate,Lactoperoxidase,P22079,"The LPO enzyme catalyzes the peroxidation of thiocyanate in the presence of H2O2. In order for the reaction to occur, the SCN– ion must bind to LPO at the substrate-binding site in the distal heme cavity with a favorable orientation. (R387)"
2237,T3D0089,Thiocyanate,Myeloperoxidase,P05164,Myeloperoxidase is considered to oxidize thiocyanate to hypothiocyanite either directly or via initial formation of thiocyanogen which rapidly hydrolyses to hypothiocyanite. (R388)
2238,T3D0089,Thiocyanate,Eosinophil peroxidase,P11678,"Thiocyanate is known to modulate activity of mammalian peroxidases, such as eosinophil peroxidase has been implicated in promoting oxidative tissue damage in a variety of in ammatory conditions, including asthma. It uses H2O2 to oxidize chloride, bromide and thiocyanate to their respective hypohalous acids. (R389)"
2239,T3D0089,Thiocyanate,Sodium/iodide cotransporter,Q92911,"Thiocyanate is a competitive inhibitor of the human thyroid sodium/iodide symporter NIS, which plays an important role in moving thiocyanate ions into epithelial cells. (R390, R410)"
2240,T3D0109,Barium,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
2241,T3D0089,Thiocyanate,Carbonic anhydrase 2,P00918,"Thiocyanates also act as inhibitors to carbonic anhydrase, which catalyzes the rapid conversion of carbon dioxide to bicarbonate and protons. (R417)"
2242,T3D0089,Thiocyanate,Carbonic anhydrase 4,P22748,"Thiocyanates also act as inhibitors to carbonic anhydrase, which catalyzes the rapid conversion of carbon dioxide to bicarbonate and protons. (R417)"
2244,T3D0089,Thiocyanate,Carbonic anhydrase 3,P07451,"Thiocyanates also act as inhibitors to carbonic anhydrase, which catalyzes the rapid conversion of carbon dioxide to bicarbonate and protons. (R417)"
2245,T3D0089,Thiocyanate,Carbonic anhydrase 1,P00915,"Thiocyanates also act as inhibitors to carbonic anhydrase, which catalyzes the rapid conversion of carbon dioxide to bicarbonate and protons. (R417)"
2246,T3D0109,Barium,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2247,T3D0109,Barium,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2248,T3D0109,Barium,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2249,T3D0109,Barium,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2250,T3D0109,Barium,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2251,T3D0109,Barium,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2252,T3D0109,Barium,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2253,T3D0109,Barium,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2254,T3D0109,Barium,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2255,T3D0109,Barium,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2256,T3D0109,Barium,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2257,T3D0109,Barium,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2258,T3D0109,Barium,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2260,T3D0109,Barium,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2261,T3D0109,Barium,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
2262,T3D0109,Barium,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
2263,T3D0109,Barium,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
2264,T3D0109,Barium,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
2265,T3D0109,Barium,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
2266,T3D0109,Barium,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
2267,T3D0112,n-Nitrosodi-n-propylamine,DNA,DNA,"Reactive metabolites of n-nitrosodi-n-propylamine are believed to form adducts with DNA, resulting in carcinogenic effects. (R420)"
2268,T3D0004,Vinyl chloride,DNA,DNA,"The metabolites of vinyl chloride, especially choloroethylene oxide, are mutagenic and act by covalently binding to DNA. This produces cyclic etheno-adducts, which cause base-pair transitions during transcription and DNA crosslinks. (R010)"
2269,T3D0006,Benzene,DNA,DNA,"Benzene may covalently binding to DNA, causing effects such as strand breakage, mitotic recombination, chromosome translocations, and aneuploidy. (R016)"
2271,T3D0009,Benzo[a]pyrene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2272,T3D0010,Benzo[b]fluoranthene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2273,T3D0015,"Dibenzo[a,h]anthracene",DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2274,T3D0018,"Chromium, hexavalent",DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
2275,T3D0020,Chlordane,DNA,DNA,"Chlordane is believed to bind irreversibly to DNA, leading to cell death or altered cellular function. (R159)"
2276,T3D0039,Benzo[a]anthracene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2277,T3D0022,Hexachlorobutadiene,DNA,DNA,The carcinogenic properties of hexachlorobutadiene are proposed to result from binding of the sulfenic acid degradation product or a thioketene intermediate to cellular DNA. (R166)
2278,T3D0026,Benzidine,DNA,DNA,"N-acetylated benzidine metabolites are believed to form adducts with nucleic acids. Carcinogenesis is initiated when they are activated by peroxidation by prostaglandin H synthetase, oxidation by cytochrome P-450, or O-esterification by O-acetyltransferase or N,O-acetyltransferase. (R168)"
2279,T3D0035,"1,2-Dibromoethane",DNA,DNA,"S-(2-bromoethyl)glutathione, a metabolite of 1,2-dibromoethane, exerts genotoxic and carcinogenic effects by binding to DNA. (R222)"
2280,T3D0040,"3,3'-Dichlorobenzidine",DNA,DNA,"3,3’-Dichlorobenzidine`s mechanism of toxicity derivies mainly from the adduction of DNA by its metabolites. The formation of nitroso derivatives during metabolism, yielding a sulfinic acid amide with hemoglobin in erythrocytes, is suggested to be a mechanism for this adduct formation. (R232, R233)"
2281,T3D0044,"1,2-Dibromo-3-chloropropane",DNA,DNA,"The initial metabolism of 1,2-dibromo-3-chloropropane to reactive epoxide metabolites that bind to DNA and other macromolecules may be responsible for its hepatotoxicity and nephrotoxicity. The mechanism of 1,2-dibromo-3-chloropropane's testicular toxicity is believed to be due to either the inhibition of sperm carbohydrate metabolism, probably at the step of nicotinamide adenine dinucleotide (NADH) dehydrogenase activity in the mitochondrial electron transport chain, or drect DNA damage caused by its metabolites. (R236, R238)"
2282,T3D0047,Carbon tetrachloride,DNA,DNA,"Carbon tetrachloride's carcinogenicity is likely the result of certain reactive metabolites that bind to nuclear proteins, lipids, and DNA. (R245)"
2283,T3D0049,Cobalt,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
2284,T3D0062,Benzo[k]fluoranthene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2285,T3D0070,Benzofluoranthene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2286,T3D0077,Chromium,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
2287,T3D0065,Chromium(VI) oxide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
2288,T3D0078,Naphthalene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2289,T3D0064,"Chlordane, trans-",DNA,DNA,"Chlordane is believed to bind irreversibly to DNA, leading to cell death or altered cellular function. (R159)"
2290,T3D0110,Fluoranthene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2291,T3D0059,"Chlordane, cis-",DNA,DNA,"Chlordane is believed to bind irreversibly to DNA, leading to cell death or altered cellular function. (R159)"
2292,T3D0093,Hexachlorobenzene,Aryl hydrocarbon receptor,P35869,"Hexachlorobenzene is a weak agonist for aryl hydrocarbon receptor and may exhibit some of its toxic effects by activating the gene-regulatory properties of this protein, possibly inducing cytochome P-450 enzymes. (R439)"
2293,T3D0093,Hexachlorobenzene,Estrogen-related receptor gamma,P62508,Hexachlorobenzene is an antagonist for the estrogen-related receptor gamma. (R440)
2294,T3D0093,Hexachlorobenzene,Androgen receptor,P10275,Hexachlorobenzene is an antagonist for the androgren receptor. (R440)
2295,T3D0093,Hexachlorobenzene,DNA,DNA,"Metabolism of hexachlorobenzene by the cytochrome P-450 enzymes is believed to produce reactive electrophilic metabolites that covalently bind to cellular proteins and DNA, causing irreversible damage. (R435)"
2296,T3D0090,Asbestos,DNA,DNA,"Asbestos fibers bind to DNA. The coulombic forces between the asbestos fiber and DNA may induce conformational changes, and these changes could affect chromosomal fidelity. (R427)"
2297,T3D0117,Manganese,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
2298,T3D0117,Manganese,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
2299,T3D0117,Manganese,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
2300,T3D0117,Manganese,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
2301,T3D0117,Manganese,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
2303,T3D0179,Uranium-233,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466) "
2304,T3D0111,Uranium-234,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466) "
2305,T3D0108,Uranium-235,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466) "
2306,T3D0791,Uranium-238,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466) "
2307,T3D0123,Methylmercury,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2308,T3D0123,Methylmercury,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
2309,T3D0123,Methylmercury,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
2310,T3D0123,Methylmercury,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2311,T3D0123,Methylmercury,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2312,T3D0123,Methylmercury,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2313,T3D0123,Methylmercury,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2314,T3D0123,Methylmercury,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2315,T3D0123,Methylmercury,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2316,T3D0123,Methylmercury,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2317,T3D0123,Methylmercury,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2318,T3D0123,Methylmercury,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2319,T3D0123,Methylmercury,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2320,T3D0123,Methylmercury,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2321,T3D0123,Methylmercury,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2322,T3D0123,Methylmercury,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2323,T3D0123,Methylmercury,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2324,T3D0361,Dimethyl mercury,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2325,T3D0361,Dimethyl mercury,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
2326,T3D0361,Dimethyl mercury,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
2327,T3D0361,Dimethyl mercury,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2328,T3D0361,Dimethyl mercury,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2329,T3D0361,Dimethyl mercury,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2330,T3D0361,Dimethyl mercury,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2331,T3D0361,Dimethyl mercury,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2332,T3D0361,Dimethyl mercury,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2333,T3D0361,Dimethyl mercury,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2334,T3D0361,Dimethyl mercury,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2335,T3D0361,Dimethyl mercury,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
2336,T3D0361,Dimethyl mercury,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2337,T3D0361,Dimethyl mercury,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2338,T3D0361,Dimethyl mercury,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2339,T3D0361,Dimethyl mercury,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2340,T3D0361,Dimethyl mercury,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
2341,T3D0127,Chlorpyrifos,Acetylcholinesterase,P22303,"Chlorpyrifos and its bioactivation product, chlorpyrifos oxon, and inhibit neural acetylcholinesterase by forming a stable covalent bond at the active site. The result of this acetylcholinesterase inhibition is cholinergic overstimulation of the central nervous system. (R488)"
2342,T3D0127,Chlorpyrifos,Muscarinic acetylcholine receptor M1,P11229,"Chlorpyrifos oxon binds to muscarinic receptors, altering the receptors signal transduction, which affects cellular signalling and disrupts neurological function. (R495)"
2343,T3D0127,Chlorpyrifos,Muscarinic acetylcholine receptor M2,P08172,"Chlorpyrifos oxon binds to muscarinic receptors, altering the receptors signal transduction, which affects cellular signalling and disrupts neurological function. (R495)"
2344,T3D0127,Chlorpyrifos,Muscarinic acetylcholine receptor M3,P20309,"Chlorpyrifos oxon binds to muscarinic receptors, altering the receptors signal transduction, which affects cellular signalling and disrupts neurological function. (R495)"
2345,T3D0127,Chlorpyrifos,Muscarinic acetylcholine receptor M4,P08173,"Chlorpyrifos oxon binds to muscarinic receptors, altering the receptors signal transduction, which affects cellular signalling and disrupts neurological function. (R495)"
2346,T3D0127,Chlorpyrifos,Muscarinic acetylcholine receptor M5,P08912,"Chlorpyrifos oxon binds to muscarinic receptors, altering the receptors signal transduction, which affects cellular signalling and disrupts neurological function. (R495)"
2347,T3D0127,Chlorpyrifos,Serum albumin,P02768,Chlorpyrifos oxon binds albumin and may generate an antibody response. (R496)
2348,T3D0127,Chlorpyrifos,Cytochrome P450 3A4,P08684,Chlorpyrifos is an irreversible non-competitive inhibitor of cytochrome P-450 3A4. (R498)
2349,T3D0127,Chlorpyrifos,Neuropathy target esterase,Q8IY17,"Chlorpyrifos inhibits neuropathy target esterase, producing ataxia. (R499)"
2350,T3D0127,Chlorpyrifos,Cannabinoid receptor 1,P21554,Chlorpyrifos oxon inhibits cannabinoid receptor 1. (R500)
2351,T3D0131,Amosite asbestos,DNA,DNA,"Asbestos fibers bind to DNA. The coulombic forces between the asbestos fiber and DNA may induce conformational changes, and these changes could affect chromosomal fidelity. (R427)"
2352,T3D0119,Chrysotile asbestos,DNA,DNA,"Asbestos fibers bind to DNA. The coulombic forces between the asbestos fiber and DNA may induce conformational changes, and these changes could affect chromosomal fidelity. (R427)"
2353,T3D0792,Crocidolite Asbestos,DNA,DNA,"Asbestos fibers bind to DNA. The coulombic forces between the asbestos fiber and DNA may induce conformational changes, and these changes could affect chromosomal fidelity. (R427)"
2354,T3D0793,Tremolite Asbestos,DNA,DNA,"Asbestos fibers bind to DNA. The coulombic forces between the asbestos fiber and DNA may induce conformational changes, and these changes could affect chromosomal fidelity. (R427)"
2355,T3D0794,Actinolite Asbestos,DNA,DNA,"Asbestos fibers bind to DNA. The coulombic forces between the asbestos fiber and DNA may induce conformational changes, and these changes could affect chromosomal fidelity. (R427)"
2356,T3D0795,Anthophyllite Asbestos,DNA,DNA,"Asbestos fibers bind to DNA. The coulombic forces between the asbestos fiber and DNA may induce conformational changes, and these changes could affect chromosomal fidelity. (R427)"
2357,T3D0094,"2,4-Dinitrotoluene",DNA,DNA,"2,4-DNT and its metabolites may covalently bind to DNA. (R517, R518)"
2358,T3D0094,"2,4-Dinitrotoluene",RNA,RNA,"2,4-DNT and its metabolites may covalently bind to RNA. (R519)"
2359,T3D0128,Copper,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
2362,T3D0128,Copper,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of β-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
2363,T3D0128,Copper,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
2364,T3D0128,Copper,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
2365,T3D0128,Copper,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
2366,T3D0128,Copper,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
2370,T3D0133,Hydrogen cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
2371,T3D0133,Hydrogen cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
2372,T3D0133,Hydrogen cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
2373,T3D0133,Hydrogen cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
2374,T3D0133,Hydrogen cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212) 
2375,T3D0133,Hydrogen cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
2376,T3D0133,Hydrogen cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213) 
2377,T3D0133,Hydrogen cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213) 
2378,T3D0133,Hydrogen cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213) 
2379,T3D0133,Hydrogen cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213) 
2380,T3D0097,"1,1,1-Trichloroethane",Acetylcholinesterase,P22303,"1,1,1-Trichloroethane inhibits the activity of membrane-bound enzymes such as acetylcholinesterase. (R564)"
2381,T3D0097,"1,1,1-Trichloroethane",DNA,DNA,"1,1,1-Trichloroethane binds covalently to DNA. (R565, R566)"
2382,T3D0097,"1,1,1-Trichloroethane",RNA,RNA,"1,1,1-Trichloroethane binds covalently to RNA. (R566)"
2383,T3D0134,Tributyltin,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
2384,T3D0796,Tin,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
2385,T3D0134,Tributyltin,Alcohol dehydrogenase 1A,P07327,Organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2386,T3D0134,Tributyltin,Alcohol dehydrogenase 1B,P00325,Organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2387,T3D0134,Tributyltin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2388,T3D0134,Tributyltin,Alcohol dehydrogenase 4,P08319,Organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2389,T3D0134,Tributyltin,Alcohol dehydrogenase 6,P28332,Organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2390,T3D0134,Tributyltin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2391,T3D0134,Tributyltin,Alcohol dehydrogenase class-3,P11766,Organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2392,T3D0796,Tin,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2393,T3D0796,Tin,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2394,T3D0796,Tin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2395,T3D0796,Tin,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2396,T3D0796,Tin,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2397,T3D0796,Tin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2398,T3D0796,Tin,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
2399,T3D0796,Tin,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571) "
2400,T3D0796,Tin,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571) "
2401,T3D0796,Tin,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571) "
2402,T3D0796,Tin,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571) "
2403,T3D0134,Tributyltin,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571) "
2404,T3D0134,Tributyltin,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571) "
2405,T3D0134,Tributyltin,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571) "
2406,T3D0134,Tributyltin,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571) "
2407,T3D0796,Tin,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
2408,T3D0796,Tin,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
2409,T3D0796,Tin,Thioredoxin reductase 3,Q86VQ6,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
2410,T3D0134,Tributyltin,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
2411,T3D0134,Tributyltin,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
2412,T3D0134,Tributyltin,Thioredoxin reductase 3,Q86VQ6,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
2413,T3D0797,Imidacloprid,Acetylcholine receptor subunit alpha,P02708,Imidacloprid binds specifically to nicotinic acetylcholine receptors in various nervous systems and acts as a partial agonist. (R029)
2414,T3D0797,Imidacloprid,Acetylcholine receptor subunit beta,P11230,Imidacloprid binds specifically to nicotinic acetylcholine receptors in various nervous systems and acts as a partial agonist. (R029)
2415,T3D0797,Imidacloprid,Acetylcholine receptor subunit delta,Q07001,Imidacloprid binds specifically to nicotinic acetylcholine receptors in various nervous systems and acts as a partial agonist. (R029)
2416,T3D0797,Imidacloprid,Acetylcholine receptor subunit epsilon,Q04844,Imidacloprid binds specifically to nicotinic acetylcholine receptors in various nervous systems and acts as a partial agonist. (R029)
2417,T3D0797,Imidacloprid,Acetylcholine receptor subunit gamma,P07510,Imidacloprid binds specifically to nicotinic acetylcholine receptors in various nervous systems and acts as a partial agonist. (R029)
2418,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2419,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2420,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2421,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2422,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2423,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2424,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2425,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2426,T3D0798,Fipronil,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2427,T3D0798,Fipronil,Gamma-aminobutyric acid receptor subunit delta,O14764,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2428,T3D0798,Fipronil,Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2429,T3D0798,Fipronil,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2430,T3D0798,Fipronil,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2431,T3D0798,Fipronil,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2432,T3D0798,Fipronil,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,"Fipronil blocks the passage of chloride ions through the GABA-regulated chloride channel, disrupting CNS activity. (R029)"
2435,T3D0799,Nicotine,Acetylcholine receptor subunit alpha,P02708,"Nicotine binds to the nicotinic acetylcholine receptor. Stimulation of nicotinic receptors leads to a variety of cholinergic and adrenergic effects; tachycardia or bradycardia mediated by either stimulation or interference with sympathetic or parasympathetic pathways, stimulation of receptors in the carotic and aortic bodies, release of epinephrine from the adrenal medulla, and stimulation of the chemoreceptor-trigger zone. (S480)"
2436,T3D0799,Nicotine,Acetylcholine receptor subunit beta,P11230,"Nicotine binds to the nicotinic acetylcholine receptor. Stimulation of nicotinic receptors leads to a variety of cholinergic and adrenergic effects; tachycardia or bradycardia mediated by either stimulation or interference with sympathetic or parasympathetic pathways, stimulation of receptors in the carotic and aortic bodies, release of epinephrine from the adrenal medulla, and stimulation of the chemoreceptor-trigger zone. (S480)"
2437,T3D0799,Nicotine,Acetylcholine receptor subunit delta,Q07001,"Nicotine binds to the nicotinic acetylcholine receptor. Stimulation of nicotinic receptors leads to a variety of cholinergic and adrenergic effects; tachycardia or bradycardia mediated by either stimulation or interference with sympathetic or parasympathetic pathways, stimulation of receptors in the carotic and aortic bodies, release of epinephrine from the adrenal medulla, and stimulation of the chemoreceptor-trigger zone. (S480)"
2438,T3D0799,Nicotine,Acetylcholine receptor subunit epsilon,Q04844,"Nicotine binds to the nicotinic acetylcholine receptor. Stimulation of nicotinic receptors leads to a variety of cholinergic and adrenergic effects; tachycardia or bradycardia mediated by either stimulation or interference with sympathetic or parasympathetic pathways, stimulation of receptors in the carotic and aortic bodies, release of epinephrine from the adrenal medulla, and stimulation of the chemoreceptor-trigger zone. (S480)"
2439,T3D0799,Nicotine,Acetylcholine receptor subunit gamma,P07510,"Nicotine binds to the nicotinic acetylcholine receptor. Stimulation of nicotinic receptors leads to a variety of cholinergic and adrenergic effects; tachycardia or bradycardia mediated by either stimulation or interference with sympathetic or parasympathetic pathways, stimulation of receptors in the carotic and aortic bodies, release of epinephrine from the adrenal medulla, and stimulation of the chemoreceptor-trigger zone. (S480)"
2440,T3D0800,Rotenone,"NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial",P28331,"Rotenone works by interfering with the electron transport chain in mitochondria. Specifically, it inhibits the transfer of electrons from iron-sulfur centers in complex I to ubiquinone. This prevents NADH from being converted into usable cellular energy (ATP). (R600)"
2441,T3D0800,Rotenone,NADH-ubiquinone oxidoreductase chain 1,P03886,"Rotenone works by interfering with the electron transport chain in mitochondria. Specifically, it inhibits the transfer of electrons from iron-sulfur centers in complex I to ubiquinone. This prevents NADH from being converted into usable cellular energy (ATP). (R600)"
2442,T3D0800,Rotenone,NADH-ubiquinone oxidoreductase chain 2,P03891,"Rotenone works by interfering with the electron transport chain in mitochondria. Specifically, it inhibits the transfer of electrons from iron-sulfur centers in complex I to ubiquinone. This prevents NADH from being converted into usable cellular energy (ATP). (R600)"
2443,T3D0800,Rotenone,NADH-ubiquinone oxidoreductase chain 3,P03897,"Rotenone works by interfering with the electron transport chain in mitochondria. Specifically, it inhibits the transfer of electrons from iron-sulfur centers in complex I to ubiquinone. This prevents NADH from being converted into usable cellular energy (ATP). (R600)"
2444,T3D0800,Rotenone,NADH-ubiquinone oxidoreductase chain 4,P03905,"Rotenone works by interfering with the electron transport chain in mitochondria. Specifically, it inhibits the transfer of electrons from iron-sulfur centers in complex I to ubiquinone. This prevents NADH from being converted into usable cellular energy (ATP). (R600)"
2445,T3D0146,"1,1,2,2-Tetrachloroethane",DNA,DNA,"1,1,2,2-Tetrachloroethane has been shown to bind to DNA in the liver and several other organs. (R608)"
2446,T3D0207,"2,3,7,8-Tetrachlorodibenzofuran",Aryl hydrocarbon receptor,P35869,"Dibenzofurans bind the aryl hydrocarbon receptor, which increases its ability to activate transcription in the XRE promoter region. This alters the expression of a number of genes. (S285)"
2447,T3D0248,"2,4-Dichlorophenoxyacetic acid",Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2448,T3D0801,Dichlorprop,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2449,T3D0802,"2,4-Dichlorophenoxybutyric acid",Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2450,T3D0803,"2,4,5-Trichlorophenoxyacetic acid",Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2451,T3D0804,2-Methyl-4-chlorophenoxyacetic acid,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2452,T3D0805,4-(4-Chloro-2-methylphenoxy)butanoic acid,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2453,T3D0806,Methylchlorophenoxypropionic acid,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2454,T3D0807,Dicamba,Aryl hydrocarbon receptor,P35869,"Chlorinated dibenzo-p-dioxins cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. This includes 2,3,7,8-tetrachlorodibenzo-p-dioxin's carcinogenicity is thought to be the result of its ability to alter the capacity of both exogenous and endogenous substances to damage the DNA by inducing CYP1A1- and CYP1A2-dependent drug-metabolizing enzymes. (R346)"
2458,T3D0160,"1,1-Dichloroethane",DNA,DNA,"Metabolites of l,l-dichloroethane bind to the DNA. (R688)"
2459,T3D0160,"1,1-Dichloroethane",RNA,RNA,"Metabolites of l,l-dichloroethane bind to the RNA. (R688)"
2461,T3D0808,Paraquat,DNA,DNA,Paraquat competes with the polyamines for an active transport process in lung tissue suggesting the herbicide is capable of binding to some membrane-bound carrier protein for the polyamines.(R716)
2462,T3D0809,Diquat,DNA,DNA,
2463,T3D0163,"1,1,2-Trichloroethane",DNA,DNA,"1,1,2-Trichloroethane and its metabolites bind to DNA. (R717)"
2464,T3D0163,"1,1,2-Trichloroethane",RNA,RNA,"1,1,2-Trichloroethane and its metabolites bind to RNA. (R733)"
2471,T3D0170,"Cresol, para-",Dopamine beta-hydroxylase,P09172,p-Cresol inhibits dopamine beta-hydroxylase. (R845)
2472,T3D0812,Glufosinate,Glutamine synthetase,P15104,"Glufosinate irreversibly inhibits the enzyme glutamine synthetase, which decreases ammonia detoxification. Increased ammonia levels lead to impairment of photorespiration and photosynthesis in plants. (R029)"
2473,T3D0170,"Cresol, para-",Lactoperoxidase,P22079,Lactoperoxidase (LPO) was shown to form a 1:1 complex with p-cresol. (R859)
2474,T3D0170,"Cresol, para-",Myeloperoxidase,P05164,p-Cresol binds near the heme center of myeloperoxidase. (R862)
2476,T3D0815,Angelicin,DNA,DNA,"Upon long wavelength UV irradiation, forms monoadduct with double-stranded DNA and react with unsaturated fatty acids. Inhibits DNA and RNA synthesis and cell replication in Ehrlich ascites tumor cells. (R903)"
2477,T3D0099,Ethylbenzene,Sodium/potassium-transporting ATPase gamma chain,P54710,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2478,T3D0099,Ethylbenzene,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2479,T3D0099,Ethylbenzene,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2480,T3D0099,Ethylbenzene,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2481,T3D0099,Ethylbenzene,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2482,T3D0099,Ethylbenzene,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2483,T3D0099,Ethylbenzene,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2484,T3D0099,Ethylbenzene,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2485,T3D0099,Ethylbenzene,Calcium-transporting ATPase type 2C member 1,P98194,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2486,T3D0099,Ethylbenzene,Calcium-transporting ATPase type 2C member 2,O75185,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2487,T3D0099,Ethylbenzene,Plasma membrane calcium-transporting ATPase 1,P20020,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2488,T3D0099,Ethylbenzene,Plasma membrane calcium-transporting ATPase 2,Q01814,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2489,T3D0099,Ethylbenzene,Plasma membrane calcium-transporting ATPase 3,Q16720,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2490,T3D0099,Ethylbenzene,Plasma membrane calcium-transporting ATPase 4,P23634,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2491,T3D0099,Ethylbenzene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2492,T3D0099,Ethylbenzene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2493,T3D0099,Ethylbenzene,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"Ethybenzene inhibits the activity of the astrocytic membrane ATPases, which helps regulate adequate intercellular levels of ions, nutrients, metabolic intermediates, and precursors in the central nervous system. Thus, this may disturb the ability of the cells to maintain homeostasis. (R590)"
2494,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,Acts as antagonist of proteins with GABA receptor activity. (R903)
2495,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,Acts as antagonist of proteins with GABA receptor activity. (R903)
2496,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit alpha-3,P34903,Acts as antagonist of proteins with GABA receptor activity. (R903)
2497,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit alpha-4,P48169,Acts as antagonist of proteins with GABA receptor activity. (R903)
2498,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,Acts as antagonist of proteins with GABA receptor activity. (R903)
2499,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit alpha-6,Q16445,Acts as antagonist of proteins with GABA receptor activity. (R903)
2500,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit beta-1,P18505,Acts as antagonist of proteins with GABA receptor activity. (R903)
2501,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,Acts as antagonist of proteins with GABA receptor activity. (R903)
2502,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit beta-3,P28472,Acts as antagonist of proteins with GABA receptor activity. (R903)
2503,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit delta,O14764,Acts as antagonist of proteins with GABA receptor activity. (R903)
2504,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit epsilon,P78334,Acts as antagonist of proteins with GABA receptor activity. (R903)
2505,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,Acts as antagonist of proteins with GABA receptor activity. (R903)
2508,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,Acts as antagonist of proteins with GABA receptor activity. (R903)
2510,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,Acts as antagonist of proteins with GABA receptor activity. (R903)
2511,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit pi,O00591,Acts as antagonist of proteins with GABA receptor activity. (R903)
2512,T3D0822,Pimpinellin,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,Acts as antagonist of proteins with GABA receptor activity. (R903)
2513,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit rho-2,P28476,Acts as antagonist of proteins with GABA receptor activity. (R903)
2514,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,Acts as antagonist of proteins with GABA receptor activity. (R903)
2515,T3D0822,Pimpinellin,Gamma-aminobutyric acid receptor subunit theta,Q9UN88,Acts as antagonist of proteins with GABA receptor activity. (R903)
2517,T3D0825,Psoralen,DNA,DNA,"After photoactivation with UV radiation, it appears to bind DNA through single and double-stranded cross-linking. (R903)"
2518,T3D0172,"1,2-Dichlorobenzene",Glutathione S-transferase P,P09211,"1,2-DCB affects the enzymatic activity of both purified and intra-cellular GSTP1-1. (R905)"
2519,T3D0831,Isoimperatorin,Cytochrome P450 1B1,Q16678,Competitive inhibitor of cytochrome P 450 1B1. (R903)
2520,T3D0831,Isoimperatorin,Glutathione S-transferase P,P09211,Potent chemopreventive agents against aflatoxin B1-inducible cyotoxicity in H4IIE cells with a bifunctional effects on glutathione S-transferase and CYP1A. (R903)
2521,T3D0831,Isoimperatorin,Cytochrome P450 1A1,P04798,Potent chemopreventive agents against aflatoxin B1-inducible cyotoxicity in H4IIE cells with a bifunctional effects on glutathione S-transferase and CYP1A. (R903)
2522,T3D0831,Isoimperatorin,Cytochrome P450 1A2,P05177,Potent chemopreventive agents against aflatoxin B1-inducible cyotoxicity in H4IIE cells with a bifunctional effects on glutathione S-transferase and CYP1A. (R903)
2523,T3D0834,Bergamottin,Glutathione S-transferase P,P09211,Potent chemopreventive agents against aflatoxin B1-inducible cyotoxicity in H4IIE cells with a bifunctional effects on glutathione S-transferase and CYP1A. (R903)
2524,T3D0834,Bergamottin,Cytochrome P450 1A1,P04798,Potent chemopreventive agents against aflatoxin B1-inducible cyotoxicity in H4IIE cells with a bifunctional effects on glutathione S-transferase and CYP1A. Potent inhibitor and inactivator of cytochrome P450 1A1-mediated monooxygenase in both murine hepatic microsomes and in a reconstituted system using purified human P450 1A1.(R903)
2525,T3D0173,"1,2-Dichloroethene, trans-",Cytochrome P450 2E1,P05181,"Trans-1,2-dichloroethene inhibits CYP2E1. (R920)"
2526,T3D0836,Xanthotoxin,DNA,DNA,Xanthotoxin plus ultraviolet A (UVA) irradiation induces monoadducts and interstrand cross-links in DNA and therefore can be used to study DNA repair and recombination mechanisms. (R903)
2527,T3D0135,Guthion,Acetylcholinesterase,P22303,"Guthion and its reactive metabolite, gutoxon, directly effect the nervous system by inhibiting acetylcholinesterase (AChE) in the central and peripheral nervous system. Gutoxon reacts with a serine hydroxyl group at the active site of AChE, rendering it largely unreactive. Thus acetylcholine accumulates in the neuromuscular juntions of cholinergic nerves, causing continual stimulation of electrical activity by both muscarinic and nicotinic receptors. Gutoxon has been shown to be the more potent inhibitor. (R904)"
2528,T3D0838,Imperatorin,Tumor necrosis factor,P01375,Imperatorin is a tumor necrosis factor antagonist. (R903)
2529,T3D0838,Imperatorin,DNA,DNA,"In human lymphocyte cultures Imperatorin successively inhibited and accelerated cell proliferation. It showed slight clastogenic effect, the chromosome-damaging effect being expressed mainly in a doubling of the break rate. (R903)"
2530,T3D0842,"6,7-Dihydroxybergamottin",Cytochrome P450 3A4,P08684,CYP3A4 inhibitor (R903)
2531,T3D0843,Isopimpinelin,Cytochrome P450 1A1,P04798,Induces hepatic GSTs and is potent inhibitor of cytochrome P450 1A1/1B1. (R903)
2532,T3D0843,Isopimpinelin,Cytochrome P450 1A2,P05177,Induces hepatic GSTs and is potent inhibitor of cytochrome P450 1A1/1B1. (R903)
2533,T3D0843,Isopimpinelin,DNA,DNA,"Oral administration of isopimpinellin, blocks DNA adduct formation and prevents skin tumor initiation by 7,12-dimehylbenz[a]anthracene in SENCAR mice and in mouse mammary gland. (R903)"
2534,T3D0845,8-Hydroxybergapten,Tyrosinase,P14679,Showed potent tyrosinase inhibition. (R903)
2536,T3D0176,Carbon disulfide,Dopamine beta-hydroxylase,P09172,A primary effect of CS2 exposure is the inhibition of dopamine-beta-hydroxylase (DBH). The ability of CS2 to react with endogenous amines has led to the hypothesis that inhibition of DBH may occur via the formation of dithiocarbamate metabolites which bind to enzymic copper. (R957)
2537,T3D0138,Chlordecone,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
2538,T3D0138,Chlordecone,Androgen receptor,P10275,Chlordecone causes reproductive damage by binding to the androgen receptor. (R966)
2539,T3D0138,Chlordecone,Adenylate cyclase type 1,Q08828,"Chlordecone inhibits calmodulin activated adenylate cyclase, interfering with calmodulin regulated events in central nervous system. (R967)"
2540,T3D0138,Chlordecone,Adenylate cyclase type 3,O60266,"Chlordecone inhibits calmodulin activated adenylate cyclase, interfering with calmodulin regulated events in central nervous system. (R967)"
2541,T3D0138,Chlordecone,Adenylate cyclase type 8,P40145,"Chlordecone inhibits calmodulin activated adenylate cyclase, interfering with calmodulin regulated events in central nervous system. (R967)"
2542,T3D0138,Chlordecone,Calcium-transporting ATPase type 2C member 1,P98194,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2543,T3D0138,Chlordecone,Calcium-transporting ATPase type 2C member 2,O75185,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2544,T3D0138,Chlordecone,Plasma membrane calcium-transporting ATPase 1,P20020,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2545,T3D0138,Chlordecone,Plasma membrane calcium-transporting ATPase 2,Q01814,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2546,T3D0138,Chlordecone,Plasma membrane calcium-transporting ATPase 3,Q16720,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2547,T3D0138,Chlordecone,Plasma membrane calcium-transporting ATPase 4,P23634,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2548,T3D0138,Chlordecone,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2549,T3D0138,Chlordecone,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2550,T3D0138,Chlordecone,Sarcoplasmic/endoplasmic reticulum calcium ATPase 3,Q93084,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2551,T3D0176,Carbon disulfide,Cytochrome P450 1A1,P04798,Carbon disulfide inhibits CYP1A1. (R969)
2552,T3D0176,Carbon disulfide,Cytochrome P450 2E1,P05181,Carbon disulfide inhibits CYP2E1. (R969)
2553,T3D0138,Chlordecone,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2554,T3D0138,Chlordecone,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2555,T3D0138,Chlordecone,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2556,T3D0138,Chlordecone,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2557,T3D0138,Chlordecone,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2558,T3D0138,Chlordecone,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2559,T3D0138,Chlordecone,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2560,T3D0138,Chlordecone,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2561,T3D0855,Mirex,Sodium/potassium-transporting ATPase gamma chain,P54710,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2562,T3D0855,Mirex,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2563,T3D0855,Mirex,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2564,T3D0855,Mirex,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2565,T3D0855,Mirex,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2566,T3D0855,Mirex,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2567,T3D0855,Mirex,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2568,T3D0855,Mirex,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"This organochloride inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2569,T3D0141,"S,S,S-Tributyl phosphorotrithioate",Acetylcholinesterase,P22303,"Like other organophosphate compounds, S,S,S-tributyl phosphorotrithioate causes neurotoxic effects by inhibiting acetylcholinesterase. This results in overstimulation of the central nervous system. (R973)"
2570,T3D0141,"S,S,S-Tributyl phosphorotrithioate",Fatty-acid amide hydrolase,O00519,"S,S,S-Tributyl phosphorotrithioate inhibits an endogenous signaling modulator, fatty acid amide hydrolase, producing secondary neurotoxicity. (R973)"
2571,T3D0141,"S,S,S-Tributyl phosphorotrithioate",Fatty-acid amide hydrolase 2,Q6GMR7,"S,S,S-Tributyl phosphorotrithioate inhibits an endogenous signaling modulator, fatty acid amide hydrolase, producing secondary neurotoxicity. (R973)"
2572,T3D0127,Chlorpyrifos,Fatty-acid amide hydrolase,O00519,"Chlorpyrifos inhibits an endogenous signaling modulator, fatty acid amide hydrolase, producing secondary neurotoxicity. (R973)"
2573,T3D0127,Chlorpyrifos,Fatty-acid amide hydrolase 2,Q6GMR7,"Chlorpyrifos inhibits an endogenous signaling modulator, fatty acid amide hydrolase, producing secondary neurotoxicity. (R973)"
2576,T3D0856,Oxalic Acid,Prothrombin,P00734,"Oxalic acid binds to the prothrombin promoter, inhibiting the formation of thromboxane B2 from arachidonic acid. (R977)(R978)"
2577,T3D0856,Oxalic Acid,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Oxalic acid is a competitive inhibitor of succinate dehydrogenase. (R982)
2578,T3D0856,Oxalic Acid,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Oxalic acid is a competitive inhibitor of succinate dehydrogenase. (R982)
2579,T3D0856,Oxalic Acid,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Oxalic acid is a competitive inhibitor of succinate dehydrogenase. (R982)
2580,T3D0856,Oxalic Acid,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Oxalic acid is a competitive inhibitor of succinate dehydrogenase. (R982)
2582,T3D0182,Phenol,Carbonic anhydrase 2,P00918,"Phenol acts as an effective, low micromolar inhibitor of isozyme hCAII. (R985)"
2583,T3D0182,Phenol,Carbonic anhydrase 1,P00915,"Phenol acts as an effective, low micromolar inhibitor of isozyme hCAI. (R985)"
2584,T3D0182,Phenol,Carbonic anhydrase 3,P07451,"Phenol acts as an effective, low micromolar inhibitor of isozyme hCAIII. (R985)"
2585,T3D0182,Phenol,Carbonic anhydrase 4,P22748,"Phenol acts as an effective, low micromolar inhibitor of isozyme hCAIV. (R985)"
2586,T3D0182,Phenol,Carbonic anhydrase 9,Q16790,"Phenol acts as an effective, low micromolar inhibitor of isozyme hCAIX. (R985)"
2587,T3D0182,Phenol,Carbonic anhydrase 12,O43570,"Phenol acts as an effective, low micromolar inhibitor of isozyme hCAXII. (R985)"
2588,T3D0182,Phenol,Carbonic anhydrase 14,Q9ULX7,"Phenol acts as an effective, low micromolar inhibitor of isozyme hCAXIV. (R985)"
2589,T3D0182,Phenol,Carbonic anhydrase 13,Q8N1Q1,"Phenol acts as an effective, low inhibitor(in the millimolar range) of isozyme hCAXIV. (R985)"
2590,T3D0182,Phenol,"Carbonic anhydrase 5A, mitochondrial",P35218,"Phenol acts as an effective, low inhibitor(in the millimolar range) of isozyme hCAVA. (R985)"
2591,T3D0182,Phenol,"Carbonic anhydrase 5B, mitochondrial",Q9Y2D0,"Phenol acts as an effective, low inhibitor(in the millimolar range) of isozyme hCAVB. (R985)"
2592,T3D0182,Phenol,Carbonic anhydrase 6,P23280,"Phenol acts as an effective, low inhibitor(in the millimolar range) of isozyme hCAVI. (R985)"
2593,T3D0182,Phenol,Carbonic anhydrase 7,P43166,"Phenol acts as an effective, low inhibitor(in the millimolar range) of isozyme hCAVII. (R985)"
2595,T3D0148,"Hexachlorocyclohexane, technical Grade",Gamma-aminobutyric acid receptor subunit epsilon,P78334,"Hexachlorocyclohexane is a neurotoxin that interferes with GABA neurotransmitter function by interacting with the GABA-A receptor-chloride channel complex at the picrotoxin binding site, causing over stimulation of the central nervous system. (R186)"
2599,T3D0857,Cucurbitacin I,Signal transducer and activator of transcription 3,P40763,Cucurbitacin I is an inhibitor of STAT3. (R996)
2600,T3D0857,Cucurbitacin I,Tyrosine-protein kinase JAK2,O60674,Cucurbitacin I is an inhibitor of JAK2. (R996)
2601,T3D0143,Polybrominated biphenyls,Aryl hydrocarbon receptor,P35869,"PBBs bind to and activate the aryl hydrocarbon receptor (AhR), which in turn initiates the transcriptional upregulation of a number of genes, affecting biochemical and endocrine pathways, cell cycle regulation, morphogenesis, oxidative stress response, and various other processes. This results in the numerous toxic responses characteristic of PBBs. Some of the known induced genes include the cytochrome P-450-dependent monooxygenases CYP1A1 and CYP1A2. (R994)"
2602,T3D0151,"DDD, O,P'-",Sodium channel protein type 1 subunit alpha,P35498,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2603,T3D0151,"DDD, O,P'-",Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2604,T3D0151,"DDD, O,P'-",Sodium channel protein type 11 subunit alpha,Q9UI33,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2605,T3D0151,"DDD, O,P'-",Sodium channel protein type 2 subunit alpha,Q99250,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2606,T3D0151,"DDD, O,P'-",Sodium channel protein type 3 subunit alpha,Q9NY46,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2607,T3D0151,"DDD, O,P'-",Sodium channel protein type 4 subunit alpha,P35499,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2608,T3D0151,"DDD, O,P'-",Sodium channel protein type 5 subunit alpha,Q14524,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2609,T3D0151,"DDD, O,P'-",Sodium channel protein type 7 subunit alpha,Q01118,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2610,T3D0151,"DDD, O,P'-",Sodium channel protein type 8 subunit alpha,Q9UQD0,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2611,T3D0151,"DDD, O,P'-",Sodium channel protein type 9 subunit alpha,Q15858,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2612,T3D0151,"DDD, O,P'-",Sodium channel subunit beta-1,Q07699,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2613,T3D0151,"DDD, O,P'-",Sodium channel subunit beta-2,O60939,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2614,T3D0151,"DDD, O,P'-",Sodium channel subunit beta-3,Q9NY72,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2615,T3D0151,"DDD, O,P'-",Sodium channel subunit beta-4,Q8IWT1,"DDD inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2616,T3D0158,2-Methylnaphthalene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2617,T3D0161,Acenaphthene,DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2618,T3D0174,"Indeno(1,2,3-cd)pyrene",DNA,DNA,"The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (R028, R060, R068, R073)"
2621,T3D0144,Dicofol,Sodium channel protein type 1 subunit alpha,P35498,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2622,T3D0144,Dicofol,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2623,T3D0144,Dicofol,Sodium channel protein type 11 subunit alpha,Q9UI33,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2624,T3D0144,Dicofol,Sodium channel protein type 2 subunit alpha,Q99250,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2625,T3D0144,Dicofol,Sodium channel protein type 3 subunit alpha,Q9NY46,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2626,T3D0144,Dicofol,Sodium channel protein type 4 subunit alpha,P35499,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2627,T3D0144,Dicofol,Sodium channel protein type 5 subunit alpha,Q14524,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2628,T3D0144,Dicofol,Sodium channel protein type 7 subunit alpha,Q01118,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2629,T3D0144,Dicofol,Sodium channel protein type 8 subunit alpha,Q9UQD0,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2630,T3D0144,Dicofol,Sodium channel protein type 9 subunit alpha,Q15858,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2631,T3D0144,Dicofol,Sodium channel subunit beta-1,Q07699,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2632,T3D0144,Dicofol,Sodium channel subunit beta-2,O60939,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2633,T3D0144,Dicofol,Sodium channel subunit beta-3,Q9NY72,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2634,T3D0144,Dicofol,Sodium channel subunit beta-4,Q8IWT1,"Difocol inhibits the inactivation of voltaged-gated sodium channels. The channels activate (open) normally but are inactivated (closed) slowly, thus interfering with the active transport of sodium out of the nerve axon during repolarization and resulting in a state of hyperexcitability. (R252)"
2635,T3D0144,Dicofol,Cytochrome P450 19A1,P11511,Difocol may alter sex hormone metabolism by directly inhibiting cytochrome P-450 19A1. (R1002)
2636,T3D0144,Dicofol,Transthyretin,P02766,"Difocol is able to competitively bind transthyretin, which lowers plasma thyroid hormone levels. (R1003)"
2637,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 1",P11166,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2638,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 10",O95528,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2639,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 11",Q9BYW1,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2640,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 12",Q8TD20,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2641,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 2",P11168,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2642,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 3",P11169,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2643,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 4",P14672,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2645,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 5",P22732,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2646,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 6",Q9UGQ3,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2647,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 7",Q6PXP3,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2648,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 8",Q9NY64,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2649,T3D0859,Linamarin,"Solute carrier family 2, facilitated glucose transporter member 9",Q9NRM0,"Linamarin binds to GLUT and enter cells. Transported linamarin directly damages both neural PC12 and hepatic Hepa1 cells, causing cell death. (R1007)"
2650,T3D0264,Methyl parathion,Acetylcholinesterase,P22303,"The active metabolite of methyl parathion, methyl paraoxon, inactivates acetylcholinesterase by phosphorylating the active site of the enzyme, thus inhibiting its activity in the nervous system and at the motor end-plate. As a result, the neurotransmitter acetylcholine accumulates in the nerve synapse or neuromuscular junction, producing overstimulation of cholinergic end organs. (R1006)"
2651,T3D0145,Parathion,Acetylcholinesterase,P22303,"The active metabolite of parathion, paraoxon, inactivates acetylcholinesterase by phosphorylating the active site of the enzyme, thus inhibiting its activity in the nervous system and at the motor end-plate. As a result, the neurotransmitter acetylcholine accumulates in the nerve synapse or neuromuscular junction, producing overstimulation of cholinergic end organs. (R1006)"
2654,T3D0863,"Xylene, meta-",Cytochrome P450 2E1,P05181,Certain metabolites of xylene have been shown to inhibit pulmonary mixed-function oxidases. (R322)
2655,T3D0863,"Xylene, meta-",Cytochrome P450 4B1,P13584,Certain metabolites of xylene have been shown to inhibit pulmonary mixed-function oxidases. (R322)
2656,T3D0864,"Xylene, ortho-",Cytochrome P450 2E1,P05181,Certain metabolites of xylene have been shown to inhibit pulmonary mixed-function oxidases. (R322) 
2657,T3D0864,"Xylene, ortho-",Cytochrome P450 4B1,P13584,Certain metabolites of xylene have been shown to inhibit pulmonary mixed-function oxidases. (R322) 
2658,T3D0261,"2,6-Dinitrotoluene",DNA,DNA,"Some metabolites of 2,6-DNT can covalently bind to DNA. (R511)"
2659,T3D0261,"2,6-Dinitrotoluene",RNA,RNA,"Some metabolites of 2,6-DNT can covalently bind to RNA. (R511)"
2660,T3D0222,"2,4,5-Trichlorophenol",Acetylcholinesterase,P22303,"2,4,6-trichlorophenol (2,4,6-TCP) has been identified to hemolyze washed human erythrocytes and inhibit acetylcholinesterase (AchE) activities in the erythrocyte membrane (R318)."
2661,T3D0187,Aluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
2662,T3D0187,Aluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
2663,T3D0187,Aluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
2664,T3D0172,"1,2-Dichlorobenzene",DNA,DNA,"1,2-DCB was found to covalently bind to DNA, RNA, and proteins of liver, kidney, lung, and stomach. (R677)"
2665,T3D0172,"1,2-Dichlorobenzene",RNA,RNA,"1,2-DCB was found to covalently bind to DNA, RNA, and proteins of liver, kidney, lung, and stomach. (R677)"
2667,T3D0180,Palladium,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
2672,T3D0180,Palladium,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
2673,T3D0180,Palladium,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
2674,T3D0180,Palladium,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
2675,T3D0180,Palladium,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
2676,T3D0892,"2-(4,5-Dimethyl-1,3-dioxolan-2-yl)phenyl-N-methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2677,T3D0893,"2,3,5-Trimethylphenyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2678,T3D0894,"2,3-Dichlorobenzyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2679,T3D0895,"2,4-Dimethyl-1,3-dithiolane-2-carboxaldehyde O-(methylcarbamoyl)oxime",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2680,T3D0896,"2-Chloro-4,5-xylyl N-hydroxy-N-methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2681,T3D0897,2-Cyclopentylphenyl methylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2682,T3D0898,2-Hydroxyphenyl methylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2683,T3D0899,3-(4-Chlorophenyl)-1-(4-chlorophenylcarbamoyl)-2-pyrazoline,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2684,T3D0900,"3,4-Dichlorobenzyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2685,T3D0901,"3,5-Diisopropylphenyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2686,T3D0902,"3,5-Xylyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2687,T3D0903,3-Hydroxycarbofuran,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2688,T3D0904,3-Iodo-2-propynyl butyl carbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2689,T3D0905,3-Ketocarbofuran,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2690,T3D0906,3-tert-Butylphenyl sec-butylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2691,T3D0907,"4-(Methylamino)-3,5-xylyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2692,T3D0908,4-(Methylthio)-m-tolyl methylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2693,T3D0909,"4-Amino-3,5-xylyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2694,T3D0910,4-Chlorophenyl-N-methylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2695,T3D0911,4-Ethylthiophenyl methylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2696,T3D0912,"4-Methylformamido-3,5-xylyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2697,T3D0913,"5,6,7,8-Tetrahydro-1-naphthyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2698,T3D0914,"6-Chloro-3,4-xylyl methylcarbamate",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2699,T3D0915,6-Methyl-2-propyl-4-pyrimidinyl dimethylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2700,T3D0916,Alanycarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2701,T3D0917,Alcamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2702,T3D0918,Aldicarb sulfoxide,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2703,T3D0919,Aldicarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2704,T3D0920,Aldoxycarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2705,T3D0921,Allyxycarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2706,T3D0922,Aminocarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2707,T3D0923,Asulam,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2708,T3D0924,"Asulam, sodium salt",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2709,T3D0925,Barban,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2711,T3D0926,Bendiocarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2712,T3D0927,Benfuracarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2713,T3D0928,Benomyl,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2714,T3D0929,Benthiavalicarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2715,T3D0930,Benthiavalicarb-isopropyl,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2716,T3D0931,Betamix,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2717,T3D0932,"Biscarbofuran N,N'-disulfide",Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2718,T3D0933,Bufencarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2720,T3D0934,Bufencarb-1,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2721,T3D0935,Bufencarb-2,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2722,T3D0936,Butacarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2723,T3D0937,Butocarboxim,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2724,T3D0938,Butoxycarboxim,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2725,T3D0939,Carbanolate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2726,T3D0940,Carbaril,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2727,T3D0941,Carbasulam,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2728,T3D0942,Carbendazim,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2729,T3D0943,Carbetamide,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2730,T3D0944,Carbofuran,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2731,T3D0945,Carbosulfan,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2732,T3D0946,Carboxazole,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2733,T3D0947,Chlorbufam,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2734,T3D0948,Chlorprocarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2735,T3D0949,Chlorpropham,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2736,T3D0950,Cloethocarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2737,T3D0951,Cycloate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2738,T3D0952,Cypendazole,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2739,T3D0953,Debacarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2740,T3D0954,Decarbofuran,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2741,T3D0955,Desmedipham,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2743,T3D0956,Di-allate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2744,T3D0957,Dichlormate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2745,T3D0958,Dicresyl,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2746,T3D0959,Diethofencarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2747,T3D0960,Dimetan,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2748,T3D0961,Dimetilan,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2749,T3D0962,Dioxacarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2750,T3D0963,Dipropylcarbamothioic acid S-ethyl ester,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2751,T3D0964,Ethiofencarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2752,T3D0965,Ethylene thiuram monosulfide,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2753,T3D0966,Fenasulam,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2754,T3D0967,Fenethacarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2755,T3D0968,Fenobucarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2756,T3D0969,Fenoxycarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2757,T3D0970,Formetanate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2758,T3D0971,Formetanate hydrochloride,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2759,T3D0972,Formparanate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2760,T3D0973,Fosamine,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2761,T3D0974,Furathiocarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2762,T3D0975,Hyquincarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2763,T3D0976,Isolan,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2764,T3D0977,Isoprocarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2765,T3D0978,Karbutilate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2766,T3D0979,m-Cumenyl methylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2767,T3D0980,Mecarbinzid,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2768,T3D0981,Methiocarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2769,T3D0982,Methiocarb sulfone,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2770,T3D0983,Methiocarb sulfoxide,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2772,T3D0984,Methomyl,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2773,T3D0985,Metolcarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2774,T3D0986,Mexacarbate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2775,T3D0987,Mobam,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2776,T3D0988,Molinate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2777,T3D0989,Nitrilacarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2778,T3D0990,o-(2-Propynyloxy)phenyl methylcarbamate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2779,T3D0991,Oms 22,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2780,T3D0992,Oxamyl,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2781,T3D0993,Pebulate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2782,T3D0994,Phenmedipham,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2784,T3D0995,Pirimicarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2785,T3D0996,Potassium asulam,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2786,T3D0997,Primor,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2787,T3D0998,Promacyl,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2788,T3D0999,Promecarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2790,T3D1000,Propamocarb hydrochloride,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2791,T3D1001,Propamocarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2792,T3D1002,Propham,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2794,T3D1003,Propoxur,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2795,T3D1004,Proximphan,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2796,T3D1005,Pyrolan,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2797,T3D1006,Sulfallate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2798,T3D1007,Sulfocarbathione,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2799,T3D1008,Swep,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2800,T3D1009,Tazimcarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2801,T3D1010,Terbucarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2802,T3D1011,Thiobencarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2803,T3D1012,Thiocarboxime,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2804,T3D1013,Thiodicarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2805,T3D1014,Thiofanox,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2806,T3D1015,Tillam sulfoxide,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2807,T3D1016,Tiocarbazil,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2808,T3D1017,Triallate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2809,T3D1018,Trimethacarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2811,T3D1020,Vernolate,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2812,T3D1021,Xylylcarb,Cholinesterase,P06276,"Like the organophosphates, their mode of action is inhibition of cholinesterase enzymes, affecting nerve impulse transmission. (S059)"
2813,T3D0214,Silver,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077) "
2814,T3D0214,Silver,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077) "
2815,T3D0214,Silver,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077) "
2816,T3D0214,Silver,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077) "
2817,T3D0214,Silver,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077) "
2818,T3D0214,Silver,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077) "
2819,T3D0214,Silver,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077) "
2820,T3D0214,Silver,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077) "
2821,T3D0214,Silver,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080) "
2822,T3D0214,Silver,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080) "
2823,T3D0214,Silver,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080) "
2824,T3D0214,Silver,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080) "
2825,T3D0214,Silver,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080) "
2826,T3D0214,Silver,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080) "
2827,T3D0214,Silver,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080) "
2828,T3D0214,Silver,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080) "
2829,T3D1024,Allethrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2830,T3D1024,Allethrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2831,T3D1024,Allethrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2832,T3D1024,Allethrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2833,T3D1024,Allethrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2834,T3D1024,Allethrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2835,T3D1024,Allethrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2836,T3D1024,Allethrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2837,T3D1024,Allethrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2838,T3D1024,Allethrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2839,T3D1024,Allethrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2840,T3D1024,Allethrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2841,T3D1024,Allethrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2842,T3D1024,Allethrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2843,T3D1024,Allethrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2844,T3D1024,Allethrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2845,T3D1024,Allethrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2846,T3D1024,Allethrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2847,T3D1024,Allethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2848,T3D1024,Allethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2849,T3D1025,Cismethrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2850,T3D1025,Cismethrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2851,T3D1025,Cismethrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2852,T3D1025,Cismethrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2853,T3D1025,Cismethrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2854,T3D1025,Cismethrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2855,T3D1025,Cismethrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2856,T3D1025,Cismethrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2857,T3D1025,Cismethrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2858,T3D1025,Cismethrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2859,T3D1025,Cismethrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2860,T3D1025,Cismethrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2861,T3D1025,Cismethrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2862,T3D1025,Cismethrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2863,T3D1025,Cismethrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2864,T3D1025,Cismethrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2865,T3D1025,Cismethrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2866,T3D1025,Cismethrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2867,T3D1025,Cismethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2868,T3D1025,Cismethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2869,T3D1026,Phenothrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2870,T3D1026,Phenothrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2871,T3D1026,Phenothrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2872,T3D1026,Phenothrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2873,T3D1026,Phenothrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2874,T3D1026,Phenothrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2875,T3D1026,Phenothrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2876,T3D1026,Phenothrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2877,T3D1026,Phenothrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2878,T3D1026,Phenothrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2879,T3D1026,Phenothrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2880,T3D1026,Phenothrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2881,T3D1026,Phenothrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2882,T3D1026,Phenothrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2883,T3D1026,Phenothrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2884,T3D1026,Phenothrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2885,T3D1026,Phenothrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2886,T3D1026,Phenothrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2887,T3D1026,Phenothrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2888,T3D1026,Phenothrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2889,T3D0233,Pyrethrum,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2890,T3D0233,Pyrethrum,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2891,T3D0233,Pyrethrum,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2892,T3D0233,Pyrethrum,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2893,T3D0233,Pyrethrum,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2894,T3D0233,Pyrethrum,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2895,T3D0233,Pyrethrum,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2896,T3D0233,Pyrethrum,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2897,T3D0233,Pyrethrum,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2898,T3D0233,Pyrethrum,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2899,T3D0233,Pyrethrum,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2900,T3D0233,Pyrethrum,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2901,T3D0233,Pyrethrum,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2902,T3D0233,Pyrethrum,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2903,T3D0233,Pyrethrum,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2904,T3D0233,Pyrethrum,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2905,T3D0233,Pyrethrum,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2906,T3D0233,Pyrethrum,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2907,T3D0233,Pyrethrum,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2908,T3D0233,Pyrethrum,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2909,T3D1027,Resmethrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2910,T3D1027,Resmethrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2911,T3D1027,Resmethrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2912,T3D1027,Resmethrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2913,T3D1027,Resmethrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2914,T3D1027,Resmethrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2915,T3D1027,Resmethrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2916,T3D1027,Resmethrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2917,T3D1027,Resmethrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2918,T3D1027,Resmethrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2919,T3D1027,Resmethrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2920,T3D1027,Resmethrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2921,T3D1027,Resmethrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2922,T3D1027,Resmethrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2923,T3D1027,Resmethrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2924,T3D1027,Resmethrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2925,T3D1027,Resmethrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2926,T3D1027,Resmethrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2927,T3D1027,Resmethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2928,T3D1027,Resmethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2929,T3D1028,Tetramethrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2930,T3D1028,Tetramethrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2931,T3D1028,Tetramethrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2932,T3D1028,Tetramethrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2933,T3D1028,Tetramethrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2934,T3D1028,Tetramethrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2935,T3D1028,Tetramethrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2936,T3D1028,Tetramethrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2937,T3D1028,Tetramethrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2938,T3D1028,Tetramethrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2939,T3D1028,Tetramethrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2940,T3D1028,Tetramethrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2941,T3D1028,Tetramethrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2942,T3D1028,Tetramethrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2943,T3D1028,Tetramethrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2944,T3D1028,Tetramethrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2945,T3D1028,Tetramethrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2946,T3D1028,Tetramethrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2947,T3D1028,Tetramethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2948,T3D1028,Tetramethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2949,T3D1029,Acrinathrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2950,T3D1029,Acrinathrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2951,T3D1029,Acrinathrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2952,T3D1029,Acrinathrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2953,T3D1029,Acrinathrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2954,T3D1029,Acrinathrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2955,T3D1029,Acrinathrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2956,T3D1029,Acrinathrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2957,T3D1029,Acrinathrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2958,T3D1029,Acrinathrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2959,T3D1029,Acrinathrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2960,T3D1029,Acrinathrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2961,T3D1029,Acrinathrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2962,T3D1029,Acrinathrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2963,T3D1029,Acrinathrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2964,T3D1029,Acrinathrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2965,T3D1029,Acrinathrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2966,T3D1029,Acrinathrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2967,T3D1029,Acrinathrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2968,T3D1029,Acrinathrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2969,T3D1030,Cycloprothrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2970,T3D1030,Cycloprothrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2971,T3D1030,Cycloprothrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2972,T3D1030,Cycloprothrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2973,T3D1030,Cycloprothrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2974,T3D1030,Cycloprothrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2975,T3D1030,Cycloprothrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2976,T3D1030,Cycloprothrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2977,T3D1030,Cycloprothrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2978,T3D1030,Cycloprothrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2979,T3D1030,Cycloprothrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2980,T3D1030,Cycloprothrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2981,T3D1030,Cycloprothrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2982,T3D1030,Cycloprothrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2983,T3D1030,Cycloprothrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2984,T3D1030,Cycloprothrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
2985,T3D1030,Cycloprothrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2986,T3D1030,Cycloprothrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2987,T3D1030,Cycloprothrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2988,T3D1030,Cycloprothrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2989,T3D1031,Cyfluthrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2990,T3D1031,Cyfluthrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2991,T3D1031,Cyfluthrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2992,T3D1031,Cyfluthrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2993,T3D1031,Cyfluthrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2994,T3D1031,Cyfluthrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2995,T3D1031,Cyfluthrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2996,T3D1031,Cyfluthrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2997,T3D1031,Cyfluthrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2998,T3D1031,Cyfluthrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
2999,T3D1031,Cyfluthrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3000,T3D1031,Cyfluthrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3001,T3D1031,Cyfluthrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3002,T3D1031,Cyfluthrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3003,T3D1031,Cyfluthrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3004,T3D1031,Cyfluthrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3005,T3D1031,Cyfluthrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3006,T3D1031,Cyfluthrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3007,T3D1031,Cyfluthrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3008,T3D1031,Cyfluthrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3009,T3D1032,Cyhalothrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3010,T3D1032,Cyhalothrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3011,T3D1032,Cyhalothrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3012,T3D1032,Cyhalothrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3013,T3D1032,Cyhalothrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3014,T3D1032,Cyhalothrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3015,T3D1032,Cyhalothrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3016,T3D1032,Cyhalothrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3017,T3D1032,Cyhalothrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3018,T3D1032,Cyhalothrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3019,T3D1032,Cyhalothrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3020,T3D1032,Cyhalothrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3021,T3D1032,Cyhalothrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3022,T3D1032,Cyhalothrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3023,T3D1032,Cyhalothrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3024,T3D1032,Cyhalothrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3025,T3D1032,Cyhalothrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3026,T3D1032,Cyhalothrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3027,T3D1032,Cyhalothrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3028,T3D1032,Cyhalothrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3029,T3D1033,Cyphenothrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3030,T3D1033,Cyphenothrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3031,T3D1033,Cyphenothrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3032,T3D1033,Cyphenothrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3033,T3D1033,Cyphenothrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3034,T3D1033,Cyphenothrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3035,T3D1033,Cyphenothrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3036,T3D1033,Cyphenothrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3037,T3D1033,Cyphenothrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3038,T3D1033,Cyphenothrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3039,T3D1033,Cyphenothrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3040,T3D1033,Cyphenothrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3041,T3D1033,Cyphenothrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3042,T3D1033,Cyphenothrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3043,T3D1033,Cyphenothrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3044,T3D1033,Cyphenothrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3045,T3D1033,Cyphenothrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3046,T3D1033,Cyphenothrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3047,T3D1033,Cyphenothrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3048,T3D1033,Cyphenothrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3049,T3D1034,Cypermethrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3050,T3D1034,Cypermethrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3051,T3D1034,Cypermethrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3052,T3D1034,Cypermethrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3053,T3D1034,Cypermethrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3054,T3D1034,Cypermethrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3055,T3D1034,Cypermethrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3056,T3D1034,Cypermethrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3057,T3D1034,Cypermethrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3058,T3D1034,Cypermethrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3059,T3D1034,Cypermethrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3060,T3D1034,Cypermethrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3061,T3D1034,Cypermethrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3062,T3D1034,Cypermethrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3063,T3D1034,Cypermethrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3064,T3D1034,Cypermethrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3065,T3D1034,Cypermethrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3066,T3D1034,Cypermethrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3067,T3D1034,Cypermethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3068,T3D1034,Cypermethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3069,T3D1035,Deltamethrin,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3070,T3D1035,Deltamethrin,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3071,T3D1035,Deltamethrin,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3072,T3D1035,Deltamethrin,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3073,T3D1035,Deltamethrin,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3074,T3D1035,Deltamethrin,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3075,T3D1035,Deltamethrin,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3076,T3D1035,Deltamethrin,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3077,T3D1035,Deltamethrin,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3078,T3D1035,Deltamethrin,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3079,T3D1035,Deltamethrin,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3080,T3D1035,Deltamethrin,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3081,T3D1035,Deltamethrin,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3082,T3D1035,Deltamethrin,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3083,T3D1035,Deltamethrin,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3084,T3D1035,Deltamethrin,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3085,T3D1035,Deltamethrin,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3086,T3D1035,Deltamethrin,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3087,T3D1035,Deltamethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3088,T3D1035,Deltamethrin,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3089,T3D1036,Esfenvalerate,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3090,T3D1036,Esfenvalerate,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3091,T3D1036,Esfenvalerate,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3092,T3D1036,Esfenvalerate,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3093,T3D1036,Esfenvalerate,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3094,T3D1036,Esfenvalerate,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3095,T3D1036,Esfenvalerate,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3096,T3D1036,Esfenvalerate,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3097,T3D1036,Esfenvalerate,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3098,T3D1036,Esfenvalerate,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3099,T3D1036,Esfenvalerate,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3100,T3D1036,Esfenvalerate,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3101,T3D1036,Esfenvalerate,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3102,T3D1036,Esfenvalerate,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3103,T3D1036,Esfenvalerate,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3104,T3D1036,Esfenvalerate,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3105,T3D1036,Esfenvalerate,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3106,T3D1036,Esfenvalerate,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3107,T3D1036,Esfenvalerate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3108,T3D1036,Esfenvalerate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3109,T3D1037,Fenvalerate,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3110,T3D1037,Fenvalerate,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3111,T3D1037,Fenvalerate,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3112,T3D1037,Fenvalerate,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3113,T3D1037,Fenvalerate,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3114,T3D1037,Fenvalerate,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3115,T3D1037,Fenvalerate,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3116,T3D1037,Fenvalerate,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3117,T3D1037,Fenvalerate,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3118,T3D1037,Fenvalerate,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3119,T3D1037,Fenvalerate,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3120,T3D1037,Fenvalerate,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3121,T3D1037,Fenvalerate,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3122,T3D1037,Fenvalerate,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3123,T3D1037,Fenvalerate,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3124,T3D1037,Fenvalerate,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3125,T3D1037,Fenvalerate,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3126,T3D1037,Fenvalerate,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3127,T3D1037,Fenvalerate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3128,T3D1037,Fenvalerate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3129,T3D1038,Flucynthrate,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3130,T3D1038,Flucynthrate,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3131,T3D1038,Flucynthrate,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3132,T3D1038,Flucynthrate,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3133,T3D1038,Flucynthrate,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3134,T3D1038,Flucynthrate,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3135,T3D1038,Flucynthrate,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3136,T3D1038,Flucynthrate,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3137,T3D1038,Flucynthrate,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3138,T3D1038,Flucynthrate,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3139,T3D1038,Flucynthrate,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3140,T3D1038,Flucynthrate,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3141,T3D1038,Flucynthrate,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3142,T3D1038,Flucynthrate,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3143,T3D1038,Flucynthrate,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3144,T3D1038,Flucynthrate,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3145,T3D1038,Flucynthrate,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3146,T3D1038,Flucynthrate,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3147,T3D1038,Flucynthrate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3148,T3D1038,Flucynthrate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3149,T3D1039,Fluvalinate,Sodium channel protein type 1 subunit alpha,P35498,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3150,T3D1039,Fluvalinate,Sodium channel protein type 10 subunit alpha,Q9Y5Y9,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3151,T3D1039,Fluvalinate,Sodium channel protein type 11 subunit alpha,Q9UI33,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3152,T3D1039,Fluvalinate,Sodium channel protein type 2 subunit alpha,Q99250,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3153,T3D1039,Fluvalinate,Sodium channel protein type 3 subunit alpha,Q9NY46,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3154,T3D1039,Fluvalinate,Sodium channel protein type 4 subunit alpha,P35499,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3155,T3D1039,Fluvalinate,Sodium channel protein type 5 subunit alpha,Q14524,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3156,T3D1039,Fluvalinate,Sodium channel protein type 7 subunit alpha,Q01118,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3157,T3D1039,Fluvalinate,Sodium channel protein type 8 subunit alpha,Q9UQD0,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3158,T3D1039,Fluvalinate,Sodium channel protein type 9 subunit alpha,Q15858,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3159,T3D1039,Fluvalinate,Sodium channel subunit beta-1,Q07699,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3160,T3D1039,Fluvalinate,Sodium channel subunit beta-2,O60939,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3161,T3D1039,Fluvalinate,Sodium channel subunit beta-3,Q9NY72,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3162,T3D1039,Fluvalinate,Sodium channel subunit beta-4,Q8IWT1,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3163,T3D1039,Fluvalinate,Calcium release-activated calcium channel protein 1,Q96D31,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3164,T3D1039,Fluvalinate,Calcium-activated potassium channel subunit alpha 1,Q12791,"This pyrethroid inhibits Na+/K+ ATPase and Ca2+ and Mg2+ ATPase, which are essential for the transport of calcium across membranes. This results in the accumulation of intracellular free calcium ions, which promotes release of neurotransmitters from storage vesicles, the subsequent depolarization of adjacent neurons, and the propagation of stimuli throughout the central nervous system. (R029)"
3165,T3D1039,Fluvalinate,Calcium-transporting ATPase type 2C member 1,P98194,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3166,T3D1039,Fluvalinate,Calcium-transporting ATPase type 2C member 2,O75185,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3167,T3D1039,Fluvalinate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 2,P16615,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3168,T3D1039,Fluvalinate,Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,O14983,"This pyrethroid exerts its profound effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. This pyrethroid is a axonic poison that block the closing of the sodium gates in the nerves, and, thus, prolongs the return of the membrane potential to its resting state leading to hyperactivity of the nervous system which can result in paralysis and/or death. Type I Pyrethroid esters (lacking the alpha-cyano substituents) affect sodium channels in nerve membranes, causing repetitive (sensory, motor) neuronal discharge and a prolonged negative afterpotential, the effects being quite similar to those produced by DDT (S135, S149)."
3169,T3D1040,Ivermectin,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3170,T3D1040,Ivermectin,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3171,T3D1040,Ivermectin,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3172,T3D1040,Ivermectin,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3173,T3D1040,Ivermectin,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3174,T3D1040,Ivermectin,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3175,T3D1040,Ivermectin,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3176,T3D1040,Ivermectin,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3177,T3D1040,Ivermectin,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3178,T3D1040,Ivermectin,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3179,T3D1041,Avermectin B1a,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3180,T3D1041,Avermectin B1a,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3181,T3D1041,Avermectin B1a,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3182,T3D1041,Avermectin B1a,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3183,T3D1041,Avermectin B1a,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3184,T3D1041,Avermectin B1a,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3185,T3D1041,Avermectin B1a,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3186,T3D1041,Avermectin B1a,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3187,T3D1041,Avermectin B1a,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3188,T3D1041,Avermectin B1a,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3189,T3D1042,Avermectin B1b,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3190,T3D1042,Avermectin B1b,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3191,T3D1042,Avermectin B1b,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3192,T3D1042,Avermectin B1b,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3193,T3D1042,Avermectin B1b,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3194,T3D1042,Avermectin B1b,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3195,T3D1042,Avermectin B1b,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3196,T3D1042,Avermectin B1b,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3197,T3D1042,Avermectin B1b,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3198,T3D1042,Avermectin B1b,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3199,T3D1043,Emamectin B1a,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3200,T3D1043,Emamectin B1a,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3201,T3D1043,Emamectin B1a,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3202,T3D1043,Emamectin B1a,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3203,T3D1043,Emamectin B1a,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3204,T3D1043,Emamectin B1a,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3205,T3D1043,Emamectin B1a,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3206,T3D1043,Emamectin B1a,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3207,T3D1043,Emamectin B1a,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3208,T3D1043,Emamectin B1a,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3209,T3D1044,Emamectin B1b,Gamma-aminobutyric acid receptor subunit gamma-2,P18507,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3210,T3D1044,Emamectin B1b,Gamma-aminobutyric-acid receptor subunit alpha-1,P14867,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3211,T3D1044,Emamectin B1b,Gamma-aminobutyric acid receptor subunit rho-2,P28476,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3212,T3D1044,Emamectin B1b,Gamma-aminobutyric acid receptor subunit gamma-1,Q8N1C3,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3213,T3D1044,Emamectin B1b,Gamma-aminobutyric-acid receptor subunit beta-2,P47870,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3214,T3D1044,Emamectin B1b,Gamma-aminobutyric-acid receptor subunit alpha-2,P47869,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3215,T3D1044,Emamectin B1b,Gamma-aminobutyric acid receptor subunit rho-3,A8MPY1,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3216,T3D1044,Emamectin B1b,Gamma-aminobutyric-acid receptor subunit rho-1,P24046,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3217,T3D1044,Emamectin B1b,Gamma-aminobutyric-acid receptor subunit alpha-5,P31644,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3218,T3D1044,Emamectin B1b,Gamma-aminobutyric acid receptor subunit gamma-3,Q99928,"It has low solubility in water and extensive non-specific binding. It opens GABA-insensitive chloride channels, reducing membrane resistance and increasing conductance inward. (R029)"
3219,T3D0198,Vanadium,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
3220,T3D0198,Vanadium,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
3221,T3D0198,Vanadium,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
3222,T3D0198,Vanadium,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
3223,T3D0198,Vanadium,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
3224,T3D0198,Vanadium,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
3225,T3D0198,Vanadium,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
3226,T3D0198,Vanadium,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
3227,T3D0198,Vanadium,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3228,T3D0198,Vanadium,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3229,T3D0198,Vanadium,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3230,T3D0198,Vanadium,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3231,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3232,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3233,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3234,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3235,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3236,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3237,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3238,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3239,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3241,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3242,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3243,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3244,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3245,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3246,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3247,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3248,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3249,T3D0198,Vanadium,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3250,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3251,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3252,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3253,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3255,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3256,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3257,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3258,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3259,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3260,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3261,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3263,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3264,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3265,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3266,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3267,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3268,T3D0198,Vanadium,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
3269,T3D1045,2-[(2E)-2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3270,T3D1045,2-[(2E)-2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3271,T3D1045,2-[(2E)-2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3272,T3D1045,2-[(2E)-2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3273,T3D1045,2-[(2E)-2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3274,T3D1046,2-(Nitromethylene)imidazolidine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3275,T3D1046,2-(Nitromethylene)imidazolidine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3276,T3D1046,2-(Nitromethylene)imidazolidine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3277,T3D1046,2-(Nitromethylene)imidazolidine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3278,T3D1046,2-(Nitromethylene)imidazolidine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3279,T3D1047,(2Z)-1-Methyl-2-(nitromethylidene)pyrrolidine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3280,T3D1047,(2Z)-1-Methyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3281,T3D1047,(2Z)-1-Methyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3282,T3D1047,(2Z)-1-Methyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3283,T3D1047,(2Z)-1-Methyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3284,T3D1048,2-Nitromethylene-azepane,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3285,T3D1048,2-Nitromethylene-azepane,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3286,T3D1048,2-Nitromethylene-azepane,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3287,T3D1048,2-Nitromethylene-azepane,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3288,T3D1048,2-Nitromethylene-azepane,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3289,T3D1049,2-Nitromethylene-piperidine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3290,T3D1049,2-Nitromethylene-piperidine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3291,T3D1049,2-Nitromethylene-piperidine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3292,T3D1049,2-Nitromethylene-piperidine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3293,T3D1049,2-Nitromethylene-piperidine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3294,T3D1050,Nitro-methylene-cyclopentane,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3295,T3D1050,Nitro-methylene-cyclopentane,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3296,T3D1050,Nitro-methylene-cyclopentane,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3297,T3D1050,Nitro-methylene-cyclopentane,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3298,T3D1050,Nitro-methylene-cyclopentane,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3299,T3D1051,"(2E)-3-Benzyl-2-(nitromethylidene)-1,3-thiazolidine",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3300,T3D1051,"(2E)-3-Benzyl-2-(nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3301,T3D1051,"(2E)-3-Benzyl-2-(nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3302,T3D1051,"(2E)-3-Benzyl-2-(nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3303,T3D1051,"(2E)-3-Benzyl-2-(nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3304,T3D1052,Nitromethylidenecyclohexane,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3305,T3D1052,Nitromethylidenecyclohexane,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3306,T3D1052,Nitromethylidenecyclohexane,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3307,T3D1052,Nitromethylidenecyclohexane,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3308,T3D1052,Nitromethylidenecyclohexane,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3309,T3D1053,"Thiazolidine, 2-(nitromethylene)",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3310,T3D1053,"Thiazolidine, 2-(nitromethylene)",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3311,T3D1053,"Thiazolidine, 2-(nitromethylene)",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3312,T3D1053,"Thiazolidine, 2-(nitromethylene)",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3313,T3D1053,"Thiazolidine, 2-(nitromethylene)",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3314,T3D1054,"(4E)-4-(Nitromethylidene)-1,2,3,5-tetrahydro-3-benzazepine",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3315,T3D1054,"(4E)-4-(Nitromethylidene)-1,2,3,5-tetrahydro-3-benzazepine",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3316,T3D1054,"(4E)-4-(Nitromethylidene)-1,2,3,5-tetrahydro-3-benzazepine",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3317,T3D1054,"(4E)-4-(Nitromethylidene)-1,2,3,5-tetrahydro-3-benzazepine",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3318,T3D1054,"(4E)-4-(Nitromethylidene)-1,2,3,5-tetrahydro-3-benzazepine",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3319,T3D1055,"(2E)-2-(Nitromethylidene)-1,3-thiazinane",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3320,T3D1055,"(2E)-2-(Nitromethylidene)-1,3-thiazinane",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3321,T3D1055,"(2E)-2-(Nitromethylidene)-1,3-thiazinane",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3322,T3D1055,"(2E)-2-(Nitromethylidene)-1,3-thiazinane",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3323,T3D1055,"(2E)-2-(Nitromethylidene)-1,3-thiazinane",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3324,T3D1056,"2-(Nitromethylidene)-1,3-thiazolidine",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3325,T3D1056,"2-(Nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3326,T3D1056,"2-(Nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3327,T3D1056,"2-(Nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3328,T3D1056,"2-(Nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3329,T3D1057,"(2Z)-2-(Nitromethylidene)-1,3-thiazolidine",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3330,T3D1057,"(2Z)-2-(Nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3331,T3D1057,"(2Z)-2-(Nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3332,T3D1057,"(2Z)-2-(Nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3333,T3D1057,"(2Z)-2-(Nitromethylidene)-1,3-thiazolidine",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3334,T3D1058,(2Z)-1-Ethyl-2-(nitromethylidene)pyrrolidine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3335,T3D1058,(2Z)-1-Ethyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3336,T3D1058,(2Z)-1-Ethyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3337,T3D1058,(2Z)-1-Ethyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3338,T3D1058,(2Z)-1-Ethyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3339,T3D1059,(2E)-2-(Nitromethylidene)-1-prop-2-enylpyrrolidine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3340,T3D1059,(2E)-2-(Nitromethylidene)-1-prop-2-enylpyrrolidine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3341,T3D1059,(2E)-2-(Nitromethylidene)-1-prop-2-enylpyrrolidine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3342,T3D1059,(2E)-2-(Nitromethylidene)-1-prop-2-enylpyrrolidine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3343,T3D1059,(2E)-2-(Nitromethylidene)-1-prop-2-enylpyrrolidine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3344,T3D1060,(2Z)-1-Benzyl-2-(nitromethylidene)pyrrolidine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3345,T3D1060,(2Z)-1-Benzyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3346,T3D1060,(2Z)-1-Benzyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3347,T3D1060,(2Z)-1-Benzyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3348,T3D1060,(2Z)-1-Benzyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3349,T3D1061,2-[(2E)-2-(Nitromethylene)hydrazino]naphthalene,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3350,T3D1061,2-[(2E)-2-(Nitromethylene)hydrazino]naphthalene,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3351,T3D1061,2-[(2E)-2-(Nitromethylene)hydrazino]naphthalene,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3352,T3D1061,2-[(2E)-2-(Nitromethylene)hydrazino]naphthalene,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3353,T3D1061,2-[(2E)-2-(Nitromethylene)hydrazino]naphthalene,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3354,T3D1062,(2E)-1-Methyl-2-(nitromethylidene)pyrrolidine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3355,T3D1062,(2E)-1-Methyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3356,T3D1062,(2E)-1-Methyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3357,T3D1062,(2E)-1-Methyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3358,T3D1062,(2E)-1-Methyl-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3359,T3D1063,2-[2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3360,T3D1063,2-[2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3361,T3D1063,2-[2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3362,T3D1063,2-[2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3363,T3D1063,2-[2-(Nitromethylidene)pyrrolidin-1-yl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3364,T3D1064,[2-(Nitromethylene)-1-pyrrolidinyl]acetonitrile,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3365,T3D1064,[2-(Nitromethylene)-1-pyrrolidinyl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3366,T3D1064,[2-(Nitromethylene)-1-pyrrolidinyl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3367,T3D1064,[2-(Nitromethylene)-1-pyrrolidinyl]acetonitrile,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3368,T3D1064,[2-(Nitromethylene)-1-pyrrolidinyl]acetonitrile,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3369,T3D1065,"1-(4,5-Dihydro-1H-imidazol-2-ylmethyl)-2,3,4,5-tetrahydro-1-benzazepine",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3370,T3D1065,"1-(4,5-Dihydro-1H-imidazol-2-ylmethyl)-2,3,4,5-tetrahydro-1-benzazepine",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3371,T3D1065,"1-(4,5-Dihydro-1H-imidazol-2-ylmethyl)-2,3,4,5-tetrahydro-1-benzazepine",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3372,T3D1065,"1-(4,5-Dihydro-1H-imidazol-2-ylmethyl)-2,3,4,5-tetrahydro-1-benzazepine",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3373,T3D1065,"1-(4,5-Dihydro-1H-imidazol-2-ylmethyl)-2,3,4,5-tetrahydro-1-benzazepine",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3374,T3D1066,"(3Z)-2-Ethyl-3-(nitromethylidene)-3a,4,5,6,7,7a-hexahydro-1H-isoindole",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3375,T3D1066,"(3Z)-2-Ethyl-3-(nitromethylidene)-3a,4,5,6,7,7a-hexahydro-1H-isoindole",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3376,T3D1066,"(3Z)-2-Ethyl-3-(nitromethylidene)-3a,4,5,6,7,7a-hexahydro-1H-isoindole",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3377,T3D1066,"(3Z)-2-Ethyl-3-(nitromethylidene)-3a,4,5,6,7,7a-hexahydro-1H-isoindole",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3378,T3D1066,"(3Z)-2-Ethyl-3-(nitromethylidene)-3a,4,5,6,7,7a-hexahydro-1H-isoindole",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3379,T3D1067,3-[(2E)-2-(Nitromethylidene)hydrazinyl]benzoic acid,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3380,T3D1067,3-[(2E)-2-(Nitromethylidene)hydrazinyl]benzoic acid,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3381,T3D1067,3-[(2E)-2-(Nitromethylidene)hydrazinyl]benzoic acid,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3382,T3D1067,3-[(2E)-2-(Nitromethylidene)hydrazinyl]benzoic acid,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3383,T3D1067,3-[(2E)-2-(Nitromethylidene)hydrazinyl]benzoic acid,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3384,T3D1068,"(2Z)-2-(Nitromethylidene)-3-phenyl-1,3-thiazolidin-4-one",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3385,T3D1068,"(2Z)-2-(Nitromethylidene)-3-phenyl-1,3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3386,T3D1068,"(2Z)-2-(Nitromethylidene)-3-phenyl-1,3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3387,T3D1068,"(2Z)-2-(Nitromethylidene)-3-phenyl-1,3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3388,T3D1068,"(2Z)-2-(Nitromethylidene)-3-phenyl-1,3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3389,T3D1069,1-(Cyclopropylmethyl)-2-(nitromethylidene)pyrrolidine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3390,T3D1069,1-(Cyclopropylmethyl)-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3391,T3D1069,1-(Cyclopropylmethyl)-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3392,T3D1069,1-(Cyclopropylmethyl)-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3393,T3D1069,1-(Cyclopropylmethyl)-2-(nitromethylidene)pyrrolidine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3394,T3D1070,3-Chloro-4-fluoro-N-[(E)-nitromethylideneamino]aniline,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3395,T3D1070,3-Chloro-4-fluoro-N-[(E)-nitromethylideneamino]aniline,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3396,T3D1070,3-Chloro-4-fluoro-N-[(E)-nitromethylideneamino]aniline,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3397,T3D1070,3-Chloro-4-fluoro-N-[(E)-nitromethylideneamino]aniline,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3398,T3D1070,3-Chloro-4-fluoro-N-[(E)-nitromethylideneamino]aniline,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3399,T3D1071,4-[(2E)-2-(Nitromethylidene)hydrazinyl]benzenesulfonamide,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3400,T3D1071,4-[(2E)-2-(Nitromethylidene)hydrazinyl]benzenesulfonamide,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3401,T3D1071,4-[(2E)-2-(Nitromethylidene)hydrazinyl]benzenesulfonamide,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3402,T3D1071,4-[(2E)-2-(Nitromethylidene)hydrazinyl]benzenesulfonamide,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3403,T3D1071,4-[(2E)-2-(Nitromethylidene)hydrazinyl]benzenesulfonamide,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3404,T3D1072,"2,3-Dimethyl-N-[(E)-nitromethylideneamino]aniline",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3405,T3D1072,"2,3-Dimethyl-N-[(E)-nitromethylideneamino]aniline",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3406,T3D1072,"2,3-Dimethyl-N-[(E)-nitromethylideneamino]aniline",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3407,T3D1072,"2,3-Dimethyl-N-[(E)-nitromethylideneamino]aniline",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3408,T3D1072,"2,3-Dimethyl-N-[(E)-nitromethylideneamino]aniline",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3409,T3D1073,(3E)-3-[Naphthalen-1-yl(nitro)methylidene]-2-benzofuran-1-one,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3410,T3D1073,(3E)-3-[Naphthalen-1-yl(nitro)methylidene]-2-benzofuran-1-one,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3411,T3D1073,(3E)-3-[Naphthalen-1-yl(nitro)methylidene]-2-benzofuran-1-one,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3412,T3D1073,(3E)-3-[Naphthalen-1-yl(nitro)methylidene]-2-benzofuran-1-one,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3413,T3D1073,(3E)-3-[Naphthalen-1-yl(nitro)methylidene]-2-benzofuran-1-one,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3414,T3D1074,(3E)-3-[(4-Chlorophenyl)-nitromethylidene]-2-benzofuran-1-one,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3415,T3D1074,(3E)-3-[(4-Chlorophenyl)-nitromethylidene]-2-benzofuran-1-one,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3416,T3D1074,(3E)-3-[(4-Chlorophenyl)-nitromethylidene]-2-benzofuran-1-one,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3417,T3D1074,(3E)-3-[(4-Chlorophenyl)-nitromethylidene]-2-benzofuran-1-one,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3418,T3D1074,(3E)-3-[(4-Chlorophenyl)-nitromethylidene]-2-benzofuran-1-one,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3419,T3D1075,"(2Z)-3-(4-Methoxyphenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3420,T3D1075,"(2Z)-3-(4-Methoxyphenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3421,T3D1075,"(2Z)-3-(4-Methoxyphenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3422,T3D1075,"(2Z)-3-(4-Methoxyphenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3423,T3D1075,"(2Z)-3-(4-Methoxyphenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3424,T3D1076,Methyl (5Z)-3-amino-5-(nitromethylidene)dithiole-4-carboxylate,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3425,T3D1076,Methyl (5Z)-3-amino-5-(nitromethylidene)dithiole-4-carboxylate,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3426,T3D1076,Methyl (5Z)-3-amino-5-(nitromethylidene)dithiole-4-carboxylate,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3427,T3D1076,Methyl (5Z)-3-amino-5-(nitromethylidene)dithiole-4-carboxylate,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3428,T3D1076,Methyl (5Z)-3-amino-5-(nitromethylidene)dithiole-4-carboxylate,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3429,T3D1077,"2,5-Bis[(2E)-2-(nitromethylidene)pyrrolidin-1-yl]benzene-1,4-diol",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3430,T3D1077,"2,5-Bis[(2E)-2-(nitromethylidene)pyrrolidin-1-yl]benzene-1,4-diol",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3431,T3D1077,"2,5-Bis[(2E)-2-(nitromethylidene)pyrrolidin-1-yl]benzene-1,4-diol",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3432,T3D1077,"2,5-Bis[(2E)-2-(nitromethylidene)pyrrolidin-1-yl]benzene-1,4-diol",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3433,T3D1077,"2,5-Bis[(2E)-2-(nitromethylidene)pyrrolidin-1-yl]benzene-1,4-diol",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3434,T3D1078,"(11E)-11-(Nitromethylidene)-[1]benzofuro[3,2-b]chromene",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3435,T3D1078,"(11E)-11-(Nitromethylidene)-[1]benzofuro[3,2-b]chromene",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3436,T3D1078,"(11E)-11-(Nitromethylidene)-[1]benzofuro[3,2-b]chromene",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3437,T3D1078,"(11E)-11-(Nitromethylidene)-[1]benzofuro[3,2-b]chromene",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3438,T3D1078,"(11E)-11-(Nitromethylidene)-[1]benzofuro[3,2-b]chromene",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3439,T3D1079,2-Chloro-5-[[2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3440,T3D1079,2-Chloro-5-[[2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3441,T3D1079,2-Chloro-5-[[2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3442,T3D1079,2-Chloro-5-[[2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3443,T3D1079,2-Chloro-5-[[2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3444,T3D1080,"N-[(E)-Nitromethylideneamino]-2-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]aniline",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3445,T3D1080,"N-[(E)-Nitromethylideneamino]-2-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]aniline",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3446,T3D1080,"N-[(E)-Nitromethylideneamino]-2-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]aniline",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3447,T3D1080,"N-[(E)-Nitromethylideneamino]-2-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]aniline",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3448,T3D1080,"N-[(E)-Nitromethylideneamino]-2-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]aniline",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3449,T3D1081,2-Chloro-5-[[(2E)-2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3450,T3D1081,2-Chloro-5-[[(2E)-2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3451,T3D1081,2-Chloro-5-[[(2E)-2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3452,T3D1081,2-Chloro-5-[[(2E)-2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3453,T3D1081,2-Chloro-5-[[(2E)-2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3454,T3D1082,(2E)-3-Methyl-2-(nitromethylidene)imidazole-1-carboximidamide,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3455,T3D1082,(2E)-3-Methyl-2-(nitromethylidene)imidazole-1-carboximidamide,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3456,T3D1082,(2E)-3-Methyl-2-(nitromethylidene)imidazole-1-carboximidamide,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3457,T3D1082,(2E)-3-Methyl-2-(nitromethylidene)imidazole-1-carboximidamide,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3458,T3D1082,(2E)-3-Methyl-2-(nitromethylidene)imidazole-1-carboximidamide,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3459,T3D1083,"(2Z)-2-(Mitromethylidene)-3-[4-(trifluoromethoxy)phenyl]-1, 3-thiazolidin-4-one",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3460,T3D1083,"(2Z)-2-(Mitromethylidene)-3-[4-(trifluoromethoxy)phenyl]-1, 3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3461,T3D1083,"(2Z)-2-(Mitromethylidene)-3-[4-(trifluoromethoxy)phenyl]-1, 3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3462,T3D1083,"(2Z)-2-(Mitromethylidene)-3-[4-(trifluoromethoxy)phenyl]-1, 3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3463,T3D1083,"(2Z)-2-(Mitromethylidene)-3-[4-(trifluoromethoxy)phenyl]-1, 3-thiazolidin-4-one",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3464,T3D1084,"1-[(6-Chloropyridin-3-yl)methyl]-2-(nitromethylidene)-1,3-diazinane",Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3465,T3D1084,"1-[(6-Chloropyridin-3-yl)methyl]-2-(nitromethylidene)-1,3-diazinane",Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3466,T3D1084,"1-[(6-Chloropyridin-3-yl)methyl]-2-(nitromethylidene)-1,3-diazinane",Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3467,T3D1084,"1-[(6-Chloropyridin-3-yl)methyl]-2-(nitromethylidene)-1,3-diazinane",Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3468,T3D1084,"1-[(6-Chloropyridin-3-yl)methyl]-2-(nitromethylidene)-1,3-diazinane",Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3469,T3D1085,(E)-N-[2-[[5-(Dimethylaminomethyl)furan-2-yl]methylsulfanyl]ethyl]-1-(4-methylpiperazin-1-yl)-2-nitroethenamine,Acetylcholine receptor subunit beta,P11230,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3470,T3D1085,(E)-N-[2-[[5-(Dimethylaminomethyl)furan-2-yl]methylsulfanyl]ethyl]-1-(4-methylpiperazin-1-yl)-2-nitroethenamine,Neuronal acetylcholine receptor subunit alpha-3,P32297,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3471,T3D1085,(E)-N-[2-[[5-(Dimethylaminomethyl)furan-2-yl]methylsulfanyl]ethyl]-1-(4-methylpiperazin-1-yl)-2-nitroethenamine,Neuronal acetylcholine receptor subunit alpha-4,P43681,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3472,T3D1085,(E)-N-[2-[[5-(Dimethylaminomethyl)furan-2-yl]methylsulfanyl]ethyl]-1-(4-methylpiperazin-1-yl)-2-nitroethenamine,Neuronal acetylcholine receptor subunit beta-2,P17787,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3473,T3D1085,(E)-N-[2-[[5-(Dimethylaminomethyl)furan-2-yl]methylsulfanyl]ethyl]-1-(4-methylpiperazin-1-yl)-2-nitroethenamine,Neuronal acetylcholine receptor subunit alpha-5,P30532,"It acts as a neurotransmitter mimic , having both excitatory and depressant Ieffects, eventually blocking postsynaptic nicotinic receptors. (R029)"
3474,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit alpha-9,Q9UGM1,Binds to nAChRs in nervous systems. (R029)
3475,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit alpha-10,Q9GZZ6,Binds to nAChRs in nervous systems. (R029)
3476,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit alpha-3,P32297,Binds to nAChRs in nervous systems. (R029)
3477,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit alpha-4,P43681,Binds to nAChRs in nervous systems. (R029)
3478,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit alpha-7,P36544,Binds to nAChRs in nervous systems. (R029)
3479,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit beta-4,P30926,Binds to nAChRs in nervous systems. (R029)
3480,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit beta-2,P17787,Binds to nAChRs in nervous systems. (R029)
3481,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit alpha-5,P30532,Binds to nAChRs in nervous systems. (R029)
3482,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit beta-3,Q05901,Binds to nAChRs in nervous systems. (R029)
3483,T3D1086,Amidochlor,Neuronal acetylcholine receptor subunit alpha-6,Q15825,Binds to nAChRs in nervous systems. (R029)
3484,T3D1087,Butachlor,Neuronal acetylcholine receptor subunit alpha-3,P32297,Binds to nAChRs in nervous systems. (R029)
3485,T3D1087,Butachlor,Neuronal acetylcholine receptor subunit alpha-4,P43681,Binds to nAChRs in nervous systems. (R029)
3486,T3D1087,Butachlor,Neuronal acetylcholine receptor subunit alpha-7,P36544,Binds to nAChRs in nervous systems. (R029)
3487,T3D1087,Butachlor,Neuronal acetylcholine receptor subunit beta-4,P30926,Binds to nAChRs in nervous systems. (R029)
3488,T3D1087,Butachlor,Neuronal acetylcholine receptor subunit beta-2,P17787,Binds to nAChRs in nervous systems. (R029)
3489,T3D1087,Butachlor,Neuronal acetylcholine receptor subunit alpha-5,P30532,Binds to nAChRs in nervous systems. (R029)
3490,T3D1087,Butachlor,Neuronal acetylcholine receptor subunit beta-3,Q05901,Binds to nAChRs in nervous systems. (R029)
3491,T3D1087,Butachlor,Neuronal acetylcholine receptor subunit alpha-6,Q15825,Binds to nAChRs in nervous systems. (R029)
3492,T3D1088,Metalaxyl,Neuronal acetylcholine receptor subunit alpha-3,P32297,Binds to nAChRs in nervous systems. (R029)
3493,T3D1088,Metalaxyl,Neuronal acetylcholine receptor subunit alpha-4,P43681,Binds to nAChRs in nervous systems. (R029)
3494,T3D1088,Metalaxyl,Neuronal acetylcholine receptor subunit alpha-7,P36544,Binds to nAChRs in nervous systems. (R029)
3495,T3D1088,Metalaxyl,Neuronal acetylcholine receptor subunit beta-4,P30926,Binds to nAChRs in nervous systems. (R029)
3496,T3D1088,Metalaxyl,Neuronal acetylcholine receptor subunit beta-2,P17787,Binds to nAChRs in nervous systems. (R029)
3497,T3D1088,Metalaxyl,Neuronal acetylcholine receptor subunit alpha-5,P30532,Binds to nAChRs in nervous systems. (R029)
3498,T3D1088,Metalaxyl,Neuronal acetylcholine receptor subunit beta-3,Q05901,Binds to nAChRs in nervous systems. (R029)
3499,T3D1088,Metalaxyl,Neuronal acetylcholine receptor subunit alpha-6,Q15825,Binds to nAChRs in nervous systems. (R029)
3500,T3D1089,Metolachlor,Neuronal acetylcholine receptor subunit alpha-3,P32297,"Metolachlor acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It also binds to nAChRs in nervous systems. (R029, S224)."
3501,T3D1089,Metolachlor,Neuronal acetylcholine receptor subunit alpha-4,P43681,"Metolachlor acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It also binds to nAChRs in nervous systems. (R029, S224)."
3502,T3D1089,Metolachlor,Neuronal acetylcholine receptor subunit alpha-7,P36544,"Metolachlor acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It also binds to nAChRs in nervous systems. (R029, S224)."
3503,T3D1089,Metolachlor,Neuronal acetylcholine receptor subunit beta-4,P30926,"Metolachlor acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It also binds to nAChRs in nervous systems. (R029, S224)."
3504,T3D1089,Metolachlor,Neuronal acetylcholine receptor subunit beta-2,P17787,"Metolachlor acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It also binds to nAChRs in nervous systems. (R029, S224)."
3505,T3D1089,Metolachlor,Neuronal acetylcholine receptor subunit alpha-5,P30532,"Metolachlor acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It also binds to nAChRs in nervous systems. (R029, S224)."
3506,T3D1089,Metolachlor,Neuronal acetylcholine receptor subunit beta-3,Q05901,"Metolachlor acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It also binds to nAChRs in nervous systems. (R029, S224)."
3507,T3D1089,Metolachlor,Neuronal acetylcholine receptor subunit alpha-6,Q15825,"Metolachlor acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It also binds to nAChRs in nervous systems. (R029, S224)."
3508,T3D1090,Propachlor,Neuronal acetylcholine receptor subunit alpha-3,P32297,"Propachlor poisoning causes an induction of microsomal hepatic UDPGT activity, which produces increased clearance of thyroid hormone, T4. Decreased levels of T4 would result in increased levels of thyroid stimulating hormone (TSH). Increased levels of TSH would result in the hyperplastic and eventually tumorigenic response of the thyroid. Propachlor metabolites also bind to nAChRs in the nervous system. (R029, S217)."
3509,T3D1090,Propachlor,Neuronal acetylcholine receptor subunit alpha-4,P43681,"Propachlor poisoning causes an induction of microsomal hepatic UDPGT activity, which produces increased clearance of thyroid hormone, T4. Decreased levels of T4 would result in increased levels of thyroid stimulating hormone (TSH). Increased levels of TSH would result in the hyperplastic and eventually tumorigenic response of the thyroid. Propachlor metabolites also bind to nAChRs in the nervous system. (R029, S217)."
3510,T3D1090,Propachlor,Neuronal acetylcholine receptor subunit alpha-7,P36544,"Propachlor poisoning causes an induction of microsomal hepatic UDPGT activity, which produces increased clearance of thyroid hormone, T4. Decreased levels of T4 would result in increased levels of thyroid stimulating hormone (TSH). Increased levels of TSH would result in the hyperplastic and eventually tumorigenic response of the thyroid. Propachlor metabolites also bind to nAChRs in the nervous system. (R029, S217)."
3511,T3D1090,Propachlor,Neuronal acetylcholine receptor subunit beta-4,P30926,"Propachlor poisoning causes an induction of microsomal hepatic UDPGT activity, which produces increased clearance of thyroid hormone, T4. Decreased levels of T4 would result in increased levels of thyroid stimulating hormone (TSH). Increased levels of TSH would result in the hyperplastic and eventually tumorigenic response of the thyroid. Propachlor metabolites also bind to nAChRs in the nervous system. (R029, S217)."
3512,T3D1090,Propachlor,Neuronal acetylcholine receptor subunit beta-2,P17787,"Propachlor poisoning causes an induction of microsomal hepatic UDPGT activity, which produces increased clearance of thyroid hormone, T4. Decreased levels of T4 would result in increased levels of thyroid stimulating hormone (TSH). Increased levels of TSH would result in the hyperplastic and eventually tumorigenic response of the thyroid. Propachlor metabolites also bind to nAChRs in the nervous system. (R029, S217)."
3513,T3D1090,Propachlor,Neuronal acetylcholine receptor subunit alpha-5,P30532,"Propachlor poisoning causes an induction of microsomal hepatic UDPGT activity, which produces increased clearance of thyroid hormone, T4. Decreased levels of T4 would result in increased levels of thyroid stimulating hormone (TSH). Increased levels of TSH would result in the hyperplastic and eventually tumorigenic response of the thyroid. Propachlor metabolites also bind to nAChRs in the nervous system. (R029, S217)."
3514,T3D1090,Propachlor,Neuronal acetylcholine receptor subunit beta-3,Q05901,"Propachlor poisoning causes an induction of microsomal hepatic UDPGT activity, which produces increased clearance of thyroid hormone, T4. Decreased levels of T4 would result in increased levels of thyroid stimulating hormone (TSH). Increased levels of TSH would result in the hyperplastic and eventually tumorigenic response of the thyroid. Propachlor metabolites also bind to nAChRs in the nervous system. (R029, S217)."
3515,T3D1090,Propachlor,Neuronal acetylcholine receptor subunit alpha-6,Q15825,"Propachlor poisoning causes an induction of microsomal hepatic UDPGT activity, which produces increased clearance of thyroid hormone, T4. Decreased levels of T4 would result in increased levels of thyroid stimulating hormone (TSH). Increased levels of TSH would result in the hyperplastic and eventually tumorigenic response of the thyroid. Propachlor metabolites also bind to nAChRs in the nervous system. (R029, S217)."
3516,T3D0390,2-Chlorobiphenyl,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3517,T3D0390,2-Chlorobiphenyl,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3518,T3D0390,2-Chlorobiphenyl,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3519,T3D0390,2-Chlorobiphenyl,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3520,T3D0390,2-Chlorobiphenyl,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3521,T3D0390,2-Chlorobiphenyl,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3522,T3D0390,2-Chlorobiphenyl,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3523,T3D0391,3-Chlorobiphenyl,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3524,T3D0391,3-Chlorobiphenyl,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3525,T3D0391,3-Chlorobiphenyl,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3526,T3D0391,3-Chlorobiphenyl,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3527,T3D0391,3-Chlorobiphenyl,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3528,T3D0391,3-Chlorobiphenyl,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3529,T3D0391,3-Chlorobiphenyl,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3530,T3D0392,4-Chlorobiphenyl,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3531,T3D0392,4-Chlorobiphenyl,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3532,T3D0392,4-Chlorobiphenyl,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3533,T3D0392,4-Chlorobiphenyl,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3534,T3D0392,4-Chlorobiphenyl,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3535,T3D0392,4-Chlorobiphenyl,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3536,T3D0392,4-Chlorobiphenyl,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3537,T3D0393,"2,2'-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3538,T3D0393,"2,2'-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3539,T3D0393,"2,2'-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3540,T3D0393,"2,2'-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3541,T3D0393,"2,2'-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3542,T3D0393,"2,2'-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3543,T3D0393,"2,2'-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3544,T3D0394,"2,3-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3545,T3D0394,"2,3-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3546,T3D0394,"2,3-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3547,T3D0394,"2,3-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3548,T3D0394,"2,3-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3549,T3D0394,"2,3-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3550,T3D0394,"2,3-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3551,T3D0395,"2,3'-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3552,T3D0395,"2,3'-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3553,T3D0395,"2,3'-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3554,T3D0395,"2,3'-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3555,T3D0395,"2,3'-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3556,T3D0395,"2,3'-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3557,T3D0395,"2,3'-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3558,T3D0396,"2,4-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3559,T3D0396,"2,4-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3560,T3D0396,"2,4-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3561,T3D0396,"2,4-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3562,T3D0396,"2,4-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3563,T3D0396,"2,4-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3564,T3D0396,"2,4-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3565,T3D0397,"2,4'-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3566,T3D0397,"2,4'-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3567,T3D0397,"2,4'-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3568,T3D0397,"2,4'-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3569,T3D0397,"2,4'-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3570,T3D0397,"2,4'-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3571,T3D0397,"2,4'-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3572,T3D0398,"2,5-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3573,T3D0398,"2,5-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3574,T3D0398,"2,5-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3575,T3D0398,"2,5-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3576,T3D0398,"2,5-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3577,T3D0398,"2,5-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3578,T3D0398,"2,5-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3579,T3D0399,"2,6-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3580,T3D0399,"2,6-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3581,T3D0399,"2,6-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3582,T3D0399,"2,6-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3583,T3D0399,"2,6-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3584,T3D0399,"2,6-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3585,T3D0399,"2,6-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3586,T3D0400,"3,3'-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3587,T3D0400,"3,3'-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3588,T3D0400,"3,3'-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3589,T3D0400,"3,3'-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3590,T3D0400,"3,3'-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3591,T3D0400,"3,3'-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3592,T3D0400,"3,3'-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3593,T3D0401,"3,4-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3594,T3D0401,"3,4-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3595,T3D0401,"3,4-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3596,T3D0401,"3,4-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3597,T3D0401,"3,4-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3598,T3D0401,"3,4-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3599,T3D0401,"3,4-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3600,T3D0402,"3,4'-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3601,T3D0402,"3,4'-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3602,T3D0402,"3,4'-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3603,T3D0402,"3,4'-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3604,T3D0402,"3,4'-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3605,T3D0402,"3,4'-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3606,T3D0402,"3,4'-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3607,T3D0403,"3,5-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3608,T3D0403,"3,5-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3609,T3D0403,"3,5-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3610,T3D0403,"3,5-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3611,T3D0403,"3,5-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3612,T3D0403,"3,5-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3613,T3D0403,"3,5-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3614,T3D0404,"4,4'-Dichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3615,T3D0404,"4,4'-Dichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3616,T3D0404,"4,4'-Dichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3617,T3D0404,"4,4'-Dichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3618,T3D0404,"4,4'-Dichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3619,T3D0404,"4,4'-Dichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3620,T3D0404,"4,4'-Dichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3621,T3D0405,"2,2',3-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3622,T3D0405,"2,2',3-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3623,T3D0405,"2,2',3-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3624,T3D0405,"2,2',3-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3625,T3D0405,"2,2',3-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3626,T3D0405,"2,2',3-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3627,T3D0405,"2,2',3-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3628,T3D0406,"2,2',4-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3629,T3D0406,"2,2',4-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3630,T3D0406,"2,2',4-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3631,T3D0406,"2,2',4-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3632,T3D0406,"2,2',4-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3633,T3D0406,"2,2',4-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3634,T3D0406,"2,2',4-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3635,T3D0407,"2,2',5-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3636,T3D0407,"2,2',5-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3637,T3D0407,"2,2',5-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3638,T3D0407,"2,2',5-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3639,T3D0407,"2,2',5-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3640,T3D0407,"2,2',5-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3641,T3D0407,"2,2',5-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3642,T3D0408,"2,2',6-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3643,T3D0408,"2,2',6-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3644,T3D0408,"2,2',6-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3645,T3D0408,"2,2',6-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3646,T3D0408,"2,2',6-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3647,T3D0408,"2,2',6-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3648,T3D0408,"2,2',6-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3649,T3D0409,"2,3,3'-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3650,T3D0409,"2,3,3'-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3651,T3D0409,"2,3,3'-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3652,T3D0409,"2,3,3'-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3653,T3D0409,"2,3,3'-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3654,T3D0409,"2,3,3'-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3655,T3D0409,"2,3,3'-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3656,T3D0410,"2,3,4-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3657,T3D0410,"2,3,4-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3658,T3D0410,"2,3,4-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3659,T3D0410,"2,3,4-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3660,T3D0410,"2,3,4-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3661,T3D0410,"2,3,4-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3662,T3D0410,"2,3,4-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3663,T3D0411,"2,3,4'-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3664,T3D0411,"2,3,4'-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3665,T3D0411,"2,3,4'-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3666,T3D0411,"2,3,4'-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3667,T3D0411,"2,3,4'-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3668,T3D0411,"2,3,4'-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3669,T3D0411,"2,3,4'-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3670,T3D0412,"2,3,5-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3671,T3D0412,"2,3,5-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3672,T3D0412,"2,3,5-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3673,T3D0412,"2,3,5-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3674,T3D0412,"2,3,5-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3675,T3D0412,"2,3,5-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3676,T3D0412,"2,3,5-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3677,T3D0413,"2,3,6-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3678,T3D0413,"2,3,6-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3679,T3D0413,"2,3,6-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3680,T3D0413,"2,3,6-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3681,T3D0413,"2,3,6-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3682,T3D0413,"2,3,6-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3683,T3D0413,"2,3,6-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3684,T3D0414,"2,3',4-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3685,T3D0414,"2,3',4-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3686,T3D0414,"2,3',4-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3687,T3D0414,"2,3',4-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3688,T3D0414,"2,3',4-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3689,T3D0414,"2,3',4-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3690,T3D0414,"2,3',4-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3691,T3D0415,"2,3',5-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3692,T3D0415,"2,3',5-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3693,T3D0415,"2,3',5-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3694,T3D0415,"2,3',5-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3695,T3D0415,"2,3',5-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3696,T3D0415,"2,3',5-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3697,T3D0415,"2,3',5-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3698,T3D0416,"2,3',6-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3699,T3D0416,"2,3',6-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3700,T3D0416,"2,3',6-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3701,T3D0416,"2,3',6-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3702,T3D0416,"2,3',6-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3703,T3D0416,"2,3',6-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3704,T3D0416,"2,3',6-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3705,T3D0417,"2,4,4'-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3706,T3D0417,"2,4,4'-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3707,T3D0417,"2,4,4'-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3708,T3D0417,"2,4,4'-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3709,T3D0417,"2,4,4'-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3710,T3D0417,"2,4,4'-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3711,T3D0417,"2,4,4'-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3712,T3D0418,"2,4,5-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3713,T3D0418,"2,4,5-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3714,T3D0418,"2,4,5-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3715,T3D0418,"2,4,5-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3716,T3D0418,"2,4,5-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3717,T3D0418,"2,4,5-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3718,T3D0418,"2,4,5-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3719,T3D0419,"2,4,6-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3720,T3D0419,"2,4,6-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3721,T3D0419,"2,4,6-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3722,T3D0419,"2,4,6-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3723,T3D0419,"2,4,6-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3724,T3D0419,"2,4,6-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3725,T3D0419,"2,4,6-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3726,T3D0420,"2,4',5-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3727,T3D0420,"2,4',5-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3728,T3D0420,"2,4',5-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3729,T3D0420,"2,4',5-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3730,T3D0420,"2,4',5-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3731,T3D0420,"2,4',5-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3732,T3D0420,"2,4',5-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3733,T3D0421,"2,4',6-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3734,T3D0421,"2,4',6-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3735,T3D0421,"2,4',6-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3736,T3D0421,"2,4',6-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3737,T3D0421,"2,4',6-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3738,T3D0421,"2,4',6-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3739,T3D0421,"2,4',6-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3740,T3D0422,"2,3',4'-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3741,T3D0422,"2,3',4'-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3742,T3D0422,"2,3',4'-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3743,T3D0422,"2,3',4'-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3744,T3D0422,"2,3',4'-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3745,T3D0422,"2,3',4'-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3746,T3D0422,"2,3',4'-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3747,T3D0423,"2,3',5'-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3748,T3D0423,"2,3',5'-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3749,T3D0423,"2,3',5'-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3750,T3D0423,"2,3',5'-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3751,T3D0423,"2,3',5'-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3752,T3D0423,"2,3',5'-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3753,T3D0423,"2,3',5'-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3754,T3D0424,"3,3',4-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3755,T3D0424,"3,3',4-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3756,T3D0424,"3,3',4-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3757,T3D0424,"3,3',4-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3758,T3D0424,"3,3',4-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3759,T3D0424,"3,3',4-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3760,T3D0424,"3,3',4-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3761,T3D0425,"3,3',5-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3762,T3D0425,"3,3',5-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3763,T3D0425,"3,3',5-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3764,T3D0425,"3,3',5-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3765,T3D0425,"3,3',5-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3766,T3D0425,"3,3',5-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3767,T3D0425,"3,3',5-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3768,T3D0426,"3,4,4'-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3769,T3D0426,"3,4,4'-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3770,T3D0426,"3,4,4'-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3771,T3D0426,"3,4,4'-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3772,T3D0426,"3,4,4'-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3773,T3D0426,"3,4,4'-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3774,T3D0426,"3,4,4'-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3775,T3D0427,"3,4,5-Tricholobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3776,T3D0427,"3,4,5-Tricholobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3777,T3D0427,"3,4,5-Tricholobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3778,T3D0427,"3,4,5-Tricholobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3779,T3D0427,"3,4,5-Tricholobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3780,T3D0427,"3,4,5-Tricholobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3781,T3D0427,"3,4,5-Tricholobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3782,T3D0428,"3,4',5-Trichlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3783,T3D0428,"3,4',5-Trichlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3784,T3D0428,"3,4',5-Trichlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3785,T3D0428,"3,4',5-Trichlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3786,T3D0428,"3,4',5-Trichlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3787,T3D0428,"3,4',5-Trichlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3788,T3D0428,"3,4',5-Trichlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3789,T3D0429,"2,2',3,3'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3790,T3D0429,"2,2',3,3'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3791,T3D0429,"2,2',3,3'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3792,T3D0429,"2,2',3,3'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3793,T3D0429,"2,2',3,3'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3794,T3D0429,"2,2',3,3'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3795,T3D0429,"2,2',3,3'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3796,T3D0430,"2,2',3,4-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3797,T3D0430,"2,2',3,4-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3798,T3D0430,"2,2',3,4-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3799,T3D0430,"2,2',3,4-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3800,T3D0430,"2,2',3,4-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3801,T3D0430,"2,2',3,4-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3802,T3D0430,"2,2',3,4-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3803,T3D0431,"2,2',3,4'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3804,T3D0431,"2,2',3,4'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3805,T3D0431,"2,2',3,4'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3806,T3D0431,"2,2',3,4'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3807,T3D0431,"2,2',3,4'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3808,T3D0431,"2,2',3,4'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3809,T3D0431,"2,2',3,4'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3810,T3D0432,"2,2',3,5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3811,T3D0432,"2,2',3,5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3812,T3D0432,"2,2',3,5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3813,T3D0432,"2,2',3,5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3814,T3D0432,"2,2',3,5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3815,T3D0432,"2,2',3,5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3816,T3D0432,"2,2',3,5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3817,T3D0433,"2,2',3,5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3818,T3D0433,"2,2',3,5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3819,T3D0433,"2,2',3,5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3820,T3D0433,"2,2',3,5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3821,T3D0433,"2,2',3,5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3822,T3D0433,"2,2',3,5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3823,T3D0433,"2,2',3,5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3824,T3D0434,"2,2',3,6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3825,T3D0434,"2,2',3,6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3826,T3D0434,"2,2',3,6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3827,T3D0434,"2,2',3,6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3828,T3D0434,"2,2',3,6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3829,T3D0434,"2,2',3,6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3830,T3D0434,"2,2',3,6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3831,T3D0435,"2,2',3,6'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3832,T3D0435,"2,2',3,6'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3833,T3D0435,"2,2',3,6'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3834,T3D0435,"2,2',3,6'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3835,T3D0435,"2,2',3,6'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3836,T3D0435,"2,2',3,6'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3837,T3D0435,"2,2',3,6'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3838,T3D0436,"2,2',4,4'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3839,T3D0436,"2,2',4,4'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3840,T3D0436,"2,2',4,4'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3841,T3D0436,"2,2',4,4'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3842,T3D0436,"2,2',4,4'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3843,T3D0436,"2,2',4,4'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3844,T3D0436,"2,2',4,4'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3845,T3D0437,"2,2',4,5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3846,T3D0437,"2,2',4,5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3847,T3D0437,"2,2',4,5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3848,T3D0437,"2,2',4,5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3849,T3D0437,"2,2',4,5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3850,T3D0437,"2,2',4,5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3851,T3D0437,"2,2',4,5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3852,T3D0438,"2,2',4,5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3853,T3D0438,"2,2',4,5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3854,T3D0438,"2,2',4,5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3855,T3D0438,"2,2',4,5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3856,T3D0438,"2,2',4,5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3857,T3D0438,"2,2',4,5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3858,T3D0438,"2,2',4,5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3859,T3D0439,"2,2',4,6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3860,T3D0439,"2,2',4,6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3861,T3D0439,"2,2',4,6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3862,T3D0439,"2,2',4,6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3863,T3D0439,"2,2',4,6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3864,T3D0439,"2,2',4,6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3865,T3D0439,"2,2',4,6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3866,T3D0440,"2,2',4,6'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3867,T3D0440,"2,2',4,6'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3868,T3D0440,"2,2',4,6'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3869,T3D0440,"2,2',4,6'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3870,T3D0440,"2,2',4,6'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3871,T3D0440,"2,2',4,6'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3872,T3D0440,"2,2',4,6'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3873,T3D0441,"2,2',5,5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3874,T3D0441,"2,2',5,5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3875,T3D0441,"2,2',5,5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3876,T3D0441,"2,2',5,5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3877,T3D0441,"2,2',5,5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3878,T3D0441,"2,2',5,5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3879,T3D0441,"2,2',5,5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3880,T3D0442,"2,2',5,6'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3881,T3D0442,"2,2',5,6'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3882,T3D0442,"2,2',5,6'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3883,T3D0442,"2,2',5,6'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3884,T3D0442,"2,2',5,6'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3885,T3D0442,"2,2',5,6'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3886,T3D0442,"2,2',5,6'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3887,T3D0443,"2,2',6,6'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3888,T3D0443,"2,2',6,6'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3889,T3D0443,"2,2',6,6'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3890,T3D0443,"2,2',6,6'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3891,T3D0443,"2,2',6,6'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3892,T3D0443,"2,2',6,6'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3893,T3D0443,"2,2',6,6'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3894,T3D0444,"2,3,3',4-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3895,T3D0444,"2,3,3',4-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3896,T3D0444,"2,3,3',4-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3897,T3D0444,"2,3,3',4-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3898,T3D0444,"2,3,3',4-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3899,T3D0444,"2,3,3',4-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3900,T3D0444,"2,3,3',4-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3901,T3D0445,"2,3,3',4'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3902,T3D0445,"2,3,3',4'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3903,T3D0445,"2,3,3',4'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3904,T3D0445,"2,3,3',4'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3905,T3D0445,"2,3,3',4'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3906,T3D0445,"2,3,3',4'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3907,T3D0445,"2,3,3',4'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3908,T3D0446,"2,3,3',5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3909,T3D0446,"2,3,3',5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3910,T3D0446,"2,3,3',5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3911,T3D0446,"2,3,3',5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3912,T3D0446,"2,3,3',5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3913,T3D0446,"2,3,3',5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3914,T3D0446,"2,3,3',5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3915,T3D0447,"2,3,3',5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3916,T3D0447,"2,3,3',5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3917,T3D0447,"2,3,3',5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3918,T3D0447,"2,3,3',5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3919,T3D0447,"2,3,3',5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3920,T3D0447,"2,3,3',5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3921,T3D0447,"2,3,3',5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3922,T3D0448,"2,3,3',6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3923,T3D0448,"2,3,3',6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3924,T3D0448,"2,3,3',6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3925,T3D0448,"2,3,3',6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3926,T3D0448,"2,3,3',6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3927,T3D0448,"2,3,3',6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3928,T3D0448,"2,3,3',6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3929,T3D0449,"2,3,4,4'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3930,T3D0449,"2,3,4,4'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3931,T3D0449,"2,3,4,4'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3932,T3D0449,"2,3,4,4'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3933,T3D0449,"2,3,4,4'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3934,T3D0449,"2,3,4,4'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3935,T3D0449,"2,3,4,4'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3936,T3D0450,"2,3,4,5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3937,T3D0450,"2,3,4,5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3938,T3D0450,"2,3,4,5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3939,T3D0450,"2,3,4,5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3940,T3D0450,"2,3,4,5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3941,T3D0450,"2,3,4,5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3942,T3D0450,"2,3,4,5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3943,T3D0451,"2,3,4,6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3944,T3D0451,"2,3,4,6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3945,T3D0451,"2,3,4,6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3946,T3D0451,"2,3,4,6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3947,T3D0451,"2,3,4,6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3948,T3D0451,"2,3,4,6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3949,T3D0451,"2,3,4,6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3950,T3D0452,"2,3,4',5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3951,T3D0452,"2,3,4',5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3952,T3D0452,"2,3,4',5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3953,T3D0452,"2,3,4',5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3954,T3D0452,"2,3,4',5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3955,T3D0452,"2,3,4',5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3956,T3D0452,"2,3,4',5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3957,T3D0453,"2,3,4',6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3958,T3D0453,"2,3,4',6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3959,T3D0453,"2,3,4',6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3960,T3D0453,"2,3,4',6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3961,T3D0453,"2,3,4',6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3962,T3D0453,"2,3,4',6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3963,T3D0453,"2,3,4',6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3964,T3D0454,"2,3,5,6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3965,T3D0454,"2,3,5,6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3966,T3D0454,"2,3,5,6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3967,T3D0454,"2,3,5,6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3968,T3D0454,"2,3,5,6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3969,T3D0454,"2,3,5,6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3970,T3D0454,"2,3,5,6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3971,T3D0455,"2,3',4,4'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3972,T3D0455,"2,3',4,4'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3973,T3D0455,"2,3',4,4'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3974,T3D0455,"2,3',4,4'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3975,T3D0455,"2,3',4,4'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3976,T3D0455,"2,3',4,4'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3977,T3D0455,"2,3',4,4'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3978,T3D0456,"2,3',4,5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3979,T3D0456,"2,3',4,5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3980,T3D0456,"2,3',4,5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3981,T3D0456,"2,3',4,5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3982,T3D0456,"2,3',4,5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3983,T3D0456,"2,3',4,5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3984,T3D0456,"2,3',4,5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3985,T3D0457,"2,3',4,5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3986,T3D0457,"2,3',4,5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3987,T3D0457,"2,3',4,5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3988,T3D0457,"2,3',4,5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3989,T3D0457,"2,3',4,5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3990,T3D0457,"2,3',4,5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3991,T3D0457,"2,3',4,5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3992,T3D0458,"2,3',4,6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
3993,T3D0458,"2,3',4,6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
3994,T3D0458,"2,3',4,6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3995,T3D0458,"2,3',4,6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
3996,T3D0458,"2,3',4,6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
3997,T3D0458,"2,3',4,6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
3998,T3D0458,"2,3',4,6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
3999,T3D0459,"2,3',4',5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4000,T3D0459,"2,3',4',5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4001,T3D0459,"2,3',4',5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4002,T3D0459,"2,3',4',5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4003,T3D0459,"2,3',4',5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4004,T3D0459,"2,3',4',5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4005,T3D0459,"2,3',4',5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4006,T3D0460,"2,3',4',6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4007,T3D0460,"2,3',4',6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4008,T3D0460,"2,3',4',6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4009,T3D0460,"2,3',4',6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4010,T3D0460,"2,3',4',6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4011,T3D0460,"2,3',4',6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4012,T3D0460,"2,3',4',6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4013,T3D0461,"2,3',5,5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4014,T3D0461,"2,3',5,5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4015,T3D0461,"2,3',5,5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4016,T3D0461,"2,3',5,5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4017,T3D0461,"2,3',5,5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4018,T3D0461,"2,3',5,5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4019,T3D0461,"2,3',5,5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4020,T3D0462,"2,3',5',6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4021,T3D0462,"2,3',5',6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4022,T3D0462,"2,3',5',6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4023,T3D0462,"2,3',5',6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4024,T3D0462,"2,3',5',6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4025,T3D0462,"2,3',5',6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4026,T3D0462,"2,3',5',6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4027,T3D0463,"2,4,4',5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4028,T3D0463,"2,4,4',5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4029,T3D0463,"2,4,4',5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4030,T3D0463,"2,4,4',5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4031,T3D0463,"2,4,4',5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4032,T3D0463,"2,4,4',5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4033,T3D0463,"2,4,4',5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4034,T3D0464,"2,4,4',6-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4035,T3D0464,"2,4,4',6-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4036,T3D0464,"2,4,4',6-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4037,T3D0464,"2,4,4',6-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4038,T3D0464,"2,4,4',6-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4039,T3D0464,"2,4,4',6-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4040,T3D0464,"2,4,4',6-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4041,T3D0465,"2,3',4',5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4042,T3D0465,"2,3',4',5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4043,T3D0465,"2,3',4',5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4044,T3D0465,"2,3',4',5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4045,T3D0465,"2,3',4',5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4046,T3D0465,"2,3',4',5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4047,T3D0465,"2,3',4',5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4048,T3D0466,"3,3',4,4'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4049,T3D0466,"3,3',4,4'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4050,T3D0466,"3,3',4,4'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4051,T3D0466,"3,3',4,4'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4052,T3D0466,"3,3',4,4'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4053,T3D0466,"3,3',4,4'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4054,T3D0466,"3,3',4,4'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4055,T3D0467,"3,3',4,5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4056,T3D0467,"3,3',4,5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4057,T3D0467,"3,3',4,5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4058,T3D0467,"3,3',4,5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4059,T3D0467,"3,3',4,5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4060,T3D0467,"3,3',4,5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4061,T3D0467,"3,3',4,5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4062,T3D0468,"3,3',4,5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4063,T3D0468,"3,3',4,5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4064,T3D0468,"3,3',4,5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4065,T3D0468,"3,3',4,5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4066,T3D0468,"3,3',4,5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4067,T3D0468,"3,3',4,5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4068,T3D0468,"3,3',4,5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4069,T3D0469,"3,3',5,5'-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4070,T3D0469,"3,3',5,5'-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4071,T3D0469,"3,3',5,5'-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4072,T3D0469,"3,3',5,5'-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4073,T3D0469,"3,3',5,5'-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4074,T3D0469,"3,3',5,5'-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4075,T3D0469,"3,3',5,5'-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4076,T3D0470,"3,4,4',5-Tetrachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4077,T3D0470,"3,4,4',5-Tetrachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4078,T3D0470,"3,4,4',5-Tetrachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4079,T3D0470,"3,4,4',5-Tetrachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4080,T3D0470,"3,4,4',5-Tetrachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4081,T3D0470,"3,4,4',5-Tetrachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4082,T3D0470,"3,4,4',5-Tetrachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4083,T3D0471,"2,2',3,3',4-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4084,T3D0471,"2,2',3,3',4-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4085,T3D0471,"2,2',3,3',4-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4086,T3D0471,"2,2',3,3',4-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4087,T3D0471,"2,2',3,3',4-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4088,T3D0471,"2,2',3,3',4-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4089,T3D0471,"2,2',3,3',4-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4090,T3D0472,"2,2',3,3',5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4091,T3D0472,"2,2',3,3',5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4092,T3D0472,"2,2',3,3',5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4093,T3D0472,"2,2',3,3',5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4094,T3D0472,"2,2',3,3',5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4095,T3D0472,"2,2',3,3',5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4096,T3D0472,"2,2',3,3',5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4097,T3D0473,"2,2',3,3',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4098,T3D0473,"2,2',3,3',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4099,T3D0473,"2,2',3,3',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4100,T3D0473,"2,2',3,3',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4101,T3D0473,"2,2',3,3',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4102,T3D0473,"2,2',3,3',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4103,T3D0473,"2,2',3,3',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4104,T3D0474,"2,2',3,4,4'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4105,T3D0474,"2,2',3,4,4'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4106,T3D0474,"2,2',3,4,4'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4107,T3D0474,"2,2',3,4,4'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4108,T3D0474,"2,2',3,4,4'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4109,T3D0474,"2,2',3,4,4'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4110,T3D0474,"2,2',3,4,4'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4111,T3D0475,"2,2',3,4,5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4112,T3D0475,"2,2',3,4,5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4113,T3D0475,"2,2',3,4,5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4114,T3D0475,"2,2',3,4,5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4115,T3D0475,"2,2',3,4,5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4116,T3D0475,"2,2',3,4,5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4117,T3D0475,"2,2',3,4,5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4118,T3D0476,"2,2',3,4,5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4119,T3D0476,"2,2',3,4,5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4120,T3D0476,"2,2',3,4,5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4121,T3D0476,"2,2',3,4,5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4122,T3D0476,"2,2',3,4,5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4123,T3D0476,"2,2',3,4,5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4124,T3D0476,"2,2',3,4,5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4125,T3D0477,"2,2',3,4,6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4126,T3D0477,"2,2',3,4,6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4127,T3D0477,"2,2',3,4,6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4128,T3D0477,"2,2',3,4,6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4129,T3D0477,"2,2',3,4,6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4130,T3D0477,"2,2',3,4,6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4131,T3D0477,"2,2',3,4,6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4132,T3D0478,"2,2',3,4,6'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4133,T3D0478,"2,2',3,4,6'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4134,T3D0478,"2,2',3,4,6'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4135,T3D0478,"2,2',3,4,6'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4136,T3D0478,"2,2',3,4,6'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4137,T3D0478,"2,2',3,4,6'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4138,T3D0478,"2,2',3,4,6'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4139,T3D0479,"2,2',3,4',5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4140,T3D0479,"2,2',3,4',5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4141,T3D0479,"2,2',3,4',5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4142,T3D0479,"2,2',3,4',5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4143,T3D0479,"2,2',3,4',5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4144,T3D0479,"2,2',3,4',5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4145,T3D0479,"2,2',3,4',5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4146,T3D0480,"2,2',3,4',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4147,T3D0480,"2,2',3,4',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4148,T3D0480,"2,2',3,4',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4149,T3D0480,"2,2',3,4',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4150,T3D0480,"2,2',3,4',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4151,T3D0480,"2,2',3,4',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4152,T3D0480,"2,2',3,4',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4153,T3D0481,"2,2',3,5,5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4154,T3D0481,"2,2',3,5,5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4155,T3D0481,"2,2',3,5,5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4156,T3D0481,"2,2',3,5,5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4157,T3D0481,"2,2',3,5,5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4158,T3D0481,"2,2',3,5,5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4159,T3D0481,"2,2',3,5,5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4160,T3D0482,"2,2',3,5,6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4161,T3D0482,"2,2',3,5,6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4162,T3D0482,"2,2',3,5,6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4163,T3D0482,"2,2',3,5,6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4164,T3D0482,"2,2',3,5,6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4165,T3D0482,"2,2',3,5,6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4166,T3D0482,"2,2',3,5,6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4167,T3D0483,"2,2',3,5,6'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4168,T3D0483,"2,2',3,5,6'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4169,T3D0483,"2,2',3,5,6'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4170,T3D0483,"2,2',3,5,6'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4171,T3D0483,"2,2',3,5,6'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4172,T3D0483,"2,2',3,5,6'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4173,T3D0483,"2,2',3,5,6'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4174,T3D0484,"2,2',3,5',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4175,T3D0484,"2,2',3,5',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4176,T3D0484,"2,2',3,5',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4177,T3D0484,"2,2',3,5',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4178,T3D0484,"2,2',3,5',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4179,T3D0484,"2,2',3,5',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4180,T3D0484,"2,2',3,5',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4181,T3D0485,"2,2',3,6,6'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4182,T3D0485,"2,2',3,6,6'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4183,T3D0485,"2,2',3,6,6'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4184,T3D0485,"2,2',3,6,6'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4185,T3D0485,"2,2',3,6,6'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4186,T3D0485,"2,2',3,6,6'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4187,T3D0485,"2,2',3,6,6'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4188,T3D0486,"2,2',3,4',5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4189,T3D0486,"2,2',3,4',5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4190,T3D0486,"2,2',3,4',5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4191,T3D0486,"2,2',3,4',5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4192,T3D0486,"2,2',3,4',5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4193,T3D0486,"2,2',3,4',5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4194,T3D0486,"2,2',3,4',5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4195,T3D0487,"2,2',3,4',6'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4196,T3D0487,"2,2',3,4',6'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4197,T3D0487,"2,2',3,4',6'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4198,T3D0487,"2,2',3,4',6'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4199,T3D0487,"2,2',3,4',6'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4200,T3D0487,"2,2',3,4',6'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4201,T3D0487,"2,2',3,4',6'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4202,T3D0488,"2,2',4,4',5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4203,T3D0488,"2,2',4,4',5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4204,T3D0488,"2,2',4,4',5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4205,T3D0488,"2,2',4,4',5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4206,T3D0488,"2,2',4,4',5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4207,T3D0488,"2,2',4,4',5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4208,T3D0488,"2,2',4,4',5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4209,T3D0489,"2,2',4,4',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4210,T3D0489,"2,2',4,4',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4211,T3D0489,"2,2',4,4',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4212,T3D0489,"2,2',4,4',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4213,T3D0489,"2,2',4,4',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4214,T3D0489,"2,2',4,4',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4215,T3D0489,"2,2',4,4',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4216,T3D0490,"2,2',4,5,5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4217,T3D0490,"2,2',4,5,5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4218,T3D0490,"2,2',4,5,5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4219,T3D0490,"2,2',4,5,5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4220,T3D0490,"2,2',4,5,5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4221,T3D0490,"2,2',4,5,5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4222,T3D0490,"2,2',4,5,5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4223,T3D0491,"2,2',4,5,6'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4224,T3D0491,"2,2',4,5,6'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4225,T3D0491,"2,2',4,5,6'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4226,T3D0491,"2,2',4,5,6'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4227,T3D0491,"2,2',4,5,6'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4228,T3D0491,"2,2',4,5,6'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4229,T3D0491,"2,2',4,5,6'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4230,T3D0492,"2,2',4,5',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4231,T3D0492,"2,2',4,5',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4232,T3D0492,"2,2',4,5',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4233,T3D0492,"2,2',4,5',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4234,T3D0492,"2,2',4,5',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4235,T3D0492,"2,2',4,5',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4236,T3D0492,"2,2',4,5',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4237,T3D0493,"2,2',4,6,6'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4238,T3D0493,"2,2',4,6,6'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4239,T3D0493,"2,2',4,6,6'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4240,T3D0493,"2,2',4,6,6'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4241,T3D0493,"2,2',4,6,6'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4242,T3D0493,"2,2',4,6,6'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4243,T3D0493,"2,2',4,6,6'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4244,T3D0494,"2,3,3',4,4'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4245,T3D0494,"2,3,3',4,4'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4246,T3D0494,"2,3,3',4,4'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4247,T3D0494,"2,3,3',4,4'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4248,T3D0494,"2,3,3',4,4'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4249,T3D0494,"2,3,3',4,4'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4250,T3D0494,"2,3,3',4,4'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4251,T3D0495,"2,3,3',4,5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4252,T3D0495,"2,3,3',4,5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4253,T3D0495,"2,3,3',4,5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4254,T3D0495,"2,3,3',4,5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4255,T3D0495,"2,3,3',4,5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4256,T3D0495,"2,3,3',4,5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4257,T3D0495,"2,3,3',4,5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4258,T3D0496,"2,3,3',4',5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4259,T3D0496,"2,3,3',4',5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4260,T3D0496,"2,3,3',4',5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4261,T3D0496,"2,3,3',4',5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4262,T3D0496,"2,3,3',4',5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4263,T3D0496,"2,3,3',4',5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4264,T3D0496,"2,3,3',4',5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4265,T3D0497,"2,3,3',4,5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4266,T3D0497,"2,3,3',4,5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4267,T3D0497,"2,3,3',4,5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4268,T3D0497,"2,3,3',4,5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4269,T3D0497,"2,3,3',4,5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4270,T3D0497,"2,3,3',4,5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4271,T3D0497,"2,3,3',4,5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4272,T3D0498,"2,3,3',4,6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4273,T3D0498,"2,3,3',4,6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4274,T3D0498,"2,3,3',4,6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4275,T3D0498,"2,3,3',4,6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4276,T3D0498,"2,3,3',4,6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4277,T3D0498,"2,3,3',4,6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4278,T3D0498,"2,3,3',4,6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4279,T3D0499,"2,3,3',4',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4280,T3D0499,"2,3,3',4',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4281,T3D0499,"2,3,3',4',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4282,T3D0499,"2,3,3',4',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4283,T3D0499,"2,3,3',4',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4284,T3D0499,"2,3,3',4',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4285,T3D0499,"2,3,3',4',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4286,T3D0500,"2,3,3',5,5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4287,T3D0500,"2,3,3',5,5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4288,T3D0500,"2,3,3',5,5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4289,T3D0500,"2,3,3',5,5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4290,T3D0500,"2,3,3',5,5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4291,T3D0500,"2,3,3',5,5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4292,T3D0500,"2,3,3',5,5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4293,T3D0501,"2,3,3',5,6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4294,T3D0501,"2,3,3',5,6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4295,T3D0501,"2,3,3',5,6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4296,T3D0501,"2,3,3',5,6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4297,T3D0501,"2,3,3',5,6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4298,T3D0501,"2,3,3',5,6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4299,T3D0501,"2,3,3',5,6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4300,T3D0502,"2,3,3',5',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4301,T3D0502,"2,3,3',5',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4302,T3D0502,"2,3,3',5',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4303,T3D0502,"2,3,3',5',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4304,T3D0502,"2,3,3',5',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4305,T3D0502,"2,3,3',5',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4306,T3D0502,"2,3,3',5',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4307,T3D0503,"2,3,4,4',5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4308,T3D0503,"2,3,4,4',5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4309,T3D0503,"2,3,4,4',5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4310,T3D0503,"2,3,4,4',5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4311,T3D0503,"2,3,4,4',5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4312,T3D0503,"2,3,4,4',5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4313,T3D0503,"2,3,4,4',5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4314,T3D0504,"2,3,4,4',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4315,T3D0504,"2,3,4,4',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4316,T3D0504,"2,3,4,4',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4317,T3D0504,"2,3,4,4',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4318,T3D0504,"2,3,4,4',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4319,T3D0504,"2,3,4,4',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4320,T3D0504,"2,3,4,4',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4321,T3D0505,"2,3,4,5,6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4322,T3D0505,"2,3,4,5,6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4323,T3D0505,"2,3,4,5,6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4324,T3D0505,"2,3,4,5,6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4325,T3D0505,"2,3,4,5,6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4326,T3D0505,"2,3,4,5,6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4327,T3D0505,"2,3,4,5,6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4328,T3D0506,"2,3,4',5,6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4329,T3D0506,"2,3,4',5,6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4330,T3D0506,"2,3,4',5,6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4331,T3D0506,"2,3,4',5,6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4332,T3D0506,"2,3,4',5,6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4333,T3D0506,"2,3,4',5,6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4334,T3D0506,"2,3,4',5,6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4335,T3D0507,"2,3',4,4',5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4336,T3D0507,"2,3',4,4',5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4337,T3D0507,"2,3',4,4',5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4338,T3D0507,"2,3',4,4',5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4339,T3D0507,"2,3',4,4',5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4340,T3D0507,"2,3',4,4',5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4341,T3D0507,"2,3',4,4',5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4342,T3D0508,"2,3',4,4',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4343,T3D0508,"2,3',4,4',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4344,T3D0508,"2,3',4,4',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4345,T3D0508,"2,3',4,4',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4346,T3D0508,"2,3',4,4',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4347,T3D0508,"2,3',4,4',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4348,T3D0508,"2,3',4,4',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4349,T3D0509,"2,3',4,5,5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4350,T3D0509,"2,3',4,5,5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4351,T3D0509,"2,3',4,5,5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4352,T3D0509,"2,3',4,5,5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4353,T3D0509,"2,3',4,5,5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4354,T3D0509,"2,3',4,5,5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4355,T3D0509,"2,3',4,5,5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4356,T3D0510,"2,3',4,5',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4357,T3D0510,"2,3',4,5',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4358,T3D0510,"2,3',4,5',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4359,T3D0510,"2,3',4,5',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4360,T3D0510,"2,3',4,5',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4361,T3D0510,"2,3',4,5',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4362,T3D0510,"2,3',4,5',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4363,T3D0511,"2,3,3',4',5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4364,T3D0511,"2,3,3',4',5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4365,T3D0511,"2,3,3',4',5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4366,T3D0511,"2,3,3',4',5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4367,T3D0511,"2,3,3',4',5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4368,T3D0511,"2,3,3',4',5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4369,T3D0511,"2,3,3',4',5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4370,T3D0512,"2,3',4,4',5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4371,T3D0512,"2,3',4,4',5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4372,T3D0512,"2,3',4,4',5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4373,T3D0512,"2,3',4,4',5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4374,T3D0512,"2,3',4,4',5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4375,T3D0512,"2,3',4,4',5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4376,T3D0512,"2,3',4,4',5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4377,T3D0513,"2,3',4',5,5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4378,T3D0513,"2,3',4',5,5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4379,T3D0513,"2,3',4',5,5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4380,T3D0513,"2,3',4',5,5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4381,T3D0513,"2,3',4',5,5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4382,T3D0513,"2,3',4',5,5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4383,T3D0513,"2,3',4',5,5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4384,T3D0514,"2,3',4',5',6-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4385,T3D0514,"2,3',4',5',6-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4386,T3D0514,"2,3',4',5',6-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4387,T3D0514,"2,3',4',5',6-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4388,T3D0514,"2,3',4',5',6-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4389,T3D0514,"2,3',4',5',6-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4390,T3D0514,"2,3',4',5',6-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4391,T3D0515,"3,3',4,4',5-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4392,T3D0515,"3,3',4,4',5-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4393,T3D0515,"3,3',4,4',5-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4394,T3D0515,"3,3',4,4',5-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4395,T3D0515,"3,3',4,4',5-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4396,T3D0515,"3,3',4,4',5-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4397,T3D0515,"3,3',4,4',5-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4398,T3D0516,"3,3',4,5,5'-Pentachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4399,T3D0516,"3,3',4,5,5'-Pentachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4400,T3D0516,"3,3',4,5,5'-Pentachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4401,T3D0516,"3,3',4,5,5'-Pentachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4402,T3D0516,"3,3',4,5,5'-Pentachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4403,T3D0516,"3,3',4,5,5'-Pentachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4404,T3D0516,"3,3',4,5,5'-Pentachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4405,T3D0517,"2,2',3,3',4,4'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4406,T3D0517,"2,2',3,3',4,4'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4407,T3D0517,"2,2',3,3',4,4'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4408,T3D0517,"2,2',3,3',4,4'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4409,T3D0517,"2,2',3,3',4,4'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4410,T3D0517,"2,2',3,3',4,4'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4411,T3D0517,"2,2',3,3',4,4'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4412,T3D0518,"2,2',3,3',4,5-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4413,T3D0518,"2,2',3,3',4,5-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4414,T3D0518,"2,2',3,3',4,5-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4415,T3D0518,"2,2',3,3',4,5-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4416,T3D0518,"2,2',3,3',4,5-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4417,T3D0518,"2,2',3,3',4,5-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4418,T3D0518,"2,2',3,3',4,5-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4419,T3D0519,"2,2',3,3',4,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4420,T3D0519,"2,2',3,3',4,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4421,T3D0519,"2,2',3,3',4,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4422,T3D0519,"2,2',3,3',4,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4423,T3D0519,"2,2',3,3',4,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4424,T3D0519,"2,2',3,3',4,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4425,T3D0519,"2,2',3,3',4,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4426,T3D0520,"2,2',3,3',4,6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4427,T3D0520,"2,2',3,3',4,6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4428,T3D0520,"2,2',3,3',4,6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4429,T3D0520,"2,2',3,3',4,6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4430,T3D0520,"2,2',3,3',4,6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4431,T3D0520,"2,2',3,3',4,6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4432,T3D0520,"2,2',3,3',4,6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4433,T3D0521,"2,2',3,3',4,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4434,T3D0521,"2,2',3,3',4,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4435,T3D0521,"2,2',3,3',4,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4436,T3D0521,"2,2',3,3',4,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4437,T3D0521,"2,2',3,3',4,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4438,T3D0521,"2,2',3,3',4,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4439,T3D0521,"2,2',3,3',4,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4440,T3D0522,"2,2',3,3',5,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4441,T3D0522,"2,2',3,3',5,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4442,T3D0522,"2,2',3,3',5,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4443,T3D0522,"2,2',3,3',5,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4444,T3D0522,"2,2',3,3',5,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4445,T3D0522,"2,2',3,3',5,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4446,T3D0522,"2,2',3,3',5,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4447,T3D0523,"2,2',3,3',5,6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4448,T3D0523,"2,2',3,3',5,6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4449,T3D0523,"2,2',3,3',5,6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4450,T3D0523,"2,2',3,3',5,6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4451,T3D0523,"2,2',3,3',5,6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4452,T3D0523,"2,2',3,3',5,6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4453,T3D0523,"2,2',3,3',5,6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4454,T3D0524,"2,2',3,3',5,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4455,T3D0524,"2,2',3,3',5,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4456,T3D0524,"2,2',3,3',5,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4457,T3D0524,"2,2',3,3',5,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4458,T3D0524,"2,2',3,3',5,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4459,T3D0524,"2,2',3,3',5,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4460,T3D0524,"2,2',3,3',5,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4461,T3D0525,"2,2',3,3',6,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4462,T3D0525,"2,2',3,3',6,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4463,T3D0525,"2,2',3,3',6,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4464,T3D0525,"2,2',3,3',6,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4465,T3D0525,"2,2',3,3',6,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4466,T3D0525,"2,2',3,3',6,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4467,T3D0525,"2,2',3,3',6,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4468,T3D0526,"2,2',3,4,4',5-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4469,T3D0526,"2,2',3,4,4',5-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4470,T3D0526,"2,2',3,4,4',5-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4471,T3D0526,"2,2',3,4,4',5-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4472,T3D0526,"2,2',3,4,4',5-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4473,T3D0526,"2,2',3,4,4',5-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4474,T3D0526,"2,2',3,4,4',5-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4475,T3D0527,"2,2',3,4,4',5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4476,T3D0527,"2,2',3,4,4',5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4477,T3D0527,"2,2',3,4,4',5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4478,T3D0527,"2,2',3,4,4',5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4479,T3D0527,"2,2',3,4,4',5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4480,T3D0527,"2,2',3,4,4',5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4481,T3D0527,"2,2',3,4,4',5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4482,T3D0528,"2,2',3,4,4',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4483,T3D0528,"2,2',3,4,4',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4484,T3D0528,"2,2',3,4,4',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4485,T3D0528,"2,2',3,4,4',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4486,T3D0528,"2,2',3,4,4',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4487,T3D0528,"2,2',3,4,4',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4488,T3D0528,"2,2',3,4,4',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4489,T3D0529,"2,2',3,4,4',6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4490,T3D0529,"2,2',3,4,4',6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4491,T3D0529,"2,2',3,4,4',6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4492,T3D0529,"2,2',3,4,4',6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4493,T3D0529,"2,2',3,4,4',6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4494,T3D0529,"2,2',3,4,4',6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4495,T3D0529,"2,2',3,4,4',6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4496,T3D0530,"2,2',3,4,5,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4497,T3D0530,"2,2',3,4,5,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4498,T3D0530,"2,2',3,4,5,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4499,T3D0530,"2,2',3,4,5,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4500,T3D0530,"2,2',3,4,5,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4501,T3D0530,"2,2',3,4,5,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4502,T3D0530,"2,2',3,4,5,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4503,T3D0531,"2,2',3,4,5,6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4504,T3D0531,"2,2',3,4,5,6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4505,T3D0531,"2,2',3,4,5,6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4506,T3D0531,"2,2',3,4,5,6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4507,T3D0531,"2,2',3,4,5,6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4508,T3D0531,"2,2',3,4,5,6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4509,T3D0531,"2,2',3,4,5,6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4510,T3D0532,"2,2',3,4,5,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4511,T3D0532,"2,2',3,4,5,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4512,T3D0532,"2,2',3,4,5,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4513,T3D0532,"2,2',3,4,5,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4514,T3D0532,"2,2',3,4,5,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4515,T3D0532,"2,2',3,4,5,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4516,T3D0532,"2,2',3,4,5,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4517,T3D0533,"2,2',3,4,5',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4518,T3D0533,"2,2',3,4,5',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4519,T3D0533,"2,2',3,4,5',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4520,T3D0533,"2,2',3,4,5',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4521,T3D0533,"2,2',3,4,5',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4522,T3D0533,"2,2',3,4,5',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4523,T3D0533,"2,2',3,4,5',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4524,T3D0534,"2,2',3,4,6,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4525,T3D0534,"2,2',3,4,6,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4526,T3D0534,"2,2',3,4,6,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4527,T3D0534,"2,2',3,4,6,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4528,T3D0534,"2,2',3,4,6,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4529,T3D0534,"2,2',3,4,6,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4530,T3D0534,"2,2',3,4,6,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4531,T3D0535,"2,2',3,4',5,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4532,T3D0535,"2,2',3,4',5,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4533,T3D0535,"2,2',3,4',5,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4534,T3D0535,"2,2',3,4',5,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4535,T3D0535,"2,2',3,4',5,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4536,T3D0535,"2,2',3,4',5,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4537,T3D0535,"2,2',3,4',5,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4538,T3D0536,"2,2',3,4',5,6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4539,T3D0536,"2,2',3,4',5,6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4540,T3D0536,"2,2',3,4',5,6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4541,T3D0536,"2,2',3,4',5,6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4542,T3D0536,"2,2',3,4',5,6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4543,T3D0536,"2,2',3,4',5,6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4544,T3D0536,"2,2',3,4',5,6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4545,T3D0537,"2,2',3,4',5,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4546,T3D0537,"2,2',3,4',5,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4547,T3D0537,"2,2',3,4',5,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4548,T3D0537,"2,2',3,4',5,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4549,T3D0537,"2,2',3,4',5,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4550,T3D0537,"2,2',3,4',5,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4551,T3D0537,"2,2',3,4',5,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4552,T3D0538,"2,2',3,4',5',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4553,T3D0538,"2,2',3,4',5',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4554,T3D0538,"2,2',3,4',5',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4555,T3D0538,"2,2',3,4',5',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4556,T3D0538,"2,2',3,4',5',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4557,T3D0538,"2,2',3,4',5',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4558,T3D0538,"2,2',3,4',5',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4559,T3D0539,"2,2',3,4',6,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4560,T3D0539,"2,2',3,4',6,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4561,T3D0539,"2,2',3,4',6,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4562,T3D0539,"2,2',3,4',6,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4563,T3D0539,"2,2',3,4',6,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4564,T3D0539,"2,2',3,4',6,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4565,T3D0539,"2,2',3,4',6,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4566,T3D0540,"2,2',3,5,5',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4567,T3D0540,"2,2',3,5,5',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4568,T3D0540,"2,2',3,5,5',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4569,T3D0540,"2,2',3,5,5',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4570,T3D0540,"2,2',3,5,5',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4571,T3D0540,"2,2',3,5,5',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4572,T3D0540,"2,2',3,5,5',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4573,T3D0541,"2,2',3,5,6,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4574,T3D0541,"2,2',3,5,6,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4575,T3D0541,"2,2',3,5,6,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4576,T3D0541,"2,2',3,5,6,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4577,T3D0541,"2,2',3,5,6,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4578,T3D0541,"2,2',3,5,6,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4579,T3D0541,"2,2',3,5,6,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4580,T3D0542,"2,2',4,4',5,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4581,T3D0542,"2,2',4,4',5,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4582,T3D0542,"2,2',4,4',5,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4583,T3D0542,"2,2',4,4',5,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4584,T3D0542,"2,2',4,4',5,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4585,T3D0542,"2,2',4,4',5,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4586,T3D0542,"2,2',4,4',5,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4587,T3D0543,"2,2',4,4',5,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4588,T3D0543,"2,2',4,4',5,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4589,T3D0543,"2,2',4,4',5,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4590,T3D0543,"2,2',4,4',5,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4591,T3D0543,"2,2',4,4',5,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4592,T3D0543,"2,2',4,4',5,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4593,T3D0543,"2,2',4,4',5,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4594,T3D0544,"2,2',4,4',6,6'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4595,T3D0544,"2,2',4,4',6,6'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4596,T3D0544,"2,2',4,4',6,6'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4597,T3D0544,"2,2',4,4',6,6'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4598,T3D0544,"2,2',4,4',6,6'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4599,T3D0544,"2,2',4,4',6,6'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4600,T3D0544,"2,2',4,4',6,6'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4601,T3D0545,"2,3,3',4,4',5-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4602,T3D0545,"2,3,3',4,4',5-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4603,T3D0545,"2,3,3',4,4',5-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4604,T3D0545,"2,3,3',4,4',5-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4605,T3D0545,"2,3,3',4,4',5-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4606,T3D0545,"2,3,3',4,4',5-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4607,T3D0545,"2,3,3',4,4',5-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4608,T3D0546,"2,3,3',4,4',5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4609,T3D0546,"2,3,3',4,4',5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4610,T3D0546,"2,3,3',4,4',5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4611,T3D0546,"2,3,3',4,4',5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4612,T3D0546,"2,3,3',4,4',5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4613,T3D0546,"2,3,3',4,4',5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4614,T3D0546,"2,3,3',4,4',5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4615,T3D0547,"2,3,3',4,4',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4616,T3D0547,"2,3,3',4,4',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4617,T3D0547,"2,3,3',4,4',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4618,T3D0547,"2,3,3',4,4',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4619,T3D0547,"2,3,3',4,4',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4620,T3D0547,"2,3,3',4,4',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4621,T3D0547,"2,3,3',4,4',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4622,T3D0548,"2,3,3',4,5,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4623,T3D0548,"2,3,3',4,5,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4624,T3D0548,"2,3,3',4,5,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4625,T3D0548,"2,3,3',4,5,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4626,T3D0548,"2,3,3',4,5,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4627,T3D0548,"2,3,3',4,5,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4628,T3D0548,"2,3,3',4,5,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4629,T3D0549,"2,3,3',4,5,6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4630,T3D0549,"2,3,3',4,5,6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4631,T3D0549,"2,3,3',4,5,6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4632,T3D0549,"2,3,3',4,5,6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4633,T3D0549,"2,3,3',4,5,6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4634,T3D0549,"2,3,3',4,5,6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4635,T3D0549,"2,3,3',4,5,6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4636,T3D0550,"2,3,3',4,5',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4637,T3D0550,"2,3,3',4,5',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4638,T3D0550,"2,3,3',4,5',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4639,T3D0550,"2,3,3',4,5',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4640,T3D0550,"2,3,3',4,5',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4641,T3D0550,"2,3,3',4,5',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4642,T3D0550,"2,3,3',4,5',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4643,T3D0551,"2,3,3',4',5,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4644,T3D0551,"2,3,3',4',5,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4645,T3D0551,"2,3,3',4',5,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4646,T3D0551,"2,3,3',4',5,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4647,T3D0551,"2,3,3',4',5,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4648,T3D0551,"2,3,3',4',5,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4649,T3D0551,"2,3,3',4',5,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4650,T3D0552,"2,3,3',4',5,6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4651,T3D0552,"2,3,3',4',5,6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4652,T3D0552,"2,3,3',4',5,6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4653,T3D0552,"2,3,3',4',5,6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4654,T3D0552,"2,3,3',4',5,6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4655,T3D0552,"2,3,3',4',5,6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4656,T3D0552,"2,3,3',4',5,6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4657,T3D0553,"2,3,3',4',5',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4658,T3D0553,"2,3,3',4',5',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4659,T3D0553,"2,3,3',4',5',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4660,T3D0553,"2,3,3',4',5',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4661,T3D0553,"2,3,3',4',5',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4662,T3D0553,"2,3,3',4',5',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4663,T3D0553,"2,3,3',4',5',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4664,T3D0554,"2,3,3',5,5',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4665,T3D0554,"2,3,3',5,5',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4666,T3D0554,"2,3,3',5,5',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4667,T3D0554,"2,3,3',5,5',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4668,T3D0554,"2,3,3',5,5',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4669,T3D0554,"2,3,3',5,5',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4670,T3D0554,"2,3,3',5,5',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4671,T3D0555,"2,3,4,4',5,6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4672,T3D0555,"2,3,4,4',5,6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4673,T3D0555,"2,3,4,4',5,6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4674,T3D0555,"2,3,4,4',5,6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4675,T3D0555,"2,3,4,4',5,6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4676,T3D0555,"2,3,4,4',5,6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4677,T3D0555,"2,3,4,4',5,6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4678,T3D0556,"2,3',4,4',5,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4679,T3D0556,"2,3',4,4',5,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4680,T3D0556,"2,3',4,4',5,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4681,T3D0556,"2,3',4,4',5,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4682,T3D0556,"2,3',4,4',5,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4683,T3D0556,"2,3',4,4',5,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4684,T3D0556,"2,3',4,4',5,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4685,T3D0557,"2,3',4,4',5',6-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4686,T3D0557,"2,3',4,4',5',6-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4687,T3D0557,"2,3',4,4',5',6-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4688,T3D0557,"2,3',4,4',5',6-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4689,T3D0557,"2,3',4,4',5',6-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4690,T3D0557,"2,3',4,4',5',6-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4691,T3D0557,"2,3',4,4',5',6-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4692,T3D0558,"3,3',4,4',5,5'-Hexachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4693,T3D0558,"3,3',4,4',5,5'-Hexachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4694,T3D0558,"3,3',4,4',5,5'-Hexachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4695,T3D0558,"3,3',4,4',5,5'-Hexachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4696,T3D0558,"3,3',4,4',5,5'-Hexachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4697,T3D0558,"3,3',4,4',5,5'-Hexachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4698,T3D0558,"3,3',4,4',5,5'-Hexachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4699,T3D0559,"2,2',3,3',4,4',5-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4700,T3D0559,"2,2',3,3',4,4',5-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4701,T3D0559,"2,2',3,3',4,4',5-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4702,T3D0559,"2,2',3,3',4,4',5-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4703,T3D0559,"2,2',3,3',4,4',5-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4704,T3D0559,"2,2',3,3',4,4',5-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4705,T3D0559,"2,2',3,3',4,4',5-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4706,T3D0560,"2,2',3,3',4,4',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4707,T3D0560,"2,2',3,3',4,4',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4708,T3D0560,"2,2',3,3',4,4',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4709,T3D0560,"2,2',3,3',4,4',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4710,T3D0560,"2,2',3,3',4,4',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4711,T3D0560,"2,2',3,3',4,4',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4712,T3D0560,"2,2',3,3',4,4',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4713,T3D0561,"2,2',3,3',4,5,5'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4714,T3D0561,"2,2',3,3',4,5,5'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4715,T3D0561,"2,2',3,3',4,5,5'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4716,T3D0561,"2,2',3,3',4,5,5'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4717,T3D0561,"2,2',3,3',4,5,5'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4718,T3D0561,"2,2',3,3',4,5,5'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4719,T3D0561,"2,2',3,3',4,5,5'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4720,T3D0562,"2,2',3,3',4,5,6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4721,T3D0562,"2,2',3,3',4,5,6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4722,T3D0562,"2,2',3,3',4,5,6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4723,T3D0562,"2,2',3,3',4,5,6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4724,T3D0562,"2,2',3,3',4,5,6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4725,T3D0562,"2,2',3,3',4,5,6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4726,T3D0562,"2,2',3,3',4,5,6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4727,T3D0563,"2,2',3,3',4,5,6'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4728,T3D0563,"2,2',3,3',4,5,6'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4729,T3D0563,"2,2',3,3',4,5,6'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4730,T3D0563,"2,2',3,3',4,5,6'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4731,T3D0563,"2,2',3,3',4,5,6'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4732,T3D0563,"2,2',3,3',4,5,6'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4733,T3D0563,"2,2',3,3',4,5,6'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4734,T3D0564,"2,2',3,3',4,5',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4735,T3D0564,"2,2',3,3',4,5',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4736,T3D0564,"2,2',3,3',4,5',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4737,T3D0564,"2,2',3,3',4,5',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4738,T3D0564,"2,2',3,3',4,5',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4739,T3D0564,"2,2',3,3',4,5',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4740,T3D0564,"2,2',3,3',4,5',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4741,T3D0565,"2,2',3,3',4,6,6'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4742,T3D0565,"2,2',3,3',4,6,6'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4743,T3D0565,"2,2',3,3',4,6,6'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4744,T3D0565,"2,2',3,3',4,6,6'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4745,T3D0565,"2,2',3,3',4,6,6'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4746,T3D0565,"2,2',3,3',4,6,6'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4747,T3D0565,"2,2',3,3',4,6,6'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4748,T3D0566,"2,2',3,3',4,5',6'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4749,T3D0566,"2,2',3,3',4,5',6'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4750,T3D0566,"2,2',3,3',4,5',6'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4751,T3D0566,"2,2',3,3',4,5',6'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4752,T3D0566,"2,2',3,3',4,5',6'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4753,T3D0566,"2,2',3,3',4,5',6'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4754,T3D0566,"2,2',3,3',4,5',6'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4755,T3D0567,"2,2',3,3',5,5',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4756,T3D0567,"2,2',3,3',5,5',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4757,T3D0567,"2,2',3,3',5,5',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4758,T3D0567,"2,2',3,3',5,5',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4759,T3D0567,"2,2',3,3',5,5',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4760,T3D0567,"2,2',3,3',5,5',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4761,T3D0567,"2,2',3,3',5,5',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4762,T3D0568,"2,2',3,3',5,6,6'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4763,T3D0568,"2,2',3,3',5,6,6'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4764,T3D0568,"2,2',3,3',5,6,6'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4765,T3D0568,"2,2',3,3',5,6,6'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4766,T3D0568,"2,2',3,3',5,6,6'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4767,T3D0568,"2,2',3,3',5,6,6'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4768,T3D0568,"2,2',3,3',5,6,6'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4769,T3D0569,"2,2',3,4,4',5,5'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4770,T3D0569,"2,2',3,4,4',5,5'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4771,T3D0569,"2,2',3,4,4',5,5'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4772,T3D0569,"2,2',3,4,4',5,5'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4773,T3D0569,"2,2',3,4,4',5,5'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4774,T3D0569,"2,2',3,4,4',5,5'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4775,T3D0569,"2,2',3,4,4',5,5'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4776,T3D0570,"2,2',3,4,4',5,6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4777,T3D0570,"2,2',3,4,4',5,6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4778,T3D0570,"2,2',3,4,4',5,6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4779,T3D0570,"2,2',3,4,4',5,6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4780,T3D0570,"2,2',3,4,4',5,6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4781,T3D0570,"2,2',3,4,4',5,6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4782,T3D0570,"2,2',3,4,4',5,6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4783,T3D0571,"2,2',3,4,4',5,6'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4784,T3D0571,"2,2',3,4,4',5,6'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4785,T3D0571,"2,2',3,4,4',5,6'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4786,T3D0571,"2,2',3,4,4',5,6'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4787,T3D0571,"2,2',3,4,4',5,6'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4788,T3D0571,"2,2',3,4,4',5,6'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4789,T3D0571,"2,2',3,4,4',5,6'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4790,T3D0572,"2,2',3,4,4',5',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4791,T3D0572,"2,2',3,4,4',5',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4792,T3D0572,"2,2',3,4,4',5',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4793,T3D0572,"2,2',3,4,4',5',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4794,T3D0572,"2,2',3,4,4',5',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4795,T3D0572,"2,2',3,4,4',5',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4796,T3D0572,"2,2',3,4,4',5',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4797,T3D0573,"2,2',3,4,4',6,6'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4798,T3D0573,"2,2',3,4,4',6,6'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4799,T3D0573,"2,2',3,4,4',6,6'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4800,T3D0573,"2,2',3,4,4',6,6'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4801,T3D0573,"2,2',3,4,4',6,6'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4802,T3D0573,"2,2',3,4,4',6,6'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4803,T3D0573,"2,2',3,4,4',6,6'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4804,T3D0574,"2,2',3,4,5,5',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4805,T3D0574,"2,2',3,4,5,5',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4806,T3D0574,"2,2',3,4,5,5',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4807,T3D0574,"2,2',3,4,5,5',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4808,T3D0574,"2,2',3,4,5,5',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4809,T3D0574,"2,2',3,4,5,5',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4810,T3D0574,"2,2',3,4,5,5',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4811,T3D0575,"2,2',3,4,5,6,6'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4812,T3D0575,"2,2',3,4,5,6,6'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4813,T3D0575,"2,2',3,4,5,6,6'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4814,T3D0575,"2,2',3,4,5,6,6'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4815,T3D0575,"2,2',3,4,5,6,6'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4816,T3D0575,"2,2',3,4,5,6,6'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4817,T3D0575,"2,2',3,4,5,6,6'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4818,T3D0576,"2,2',3,4',5,5',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4819,T3D0576,"2,2',3,4',5,5',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4820,T3D0576,"2,2',3,4',5,5',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4821,T3D0576,"2,2',3,4',5,5',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4822,T3D0576,"2,2',3,4',5,5',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4823,T3D0576,"2,2',3,4',5,5',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4824,T3D0576,"2,2',3,4',5,5',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4825,T3D0577,"2,2',3,4',5,6,6'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4826,T3D0577,"2,2',3,4',5,6,6'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4827,T3D0577,"2,2',3,4',5,6,6'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4828,T3D0577,"2,2',3,4',5,6,6'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4829,T3D0577,"2,2',3,4',5,6,6'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4830,T3D0577,"2,2',3,4',5,6,6'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4831,T3D0577,"2,2',3,4',5,6,6'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4832,T3D0578,"2,3,3',4,4',5,5'-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4833,T3D0578,"2,3,3',4,4',5,5'-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4834,T3D0578,"2,3,3',4,4',5,5'-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4835,T3D0578,"2,3,3',4,4',5,5'-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4836,T3D0578,"2,3,3',4,4',5,5'-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4837,T3D0578,"2,3,3',4,4',5,5'-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4838,T3D0578,"2,3,3',4,4',5,5'-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4839,T3D0579,"2,3,3',4,4',5,6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4840,T3D0579,"2,3,3',4,4',5,6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4841,T3D0579,"2,3,3',4,4',5,6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4842,T3D0579,"2,3,3',4,4',5,6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4843,T3D0579,"2,3,3',4,4',5,6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4844,T3D0579,"2,3,3',4,4',5,6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4845,T3D0579,"2,3,3',4,4',5,6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4846,T3D0580,"2,3,3',4,4',5',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4847,T3D0580,"2,3,3',4,4',5',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4848,T3D0580,"2,3,3',4,4',5',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4849,T3D0580,"2,3,3',4,4',5',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4850,T3D0580,"2,3,3',4,4',5',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4851,T3D0580,"2,3,3',4,4',5',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4852,T3D0580,"2,3,3',4,4',5',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4853,T3D0581,"2,3,3',4,5,5',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4854,T3D0581,"2,3,3',4,5,5',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4855,T3D0581,"2,3,3',4,5,5',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4856,T3D0581,"2,3,3',4,5,5',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4857,T3D0581,"2,3,3',4,5,5',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4858,T3D0581,"2,3,3',4,5,5',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4859,T3D0581,"2,3,3',4,5,5',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4860,T3D0582,"2,3,3',4',5,5',6-Heptachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4861,T3D0582,"2,3,3',4',5,5',6-Heptachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4862,T3D0582,"2,3,3',4',5,5',6-Heptachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4863,T3D0582,"2,3,3',4',5,5',6-Heptachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4864,T3D0582,"2,3,3',4',5,5',6-Heptachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4865,T3D0582,"2,3,3',4',5,5',6-Heptachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4866,T3D0582,"2,3,3',4',5,5',6-Heptachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4867,T3D0583,"2,2',3,3',4,4',5,5'-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4868,T3D0583,"2,2',3,3',4,4',5,5'-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4869,T3D0583,"2,2',3,3',4,4',5,5'-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4870,T3D0583,"2,2',3,3',4,4',5,5'-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4871,T3D0583,"2,2',3,3',4,4',5,5'-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4872,T3D0583,"2,2',3,3',4,4',5,5'-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4873,T3D0583,"2,2',3,3',4,4',5,5'-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4874,T3D0584,"2,2',3,3',4,4',5,6-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4875,T3D0584,"2,2',3,3',4,4',5,6-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4876,T3D0584,"2,2',3,3',4,4',5,6-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4877,T3D0584,"2,2',3,3',4,4',5,6-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4878,T3D0584,"2,2',3,3',4,4',5,6-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4879,T3D0584,"2,2',3,3',4,4',5,6-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4880,T3D0584,"2,2',3,3',4,4',5,6-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4881,T3D0585,"2,2',3,3',4,4',5,6'-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4882,T3D0585,"2,2',3,3',4,4',5,6'-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4883,T3D0585,"2,2',3,3',4,4',5,6'-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4884,T3D0585,"2,2',3,3',4,4',5,6'-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4885,T3D0585,"2,2',3,3',4,4',5,6'-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4886,T3D0585,"2,2',3,3',4,4',5,6'-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4887,T3D0585,"2,2',3,3',4,4',5,6'-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4888,T3D0586,"2,2',3,3',4,4',6,6'-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4889,T3D0586,"2,2',3,3',4,4',6,6'-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4890,T3D0586,"2,2',3,3',4,4',6,6'-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4891,T3D0586,"2,2',3,3',4,4',6,6'-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4892,T3D0586,"2,2',3,3',4,4',6,6'-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4893,T3D0586,"2,2',3,3',4,4',6,6'-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4894,T3D0586,"2,2',3,3',4,4',6,6'-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4895,T3D0587,"2,2',3,3',4,5,5',6-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4896,T3D0587,"2,2',3,3',4,5,5',6-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4897,T3D0587,"2,2',3,3',4,5,5',6-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4898,T3D0587,"2,2',3,3',4,5,5',6-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4899,T3D0587,"2,2',3,3',4,5,5',6-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4900,T3D0587,"2,2',3,3',4,5,5',6-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4901,T3D0587,"2,2',3,3',4,5,5',6-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4902,T3D0588,"2,2',3,3',4,5,5',6'-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4903,T3D0588,"2,2',3,3',4,5,5',6'-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4904,T3D0588,"2,2',3,3',4,5,5',6'-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4905,T3D0588,"2,2',3,3',4,5,5',6'-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4906,T3D0588,"2,2',3,3',4,5,5',6'-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4907,T3D0588,"2,2',3,3',4,5,5',6'-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4908,T3D0588,"2,2',3,3',4,5,5',6'-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4909,T3D0589,"2,2',3,3',4,5,6,6'-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4910,T3D0589,"2,2',3,3',4,5,6,6'-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4911,T3D0589,"2,2',3,3',4,5,6,6'-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4912,T3D0589,"2,2',3,3',4,5,6,6'-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4913,T3D0589,"2,2',3,3',4,5,6,6'-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4914,T3D0589,"2,2',3,3',4,5,6,6'-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4915,T3D0589,"2,2',3,3',4,5,6,6'-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4916,T3D0590,"2,2',3,3',4,5',6,6'-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4917,T3D0590,"2,2',3,3',4,5',6,6'-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4918,T3D0590,"2,2',3,3',4,5',6,6'-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4919,T3D0590,"2,2',3,3',4,5',6,6'-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4920,T3D0590,"2,2',3,3',4,5',6,6'-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4921,T3D0590,"2,2',3,3',4,5',6,6'-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4922,T3D0590,"2,2',3,3',4,5',6,6'-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4923,T3D0591,"2,2',3,3',5,5',6,6'-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4924,T3D0591,"2,2',3,3',5,5',6,6'-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4925,T3D0591,"2,2',3,3',5,5',6,6'-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4926,T3D0591,"2,2',3,3',5,5',6,6'-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4927,T3D0591,"2,2',3,3',5,5',6,6'-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4928,T3D0591,"2,2',3,3',5,5',6,6'-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4929,T3D0591,"2,2',3,3',5,5',6,6'-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4930,T3D0592,"2,2',3,4,4',5,5',6-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4931,T3D0592,"2,2',3,4,4',5,5',6-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4932,T3D0592,"2,2',3,4,4',5,5',6-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4933,T3D0592,"2,2',3,4,4',5,5',6-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4934,T3D0592,"2,2',3,4,4',5,5',6-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4935,T3D0592,"2,2',3,4,4',5,5',6-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4936,T3D0592,"2,2',3,4,4',5,5',6-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4937,T3D0593,"2,2',3,4,4',5,6,6'-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4938,T3D0593,"2,2',3,4,4',5,6,6'-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4939,T3D0593,"2,2',3,4,4',5,6,6'-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4940,T3D0593,"2,2',3,4,4',5,6,6'-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4941,T3D0593,"2,2',3,4,4',5,6,6'-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4942,T3D0593,"2,2',3,4,4',5,6,6'-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4943,T3D0593,"2,2',3,4,4',5,6,6'-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4944,T3D0594,"2,3,3',4,4',5,5',6-Octachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4945,T3D0594,"2,3,3',4,4',5,5',6-Octachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4946,T3D0594,"2,3,3',4,4',5,5',6-Octachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4947,T3D0594,"2,3,3',4,4',5,5',6-Octachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4948,T3D0594,"2,3,3',4,4',5,5',6-Octachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4949,T3D0594,"2,3,3',4,4',5,5',6-Octachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4950,T3D0594,"2,3,3',4,4',5,5',6-Octachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4951,T3D0595,"2,2',3,3',4,4',5,5',6-Nonachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4952,T3D0595,"2,2',3,3',4,4',5,5',6-Nonachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4953,T3D0595,"2,2',3,3',4,4',5,5',6-Nonachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4954,T3D0595,"2,2',3,3',4,4',5,5',6-Nonachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4955,T3D0595,"2,2',3,3',4,4',5,5',6-Nonachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4956,T3D0595,"2,2',3,3',4,4',5,5',6-Nonachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4957,T3D0595,"2,2',3,3',4,4',5,5',6-Nonachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4958,T3D0596,"2,2',3,3',4,4',5,6,6'-Nonachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4959,T3D0596,"2,2',3,3',4,4',5,6,6'-Nonachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4960,T3D0596,"2,2',3,3',4,4',5,6,6'-Nonachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4961,T3D0596,"2,2',3,3',4,4',5,6,6'-Nonachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4962,T3D0596,"2,2',3,3',4,4',5,6,6'-Nonachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4963,T3D0596,"2,2',3,3',4,4',5,6,6'-Nonachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4964,T3D0596,"2,2',3,3',4,4',5,6,6'-Nonachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4965,T3D0597,"2,2',3,3',4,5,5',6,6'-Nonachlorobiphenyl",Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4966,T3D0597,"2,2',3,3',4,5,5',6,6'-Nonachlorobiphenyl",Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4967,T3D0597,"2,2',3,3',4,5,5',6,6'-Nonachlorobiphenyl",Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4968,T3D0597,"2,2',3,3',4,5,5',6,6'-Nonachlorobiphenyl",Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4969,T3D0597,"2,2',3,3',4,5,5',6,6'-Nonachlorobiphenyl",Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4970,T3D0597,"2,2',3,3',4,5,5',6,6'-Nonachlorobiphenyl",Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4971,T3D0597,"2,2',3,3',4,5,5',6,6'-Nonachlorobiphenyl",Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4972,T3D0598,Decachlorobiphenyl,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4973,T3D0598,Decachlorobiphenyl,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4974,T3D0598,Decachlorobiphenyl,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4975,T3D0598,Decachlorobiphenyl,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4976,T3D0598,Decachlorobiphenyl,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4977,T3D0598,Decachlorobiphenyl,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4978,T3D0598,Decachlorobiphenyl,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4979,T3D0601,Aroclor 1210,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4980,T3D0601,Aroclor 1210,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4981,T3D0601,Aroclor 1210,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4982,T3D0601,Aroclor 1210,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4983,T3D0601,Aroclor 1210,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4984,T3D0601,Aroclor 1210,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4985,T3D0601,Aroclor 1210,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4986,T3D0602,Aroclor 1216,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4987,T3D0602,Aroclor 1216,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4988,T3D0602,Aroclor 1216,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4989,T3D0602,Aroclor 1216,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4990,T3D0602,Aroclor 1216,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4991,T3D0602,Aroclor 1216,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4992,T3D0602,Aroclor 1216,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
4993,T3D0604,Aroclor 1231,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
4994,T3D0604,Aroclor 1231,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
4995,T3D0604,Aroclor 1231,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4996,T3D0604,Aroclor 1231,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
4997,T3D0604,Aroclor 1231,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
4998,T3D0604,Aroclor 1231,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
4999,T3D0604,Aroclor 1231,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
5000,T3D0609,Aroclor 1250,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
5001,T3D0609,Aroclor 1250,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
5002,T3D0609,Aroclor 1250,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
5003,T3D0609,Aroclor 1250,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
5004,T3D0609,Aroclor 1250,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
5005,T3D0609,Aroclor 1250,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
5006,T3D0609,Aroclor 1250,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
5007,T3D0610,Aroclor 1252,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
5008,T3D0610,Aroclor 1252,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
5009,T3D0610,Aroclor 1252,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
5010,T3D0610,Aroclor 1252,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
5011,T3D0610,Aroclor 1252,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
5012,T3D0610,Aroclor 1252,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
5013,T3D0610,Aroclor 1252,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
5014,T3D0613,Aroclor 1262,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
5015,T3D0613,Aroclor 1262,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
5016,T3D0613,Aroclor 1262,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
5017,T3D0613,Aroclor 1262,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
5018,T3D0613,Aroclor 1262,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
5019,T3D0613,Aroclor 1262,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
5020,T3D0613,Aroclor 1262,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
5021,T3D0614,Aroclor 1268,Aromatic-L-amino-acid decarboxylase,P20711,PCB inhibition of aromatic-L-amino-acid decarboxylase is believed to cause decreased dopamine synthesis. (R012)
5022,T3D0614,Aroclor 1268,Aryl hydrocarbon receptor,P35869,"Dioxin-like PCBs bind to the aryl hydrocarbon receptor, which disrupts cell function by altering the transcription of genes, mainly be inducing the expression of hepatic Phase I and Phase II enzymes, especially of the cytochrome P450 family. (R015)"
5023,T3D0614,Aroclor 1268,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
5024,T3D0614,Aroclor 1268,Estrogen receptor beta,Q92731,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
5025,T3D0614,Aroclor 1268,Estrogen sulfotransferase,P49888,"PCBs can cause endocrine disurption by binding to estrogen sulfotransferase, which can stimulate the growth of certain cancer cells and produce other estrogenic effects, such as reproductive dysfunction. (R013, R203)"
5026,T3D0614,Aroclor 1268,Tyrosine 3-monooxygenase,P07101,PCB inhibition of tyrosine 3-monooxygenase is believed to cause decreased dopamine synthesis. (R012)
5027,T3D0614,Aroclor 1268,Uteroglobin,P11684,PCBs will bioaccumulate by binding to receptor proteins such as uteroglobin. (R071)
5028,T3D0275,Adamsite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5029,T3D0275,Adamsite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5030,T3D0275,Adamsite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5031,T3D0275,Adamsite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5032,T3D0275,Adamsite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5033,T3D0275,Adamsite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5034,T3D0275,Adamsite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5035,T3D0275,Adamsite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5036,T3D0275,Adamsite,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5037,T3D0275,Adamsite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5038,T3D0275,Adamsite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5039,T3D0275,Adamsite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5040,T3D0275,Adamsite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5041,T3D0275,Adamsite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5042,T3D0275,Adamsite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
5043,T3D0275,Adamsite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
5044,T3D0275,Adamsite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5045,T3D0275,Adamsite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5046,T3D0275,Adamsite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5047,T3D0275,Adamsite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5048,T3D0275,Adamsite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5049,T3D0275,Adamsite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5050,T3D0275,Adamsite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5051,T3D0275,Adamsite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5052,T3D0275,Adamsite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5053,T3D0275,Adamsite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5054,T3D0275,Adamsite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5055,T3D0275,Adamsite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5056,T3D0275,Adamsite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5057,T3D0275,Adamsite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5058,T3D0275,Adamsite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5059,T3D0275,Adamsite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5060,T3D0275,Adamsite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5061,T3D0275,Adamsite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5062,T3D0275,Adamsite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5063,T3D0275,Adamsite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5064,T3D0275,Adamsite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5065,T3D0275,Adamsite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5066,T3D0275,Adamsite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5067,T3D0275,Adamsite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5068,T3D0275,Adamsite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5069,T3D0275,Adamsite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5070,T3D0275,Adamsite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5071,T3D0275,Adamsite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5072,T3D0276,Arsenic trisulfide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5073,T3D0276,Arsenic trisulfide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5074,T3D0276,Arsenic trisulfide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5075,T3D0276,Arsenic trisulfide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5076,T3D0276,Arsenic trisulfide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5077,T3D0276,Arsenic trisulfide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5078,T3D0276,Arsenic trisulfide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5079,T3D0276,Arsenic trisulfide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5080,T3D0276,Arsenic trisulfide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5081,T3D0276,Arsenic trisulfide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5082,T3D0276,Arsenic trisulfide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5083,T3D0276,Arsenic trisulfide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5084,T3D0276,Arsenic trisulfide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5085,T3D0276,Arsenic trisulfide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5086,T3D0276,Arsenic trisulfide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5087,T3D0276,Arsenic trisulfide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5088,T3D0276,Arsenic trisulfide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5089,T3D0277,Arsenic disulfide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5090,T3D0277,Arsenic disulfide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5091,T3D0277,Arsenic disulfide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5092,T3D0277,Arsenic disulfide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5093,T3D0277,Arsenic disulfide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5094,T3D0277,Arsenic disulfide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5095,T3D0277,Arsenic disulfide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5096,T3D0277,Arsenic disulfide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5097,T3D0277,Arsenic disulfide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5098,T3D0277,Arsenic disulfide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5099,T3D0277,Arsenic disulfide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5100,T3D0277,Arsenic disulfide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5101,T3D0277,Arsenic disulfide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5102,T3D0277,Arsenic disulfide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5103,T3D0277,Arsenic disulfide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5104,T3D0277,Arsenic disulfide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5105,T3D0277,Arsenic disulfide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5106,T3D0278,Arsenic pentasulfide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5107,T3D0278,Arsenic pentasulfide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5108,T3D0278,Arsenic pentasulfide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5109,T3D0278,Arsenic pentasulfide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5110,T3D0278,Arsenic pentasulfide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5111,T3D0278,Arsenic pentasulfide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5112,T3D0278,Arsenic pentasulfide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5113,T3D0278,Arsenic pentasulfide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5114,T3D0278,Arsenic pentasulfide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5115,T3D0278,Arsenic pentasulfide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5116,T3D0278,Arsenic pentasulfide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5117,T3D0278,Arsenic pentasulfide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5118,T3D0278,Arsenic pentasulfide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5119,T3D0278,Arsenic pentasulfide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5120,T3D0278,Arsenic pentasulfide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5121,T3D0278,Arsenic pentasulfide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5122,T3D0278,Arsenic pentasulfide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5123,T3D0278,Arsenic pentasulfide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5124,T3D0279,Arsenic trichloride,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5125,T3D0279,Arsenic trichloride,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5126,T3D0279,Arsenic trichloride,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5127,T3D0279,Arsenic trichloride,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5128,T3D0279,Arsenic trichloride,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5129,T3D0279,Arsenic trichloride,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5130,T3D0279,Arsenic trichloride,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5131,T3D0279,Arsenic trichloride,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5132,T3D0279,Arsenic trichloride,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5133,T3D0279,Arsenic trichloride,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5134,T3D0279,Arsenic trichloride,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5135,T3D0279,Arsenic trichloride,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5136,T3D0279,Arsenic trichloride,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5137,T3D0279,Arsenic trichloride,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5138,T3D0279,Arsenic trichloride,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5139,T3D0279,Arsenic trichloride,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5140,T3D0279,Arsenic trichloride,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5141,T3D0282,Arsenous acid,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5142,T3D0282,Arsenous acid,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5143,T3D0282,Arsenous acid,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5144,T3D0282,Arsenous acid,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5145,T3D0282,Arsenous acid,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5146,T3D0282,Arsenous acid,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5147,T3D0282,Arsenous acid,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5148,T3D0282,Arsenous acid,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5149,T3D0282,Arsenous acid,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5150,T3D0282,Arsenous acid,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5151,T3D0282,Arsenous acid,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5152,T3D0282,Arsenous acid,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5153,T3D0282,Arsenous acid,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5154,T3D0282,Arsenous acid,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5155,T3D0282,Arsenous acid,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5156,T3D0282,Arsenous acid,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5157,T3D0282,Arsenous acid,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5158,T3D0282,Arsenous acid,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5159,T3D0283,Arsenenic acid,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5160,T3D0283,Arsenenic acid,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5161,T3D0283,Arsenenic acid,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5162,T3D0283,Arsenenic acid,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5163,T3D0283,Arsenenic acid,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5164,T3D0283,Arsenenic acid,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5165,T3D0283,Arsenenic acid,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5166,T3D0283,Arsenenic acid,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5167,T3D0283,Arsenenic acid,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5168,T3D0283,Arsenenic acid,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5169,T3D0283,Arsenenic acid,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5170,T3D0283,Arsenenic acid,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5171,T3D0283,Arsenenic acid,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5172,T3D0283,Arsenenic acid,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5173,T3D0283,Arsenenic acid,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5174,T3D0283,Arsenenic acid,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5175,T3D0283,Arsenenic acid,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5176,T3D0285,Ammonium arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5177,T3D0285,Ammonium arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5178,T3D0285,Ammonium arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5179,T3D0285,Ammonium arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5180,T3D0285,Ammonium arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5181,T3D0285,Ammonium arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5182,T3D0285,Ammonium arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5183,T3D0285,Ammonium arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5184,T3D0285,Ammonium arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5185,T3D0285,Ammonium arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5186,T3D0285,Ammonium arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5187,T3D0285,Ammonium arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5188,T3D0285,Ammonium arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5189,T3D0285,Ammonium arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5190,T3D0285,Ammonium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5191,T3D0285,Ammonium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5192,T3D0285,Ammonium arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5211,T3D0286,Copper(II) arsenite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5216,T3D0286,Copper(II) arsenite,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
5217,T3D0287,Gallium arsenide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5218,T3D0287,Gallium arsenide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5219,T3D0287,Gallium arsenide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5220,T3D0287,Gallium arsenide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5221,T3D0287,Gallium arsenide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5222,T3D0287,Gallium arsenide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5223,T3D0287,Gallium arsenide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5224,T3D0287,Gallium arsenide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5225,T3D0287,Gallium arsenide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5226,T3D0287,Gallium arsenide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5227,T3D0287,Gallium arsenide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5228,T3D0287,Gallium arsenide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5229,T3D0287,Gallium arsenide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5230,T3D0287,Gallium arsenide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5231,T3D0287,Gallium arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5232,T3D0287,Gallium arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5233,T3D0287,Gallium arsenide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5234,T3D0288,Copper arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5235,T3D0288,Copper arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5236,T3D0288,Copper arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5237,T3D0288,Copper arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5238,T3D0288,Copper arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5239,T3D0288,Copper arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5240,T3D0288,Copper arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5241,T3D0288,Copper arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5242,T3D0288,Copper arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5243,T3D0288,Copper arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5244,T3D0288,Copper arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5245,T3D0288,Copper arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5246,T3D0288,Copper arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5247,T3D0288,Copper arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5249,T3D0288,Copper arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5250,T3D0288,Copper arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5251,T3D0288,Copper arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5252,T3D0288,Copper arsenate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
5253,T3D0288,Copper arsenate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
5254,T3D0288,Copper arsenate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
5255,T3D0288,Copper arsenate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
5256,T3D0288,Copper arsenate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
5257,T3D0289,Copper arsenate hydroxide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5258,T3D0289,Copper arsenate hydroxide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5259,T3D0289,Copper arsenate hydroxide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5260,T3D0289,Copper arsenate hydroxide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5261,T3D0289,Copper arsenate hydroxide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5262,T3D0289,Copper arsenate hydroxide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5263,T3D0289,Copper arsenate hydroxide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5264,T3D0289,Copper arsenate hydroxide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5265,T3D0289,Copper arsenate hydroxide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5266,T3D0289,Copper arsenate hydroxide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5267,T3D0289,Copper arsenate hydroxide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5268,T3D0289,Copper arsenate hydroxide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5269,T3D0289,Copper arsenate hydroxide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5270,T3D0289,Copper arsenate hydroxide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5272,T3D0289,Copper arsenate hydroxide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5273,T3D0289,Copper arsenate hydroxide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5274,T3D0289,Copper arsenate hydroxide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5276,T3D0289,Copper arsenate hydroxide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
5277,T3D0289,Copper arsenate hydroxide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
5278,T3D0289,Copper arsenate hydroxide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
5279,T3D0289,Copper arsenate hydroxide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
5280,T3D0289,Copper arsenate hydroxide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
5281,T3D0290,Potassium arsenite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5282,T3D0290,Potassium arsenite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5283,T3D0290,Potassium arsenite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5284,T3D0290,Potassium arsenite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5285,T3D0290,Potassium arsenite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5286,T3D0290,Potassium arsenite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5287,T3D0290,Potassium arsenite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5288,T3D0290,Potassium arsenite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5289,T3D0290,Potassium arsenite,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5290,T3D0290,Potassium arsenite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5291,T3D0290,Potassium arsenite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5292,T3D0290,Potassium arsenite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5293,T3D0290,Potassium arsenite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5294,T3D0290,Potassium arsenite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5296,T3D0290,Potassium arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5297,T3D0290,Potassium arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5298,T3D0290,Potassium arsenite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5299,T3D0292,Arsenic pentoxide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5300,T3D0292,Arsenic pentoxide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5301,T3D0292,Arsenic pentoxide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5302,T3D0292,Arsenic pentoxide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5303,T3D0292,Arsenic pentoxide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5304,T3D0292,Arsenic pentoxide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5305,T3D0292,Arsenic pentoxide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5306,T3D0292,Arsenic pentoxide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5307,T3D0292,Arsenic pentoxide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5308,T3D0292,Arsenic pentoxide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5309,T3D0292,Arsenic pentoxide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5310,T3D0292,Arsenic pentoxide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5311,T3D0292,Arsenic pentoxide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5312,T3D0292,Arsenic pentoxide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5314,T3D0292,Arsenic pentoxide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate, it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5315,T3D0292,Arsenic pentoxide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5316,T3D0292,Arsenic pentoxide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5317,T3D0293,Magnesium arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5318,T3D0293,Magnesium arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5319,T3D0293,Magnesium arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5320,T3D0293,Magnesium arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5321,T3D0293,Magnesium arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5322,T3D0293,Magnesium arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5323,T3D0293,Magnesium arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5324,T3D0293,Magnesium arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5325,T3D0293,Magnesium arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5326,T3D0293,Magnesium arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5327,T3D0293,Magnesium arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5328,T3D0293,Magnesium arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5329,T3D0293,Magnesium arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5330,T3D0293,Magnesium arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5331,T3D0293,Magnesium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5332,T3D0293,Magnesium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5333,T3D0293,Magnesium arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5334,T3D0293,Magnesium arsenate,Carbonic anhydrase 3,P07451,Magnesium arsenate binds to carbonic anhydrase 3 (S252).
5335,T3D0294,Manganese arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5336,T3D0294,Manganese arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5337,T3D0294,Manganese arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5338,T3D0294,Manganese arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5339,T3D0294,Manganese arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5340,T3D0294,Manganese arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5341,T3D0294,Manganese arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5342,T3D0294,Manganese arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5343,T3D0294,Manganese arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5344,T3D0294,Manganese arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5345,T3D0294,Manganese arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5346,T3D0294,Manganese arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5347,T3D0294,Manganese arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5348,T3D0294,Manganese arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5349,T3D0294,Manganese arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5350,T3D0294,Manganese arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5351,T3D0294,Manganese arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5352,T3D0294,Manganese arsenate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
5353,T3D0294,Manganese arsenate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
5354,T3D0294,Manganese arsenate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
5355,T3D0294,Manganese arsenate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
5356,T3D0294,Manganese arsenate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
5357,T3D0296,Lead arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5358,T3D0296,Lead arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5359,T3D0296,Lead arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5360,T3D0296,Lead arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5361,T3D0296,Lead arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5362,T3D0296,Lead arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5363,T3D0296,Lead arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5364,T3D0296,Lead arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5365,T3D0296,Lead arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5366,T3D0296,Lead arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5367,T3D0296,Lead arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5368,T3D0296,Lead arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5369,T3D0296,Lead arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5370,T3D0296,Lead arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5371,T3D0296,Lead arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5372,T3D0296,Lead arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5373,T3D0296,Lead arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5374,T3D0296,Lead arsenate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5375,T3D0296,Lead arsenate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5376,T3D0296,Lead arsenate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5377,T3D0296,Lead arsenate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5378,T3D0296,Lead arsenate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5379,T3D0296,Lead arsenate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5380,T3D0296,Lead arsenate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5381,T3D0296,Lead arsenate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5382,T3D0296,Lead arsenate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5383,T3D0296,Lead arsenate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5384,T3D0296,Lead arsenate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5385,T3D0296,Lead arsenate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5386,T3D0296,Lead arsenate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5387,T3D0296,Lead arsenate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5388,T3D0296,Lead arsenate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5389,T3D0296,Lead arsenate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5390,T3D0296,Lead arsenate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5391,T3D0296,Lead arsenate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5392,T3D0296,Lead arsenate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5393,T3D0296,Lead arsenate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5394,T3D0296,Lead arsenate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5395,T3D0296,Lead arsenate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5396,T3D0296,Lead arsenate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5397,T3D0296,Lead arsenate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5398,T3D0296,Lead arsenate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
5399,T3D0296,Lead arsenate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5400,T3D0296,Lead arsenate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5401,T3D0296,Lead arsenate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5402,T3D0296,Lead arsenate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5403,T3D0297,Potassium arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5404,T3D0297,Potassium arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5405,T3D0297,Potassium arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5406,T3D0297,Potassium arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5407,T3D0297,Potassium arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5408,T3D0297,Potassium arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5409,T3D0297,Potassium arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5410,T3D0297,Potassium arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5411,T3D0297,Potassium arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5412,T3D0297,Potassium arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5413,T3D0297,Potassium arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5414,T3D0297,Potassium arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5415,T3D0297,Potassium arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5416,T3D0297,Potassium arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5417,T3D0297,Potassium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5418,T3D0297,Potassium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5419,T3D0297,Potassium arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5420,T3D0298,Sodium arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5421,T3D0298,Sodium arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5422,T3D0298,Sodium arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5423,T3D0298,Sodium arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5424,T3D0298,Sodium arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5425,T3D0298,Sodium arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5426,T3D0298,Sodium arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5427,T3D0298,Sodium arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5428,T3D0298,Sodium arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5429,T3D0298,Sodium arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5430,T3D0298,Sodium arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5431,T3D0298,Sodium arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5432,T3D0298,Sodium arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5433,T3D0298,Sodium arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5434,T3D0298,Sodium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5435,T3D0298,Sodium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5436,T3D0298,Sodium arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5437,T3D0299,Zinc arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5438,T3D0299,Zinc arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5439,T3D0299,Zinc arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5440,T3D0299,Zinc arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5441,T3D0299,Zinc arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5442,T3D0299,Zinc arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5443,T3D0299,Zinc arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5444,T3D0299,Zinc arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5445,T3D0299,Zinc arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5446,T3D0299,Zinc arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5447,T3D0299,Zinc arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5448,T3D0299,Zinc arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5449,T3D0299,Zinc arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5450,T3D0299,Zinc arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5452,T3D0299,Zinc arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5453,T3D0299,Zinc arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5454,T3D0299,Zinc arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5455,T3D0301,Arsenobetaine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5456,T3D0301,Arsenobetaine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5457,T3D0301,Arsenobetaine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5458,T3D0301,Arsenobetaine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5459,T3D0301,Arsenobetaine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5460,T3D0301,Arsenobetaine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5461,T3D0301,Arsenobetaine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5462,T3D0301,Arsenobetaine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5463,T3D0301,Arsenobetaine,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5464,T3D0301,Arsenobetaine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5465,T3D0301,Arsenobetaine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5466,T3D0301,Arsenobetaine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5467,T3D0301,Arsenobetaine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5468,T3D0301,Arsenobetaine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5469,T3D0301,Arsenobetaine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5470,T3D0301,Arsenobetaine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5471,T3D0301,Arsenobetaine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5472,T3D0302,Arsenocholine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5473,T3D0302,Arsenocholine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5474,T3D0302,Arsenocholine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5475,T3D0302,Arsenocholine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5476,T3D0302,Arsenocholine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5477,T3D0302,Arsenocholine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5478,T3D0302,Arsenocholine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5479,T3D0302,Arsenocholine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5480,T3D0302,Arsenocholine,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5481,T3D0302,Arsenocholine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5482,T3D0302,Arsenocholine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5483,T3D0302,Arsenocholine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5484,T3D0302,Arsenocholine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5485,T3D0302,Arsenocholine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5486,T3D0302,Arsenocholine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5487,T3D0302,Arsenocholine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5488,T3D0302,Arsenocholine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5489,T3D0303,Methylarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5490,T3D0303,Methylarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5491,T3D0303,Methylarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5492,T3D0303,Methylarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5493,T3D0303,Methylarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5494,T3D0303,Methylarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5495,T3D0303,Methylarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5496,T3D0303,Methylarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5497,T3D0303,Methylarsine,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5498,T3D0303,Methylarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5499,T3D0303,Methylarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5500,T3D0303,Methylarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5501,T3D0303,Methylarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5502,T3D0303,Methylarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5503,T3D0303,Methylarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5504,T3D0303,Methylarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5505,T3D0303,Methylarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5506,T3D0304,Dimethylarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5507,T3D0304,Dimethylarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5508,T3D0304,Dimethylarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5509,T3D0304,Dimethylarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5510,T3D0304,Dimethylarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5511,T3D0304,Dimethylarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5512,T3D0304,Dimethylarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5513,T3D0304,Dimethylarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5514,T3D0304,Dimethylarsine,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5515,T3D0304,Dimethylarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5516,T3D0304,Dimethylarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5517,T3D0304,Dimethylarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5518,T3D0304,Dimethylarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5519,T3D0304,Dimethylarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5520,T3D0304,Dimethylarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5521,T3D0304,Dimethylarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5522,T3D0304,Dimethylarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5523,T3D0305,Trimethylarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5524,T3D0305,Trimethylarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5525,T3D0305,Trimethylarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5526,T3D0305,Trimethylarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5527,T3D0305,Trimethylarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5528,T3D0305,Trimethylarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5529,T3D0305,Trimethylarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5530,T3D0305,Trimethylarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5531,T3D0305,Trimethylarsine,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5532,T3D0305,Trimethylarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5533,T3D0305,Trimethylarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5534,T3D0305,Trimethylarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5535,T3D0305,Trimethylarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5536,T3D0305,Trimethylarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5537,T3D0305,Trimethylarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5538,T3D0305,Trimethylarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5539,T3D0305,Trimethylarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5540,T3D0307,Methylarsonic acid,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5541,T3D0307,Methylarsonic acid,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5542,T3D0307,Methylarsonic acid,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5543,T3D0307,Methylarsonic acid,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5544,T3D0307,Methylarsonic acid,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5545,T3D0307,Methylarsonic acid,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5546,T3D0307,Methylarsonic acid,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5547,T3D0307,Methylarsonic acid,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5548,T3D0307,Methylarsonic acid,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5549,T3D0307,Methylarsonic acid,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5550,T3D0307,Methylarsonic acid,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5551,T3D0307,Methylarsonic acid,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5552,T3D0307,Methylarsonic acid,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5553,T3D0307,Methylarsonic acid,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5554,T3D0307,Methylarsonic acid,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5555,T3D0307,Methylarsonic acid,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5556,T3D0307,Methylarsonic acid,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5557,T3D0308,"Methylarsonic acid, disodium salt","Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5558,T3D0308,"Methylarsonic acid, disodium salt","Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5559,T3D0308,"Methylarsonic acid, disodium salt","Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5560,T3D0308,"Methylarsonic acid, disodium salt","Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5561,T3D0308,"Methylarsonic acid, disodium salt","Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5562,T3D0308,"Methylarsonic acid, disodium salt","Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5563,T3D0308,"Methylarsonic acid, disodium salt","Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5564,T3D0308,"Methylarsonic acid, disodium salt",DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5565,T3D0308,"Methylarsonic acid, disodium salt",Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5566,T3D0308,"Methylarsonic acid, disodium salt",Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5567,T3D0308,"Methylarsonic acid, disodium salt","Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5568,T3D0308,"Methylarsonic acid, disodium salt",Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5569,T3D0308,"Methylarsonic acid, disodium salt",Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5570,T3D0308,"Methylarsonic acid, disodium salt",Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5571,T3D0308,"Methylarsonic acid, disodium salt","Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5572,T3D0308,"Methylarsonic acid, disodium salt","Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5573,T3D0308,"Methylarsonic acid, disodium salt","Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5574,T3D0309,"Methylarsonic acid, monosodium salt","Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5575,T3D0309,"Methylarsonic acid, monosodium salt","Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5576,T3D0309,"Methylarsonic acid, monosodium salt","Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5577,T3D0309,"Methylarsonic acid, monosodium salt","Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5578,T3D0309,"Methylarsonic acid, monosodium salt","Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5579,T3D0309,"Methylarsonic acid, monosodium salt","Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5580,T3D0309,"Methylarsonic acid, monosodium salt","Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5581,T3D0309,"Methylarsonic acid, monosodium salt",DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5582,T3D0309,"Methylarsonic acid, monosodium salt",Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5583,T3D0309,"Methylarsonic acid, monosodium salt",Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5584,T3D0309,"Methylarsonic acid, monosodium salt","Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5585,T3D0309,"Methylarsonic acid, monosodium salt",Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5586,T3D0309,"Methylarsonic acid, monosodium salt",Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5587,T3D0309,"Methylarsonic acid, monosodium salt",Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5588,T3D0309,"Methylarsonic acid, monosodium salt","Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5589,T3D0309,"Methylarsonic acid, monosodium salt","Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5590,T3D0309,"Methylarsonic acid, monosodium salt","Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5608,T3D0318,Trimethylarsine oxide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5609,T3D0318,Trimethylarsine oxide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5610,T3D0318,Trimethylarsine oxide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5611,T3D0318,Trimethylarsine oxide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5612,T3D0318,Trimethylarsine oxide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5613,T3D0318,Trimethylarsine oxide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5614,T3D0318,Trimethylarsine oxide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5615,T3D0318,Trimethylarsine oxide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5616,T3D0318,Trimethylarsine oxide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5617,T3D0318,Trimethylarsine oxide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5618,T3D0318,Trimethylarsine oxide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5619,T3D0318,Trimethylarsine oxide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5620,T3D0318,Trimethylarsine oxide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5621,T3D0318,Trimethylarsine oxide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5622,T3D0318,Trimethylarsine oxide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5623,T3D0318,Trimethylarsine oxide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5624,T3D0318,Trimethylarsine oxide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5625,T3D0223,Arsenic acid,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5626,T3D0223,Arsenic acid,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5627,T3D0223,Arsenic acid,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5628,T3D0223,Arsenic acid,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5629,T3D0223,Arsenic acid,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5630,T3D0223,Arsenic acid,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5631,T3D0223,Arsenic acid,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5632,T3D0223,Arsenic acid,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5633,T3D0224,Arsenic trioxide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5634,T3D0224,Arsenic trioxide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5635,T3D0224,Arsenic trioxide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5636,T3D0224,Arsenic trioxide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5637,T3D0224,Arsenic trioxide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5638,T3D0224,Arsenic trioxide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5639,T3D0224,Arsenic trioxide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5640,T3D0224,Arsenic trioxide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5641,T3D0241,Calcium arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5642,T3D0241,Calcium arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5643,T3D0241,Calcium arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5644,T3D0241,Calcium arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5645,T3D0241,Calcium arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5646,T3D0241,Calcium arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5647,T3D0241,Calcium arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5648,T3D0241,Calcium arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5649,T3D0243,Sodium arsenite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5650,T3D0243,Sodium arsenite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5651,T3D0243,Sodium arsenite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5652,T3D0243,Sodium arsenite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5653,T3D0243,Sodium arsenite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5654,T3D0243,Sodium arsenite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5655,T3D0243,Sodium arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5656,T3D0243,Sodium arsenite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5657,T3D0319,Lead acetate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5658,T3D0319,Lead acetate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5659,T3D0319,Lead acetate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5660,T3D0319,Lead acetate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5661,T3D0319,Lead acetate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5662,T3D0319,Lead acetate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5663,T3D0319,Lead acetate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5664,T3D0319,Lead acetate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5665,T3D0319,Lead acetate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5666,T3D0319,Lead acetate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5667,T3D0319,Lead acetate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5668,T3D0319,Lead acetate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5669,T3D0319,Lead acetate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5670,T3D0319,Lead acetate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5671,T3D0319,Lead acetate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5672,T3D0319,Lead acetate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5673,T3D0319,Lead acetate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5674,T3D0319,Lead acetate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5675,T3D0319,Lead acetate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5676,T3D0319,Lead acetate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5677,T3D0319,Lead acetate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5678,T3D0319,Lead acetate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5679,T3D0319,Lead acetate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5680,T3D0319,Lead acetate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5681,T3D0319,Lead acetate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
5682,T3D0319,Lead acetate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5683,T3D0319,Lead acetate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5684,T3D0319,Lead acetate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5685,T3D0319,Lead acetate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5686,T3D0320,Lead arsenite,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5687,T3D0320,Lead arsenite,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5688,T3D0320,Lead arsenite,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5689,T3D0320,Lead arsenite,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5690,T3D0320,Lead arsenite,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5691,T3D0320,Lead arsenite,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5692,T3D0320,Lead arsenite,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5693,T3D0320,Lead arsenite,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5694,T3D0320,Lead arsenite,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5695,T3D0320,Lead arsenite,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5696,T3D0320,Lead arsenite,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5697,T3D0320,Lead arsenite,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5698,T3D0320,Lead arsenite,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5699,T3D0320,Lead arsenite,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5700,T3D0320,Lead arsenite,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5701,T3D0320,Lead arsenite,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5702,T3D0320,Lead arsenite,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5703,T3D0320,Lead arsenite,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5704,T3D0320,Lead arsenite,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5705,T3D0320,Lead arsenite,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5706,T3D0320,Lead arsenite,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5707,T3D0320,Lead arsenite,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5708,T3D0320,Lead arsenite,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5709,T3D0320,Lead arsenite,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which funtions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5710,T3D0320,Lead arsenite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
5711,T3D0320,Lead arsenite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
5712,T3D0320,Lead arsenite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
5713,T3D0320,Lead arsenite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
5714,T3D0320,Lead arsenite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
5715,T3D0320,Lead arsenite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
5716,T3D0320,Lead arsenite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5717,T3D0320,Lead arsenite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
5718,T3D0320,Lead arsenite,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
5719,T3D0320,Lead arsenite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
5720,T3D0320,Lead arsenite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5721,T3D0320,Lead arsenite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
5722,T3D0320,Lead arsenite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
5723,T3D0320,Lead arsenite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
5724,T3D0320,Lead arsenite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
5725,T3D0320,Lead arsenite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
5726,T3D0320,Lead arsenite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5727,T3D0320,Lead arsenite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5728,T3D0320,Lead arsenite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5729,T3D0320,Lead arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5730,T3D0320,Lead arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5731,T3D0320,Lead arsenite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5732,T3D0320,Lead arsenite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
5733,T3D0320,Lead arsenite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5734,T3D0320,Lead arsenite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5735,T3D0320,Lead arsenite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
5736,T3D0320,Lead arsenite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5737,T3D0320,Lead arsenite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5738,T3D0320,Lead arsenite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5739,T3D0320,Lead arsenite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5740,T3D0320,Lead arsenite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5741,T3D0320,Lead arsenite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5742,T3D0320,Lead arsenite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5743,T3D0320,Lead arsenite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5744,T3D0320,Lead arsenite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5745,T3D0320,Lead arsenite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5746,T3D0320,Lead arsenite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5747,T3D0320,Lead arsenite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5748,T3D0320,Lead arsenite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5749,T3D0320,Lead arsenite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5750,T3D0320,Lead arsenite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5751,T3D0320,Lead arsenite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5752,T3D0320,Lead arsenite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5753,T3D0320,Lead arsenite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
5754,T3D0321,Lead azide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5755,T3D0321,Lead azide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5756,T3D0321,Lead azide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5757,T3D0321,Lead azide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5758,T3D0321,Lead azide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5759,T3D0321,Lead azide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5760,T3D0321,Lead azide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5761,T3D0321,Lead azide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5762,T3D0321,Lead azide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5763,T3D0321,Lead azide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5764,T3D0321,Lead azide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5765,T3D0321,Lead azide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5766,T3D0321,Lead azide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5767,T3D0321,Lead azide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5768,T3D0321,Lead azide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5769,T3D0321,Lead azide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5770,T3D0321,Lead azide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5771,T3D0321,Lead azide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5772,T3D0321,Lead azide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5773,T3D0321,Lead azide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5774,T3D0321,Lead azide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5775,T3D0321,Lead azide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5776,T3D0321,Lead azide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5777,T3D0321,Lead azide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which funtions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5778,T3D0322,Lead bromide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5779,T3D0322,Lead bromide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5780,T3D0322,Lead bromide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5781,T3D0322,Lead bromide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5782,T3D0322,Lead bromide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5783,T3D0322,Lead bromide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5784,T3D0322,Lead bromide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5785,T3D0322,Lead bromide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5786,T3D0322,Lead bromide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5787,T3D0322,Lead bromide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5788,T3D0322,Lead bromide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5789,T3D0322,Lead bromide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5790,T3D0322,Lead bromide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5791,T3D0322,Lead bromide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5792,T3D0322,Lead bromide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5793,T3D0322,Lead bromide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5794,T3D0322,Lead bromide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5795,T3D0322,Lead bromide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5796,T3D0322,Lead bromide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5797,T3D0322,Lead bromide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5798,T3D0322,Lead bromide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5799,T3D0322,Lead bromide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5800,T3D0322,Lead bromide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5801,T3D0322,Lead bromide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5802,T3D0323,Lead carbonate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5803,T3D0323,Lead carbonate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5804,T3D0323,Lead carbonate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5805,T3D0323,Lead carbonate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5806,T3D0323,Lead carbonate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5807,T3D0323,Lead carbonate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5808,T3D0323,Lead carbonate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5809,T3D0323,Lead carbonate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5810,T3D0323,Lead carbonate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5811,T3D0323,Lead carbonate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5812,T3D0323,Lead carbonate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5813,T3D0323,Lead carbonate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5814,T3D0323,Lead carbonate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5815,T3D0323,Lead carbonate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5816,T3D0323,Lead carbonate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5817,T3D0323,Lead carbonate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5818,T3D0323,Lead carbonate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5819,T3D0323,Lead carbonate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5820,T3D0323,Lead carbonate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5821,T3D0323,Lead carbonate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5822,T3D0323,Lead carbonate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5823,T3D0323,Lead carbonate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5824,T3D0323,Lead carbonate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to Sodium/potassium-transporting ATPase subunit beta-3. (R065)
5825,T3D0323,Lead carbonate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5826,T3D0324,Lead chloride,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5827,T3D0324,Lead chloride,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5828,T3D0324,Lead chloride,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5829,T3D0324,Lead chloride,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5830,T3D0324,Lead chloride,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5831,T3D0324,Lead chloride,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5832,T3D0324,Lead chloride,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5833,T3D0324,Lead chloride,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5834,T3D0324,Lead chloride,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5835,T3D0324,Lead chloride,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5836,T3D0324,Lead chloride,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5837,T3D0324,Lead chloride,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5838,T3D0324,Lead chloride,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5839,T3D0324,Lead chloride,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5840,T3D0324,Lead chloride,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5841,T3D0324,Lead chloride,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5842,T3D0324,Lead chloride,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5843,T3D0324,Lead chloride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5844,T3D0324,Lead chloride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5845,T3D0324,Lead chloride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5846,T3D0324,Lead chloride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5847,T3D0324,Lead chloride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5848,T3D0324,Lead chloride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5849,T3D0324,Lead chloride,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which funtions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5850,T3D0325,Lead chromate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5851,T3D0325,Lead chromate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5852,T3D0325,Lead chromate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5853,T3D0325,Lead chromate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5855,T3D0325,Lead chromate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5856,T3D0325,Lead chromate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5857,T3D0325,Lead chromate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5858,T3D0325,Lead chromate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5859,T3D0325,Lead chromate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5860,T3D0325,Lead chromate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5861,T3D0325,Lead chromate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5862,T3D0325,Lead chromate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5863,T3D0325,Lead chromate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5864,T3D0325,Lead chromate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5865,T3D0325,Lead chromate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5866,T3D0325,Lead chromate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5867,T3D0325,Lead chromate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5868,T3D0325,Lead chromate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5869,T3D0325,Lead chromate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5870,T3D0325,Lead chromate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5871,T3D0325,Lead chromate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5872,T3D0325,Lead chromate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5873,T3D0325,Lead chromate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5874,T3D0325,Lead chromate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5875,T3D0325,Lead chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
5876,T3D0325,Lead chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
5877,T3D0325,Lead chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
5878,T3D0325,Lead chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
5879,T3D0325,Lead chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
5880,T3D0326,Lead fluoroborate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5881,T3D0326,Lead fluoroborate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5882,T3D0326,Lead fluoroborate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5883,T3D0326,Lead fluoroborate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5884,T3D0326,Lead fluoroborate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5885,T3D0326,Lead fluoroborate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5886,T3D0326,Lead fluoroborate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5887,T3D0326,Lead fluoroborate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5888,T3D0326,Lead fluoroborate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5889,T3D0326,Lead fluoroborate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5890,T3D0326,Lead fluoroborate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5891,T3D0326,Lead fluoroborate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5892,T3D0326,Lead fluoroborate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5893,T3D0326,Lead fluoroborate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5894,T3D0326,Lead fluoroborate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5895,T3D0326,Lead fluoroborate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5896,T3D0326,Lead fluoroborate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5897,T3D0326,Lead fluoroborate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5898,T3D0326,Lead fluoroborate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5899,T3D0326,Lead fluoroborate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5900,T3D0326,Lead fluoroborate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5901,T3D0326,Lead fluoroborate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5902,T3D0326,Lead fluoroborate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5903,T3D0326,Lead fluoroborate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5904,T3D0327,Lead iodide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5905,T3D0327,Lead iodide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5906,T3D0327,Lead iodide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5907,T3D0327,Lead iodide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5908,T3D0327,Lead iodide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5909,T3D0327,Lead iodide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5910,T3D0327,Lead iodide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5911,T3D0327,Lead iodide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5912,T3D0327,Lead iodide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5913,T3D0327,Lead iodide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5914,T3D0327,Lead iodide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5915,T3D0327,Lead iodide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5916,T3D0327,Lead iodide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5917,T3D0327,Lead iodide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5918,T3D0327,Lead iodide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5919,T3D0327,Lead iodide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5920,T3D0327,Lead iodide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5921,T3D0327,Lead iodide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5922,T3D0327,Lead iodide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5923,T3D0327,Lead iodide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5924,T3D0327,Lead iodide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5925,T3D0327,Lead iodide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5926,T3D0327,Lead iodide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5927,T3D0327,Lead iodide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5928,T3D0328,Lead molybdenum chromate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5929,T3D0328,Lead molybdenum chromate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5930,T3D0328,Lead molybdenum chromate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5931,T3D0328,Lead molybdenum chromate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5932,T3D0328,Lead molybdenum chromate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5933,T3D0328,Lead molybdenum chromate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5934,T3D0328,Lead molybdenum chromate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5935,T3D0328,Lead molybdenum chromate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5936,T3D0328,Lead molybdenum chromate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5937,T3D0328,Lead molybdenum chromate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5938,T3D0328,Lead molybdenum chromate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5939,T3D0328,Lead molybdenum chromate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5940,T3D0328,Lead molybdenum chromate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5941,T3D0328,Lead molybdenum chromate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5942,T3D0328,Lead molybdenum chromate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5943,T3D0328,Lead molybdenum chromate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5944,T3D0328,Lead molybdenum chromate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5945,T3D0328,Lead molybdenum chromate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5946,T3D0328,Lead molybdenum chromate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5947,T3D0328,Lead molybdenum chromate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5948,T3D0328,Lead molybdenum chromate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5949,T3D0328,Lead molybdenum chromate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5950,T3D0328,Lead molybdenum chromate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5951,T3D0328,Lead molybdenum chromate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5952,T3D0328,Lead molybdenum chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
5953,T3D0328,Lead molybdenum chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
5954,T3D0328,Lead molybdenum chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
5955,T3D0328,Lead molybdenum chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
5956,T3D0328,Lead molybdenum chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
5957,T3D0329,Lead nitrate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5958,T3D0329,Lead nitrate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5959,T3D0329,Lead nitrate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5960,T3D0329,Lead nitrate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5961,T3D0329,Lead nitrate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5962,T3D0329,Lead nitrate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5963,T3D0329,Lead nitrate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5964,T3D0329,Lead nitrate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5965,T3D0329,Lead nitrate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5966,T3D0329,Lead nitrate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5967,T3D0329,Lead nitrate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5968,T3D0329,Lead nitrate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5969,T3D0329,Lead nitrate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5970,T3D0329,Lead nitrate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5971,T3D0329,Lead nitrate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5972,T3D0329,Lead nitrate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5973,T3D0329,Lead nitrate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5974,T3D0329,Lead nitrate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5975,T3D0329,Lead nitrate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
5976,T3D0329,Lead nitrate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
5977,T3D0329,Lead nitrate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
5978,T3D0329,Lead nitrate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
5979,T3D0329,Lead nitrate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
5980,T3D0329,Lead nitrate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
5981,T3D0330,Lead oxide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
5982,T3D0330,Lead oxide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
5983,T3D0330,Lead oxide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5984,T3D0330,Lead oxide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
5985,T3D0330,Lead oxide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5986,T3D0330,Lead oxide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5987,T3D0330,Lead oxide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
5988,T3D0330,Lead oxide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5989,T3D0330,Lead oxide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5990,T3D0330,Lead oxide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5991,T3D0330,Lead oxide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5992,T3D0330,Lead oxide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5993,T3D0330,Lead oxide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5994,T3D0330,Lead oxide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5995,T3D0330,Lead oxide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5996,T3D0330,Lead oxide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
5997,T3D0330,Lead oxide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
5998,T3D0330,Lead oxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
5999,T3D0330,Lead oxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6000,T3D0330,Lead oxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6001,T3D0330,Lead oxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6002,T3D0330,Lead oxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6003,T3D0330,Lead oxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6004,T3D0330,Lead oxide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6005,T3D0331,Lead dioxide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
6006,T3D0331,Lead dioxide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
6007,T3D0331,Lead dioxide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6008,T3D0331,Lead dioxide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6009,T3D0331,Lead dioxide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6010,T3D0331,Lead dioxide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6011,T3D0331,Lead dioxide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6012,T3D0331,Lead dioxide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6013,T3D0331,Lead dioxide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6014,T3D0331,Lead dioxide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6015,T3D0331,Lead dioxide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6016,T3D0331,Lead dioxide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6017,T3D0331,Lead dioxide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6018,T3D0331,Lead dioxide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6019,T3D0331,Lead dioxide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6020,T3D0331,Lead dioxide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6021,T3D0331,Lead dioxide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
6022,T3D0331,Lead dioxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
6023,T3D0331,Lead dioxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6024,T3D0331,Lead dioxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6025,T3D0331,Lead dioxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6026,T3D0331,Lead dioxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6027,T3D0331,Lead dioxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6028,T3D0331,Lead dioxide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6029,T3D0332,Lead tetroxide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
6030,T3D0332,Lead tetroxide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
6031,T3D0332,Lead tetroxide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6032,T3D0332,Lead tetroxide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6033,T3D0332,Lead tetroxide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6034,T3D0332,Lead tetroxide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6035,T3D0332,Lead tetroxide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6036,T3D0332,Lead tetroxide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6037,T3D0332,Lead tetroxide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6038,T3D0332,Lead tetroxide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6039,T3D0332,Lead tetroxide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6040,T3D0332,Lead tetroxide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6041,T3D0332,Lead tetroxide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6042,T3D0332,Lead tetroxide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6043,T3D0332,Lead tetroxide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6044,T3D0332,Lead tetroxide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6045,T3D0332,Lead tetroxide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
6046,T3D0332,Lead tetroxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
6047,T3D0332,Lead tetroxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6048,T3D0332,Lead tetroxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6049,T3D0332,Lead tetroxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6050,T3D0332,Lead tetroxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6051,T3D0332,Lead tetroxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6052,T3D0332,Lead tetroxide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6053,T3D0333,Lead phosphate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
6054,T3D0333,Lead phosphate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
6055,T3D0333,Lead phosphate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6056,T3D0333,Lead phosphate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6057,T3D0333,Lead phosphate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6058,T3D0333,Lead phosphate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6059,T3D0333,Lead phosphate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6060,T3D0333,Lead phosphate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6061,T3D0333,Lead phosphate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6062,T3D0333,Lead phosphate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6063,T3D0333,Lead phosphate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6064,T3D0333,Lead phosphate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6065,T3D0333,Lead phosphate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6066,T3D0333,Lead phosphate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6067,T3D0333,Lead phosphate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6068,T3D0333,Lead phosphate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6069,T3D0333,Lead phosphate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
6070,T3D0333,Lead phosphate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
6071,T3D0333,Lead phosphate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6072,T3D0333,Lead phosphate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6073,T3D0333,Lead phosphate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6074,T3D0333,Lead phosphate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6075,T3D0333,Lead phosphate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6076,T3D0333,Lead phosphate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6077,T3D0334,Lead styphnate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
6078,T3D0334,Lead styphnate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
6079,T3D0334,Lead styphnate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6080,T3D0334,Lead styphnate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6081,T3D0334,Lead styphnate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6082,T3D0334,Lead styphnate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6083,T3D0334,Lead styphnate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6084,T3D0334,Lead styphnate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6085,T3D0334,Lead styphnate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6086,T3D0334,Lead styphnate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6087,T3D0334,Lead styphnate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6088,T3D0334,Lead styphnate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6089,T3D0334,Lead styphnate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6090,T3D0334,Lead styphnate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6091,T3D0334,Lead styphnate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6092,T3D0334,Lead styphnate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6093,T3D0334,Lead styphnate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
6094,T3D0334,Lead styphnate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
6095,T3D0334,Lead styphnate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6096,T3D0334,Lead styphnate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6098,T3D0334,Lead styphnate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6099,T3D0334,Lead styphnate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6100,T3D0334,Lead styphnate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6101,T3D0334,Lead styphnate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6102,T3D0335,Lead sulfate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
6103,T3D0335,Lead sulfate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
6104,T3D0335,Lead sulfate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6105,T3D0335,Lead sulfate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6106,T3D0335,Lead sulfate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6107,T3D0335,Lead sulfate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6108,T3D0335,Lead sulfate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6109,T3D0335,Lead sulfate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6110,T3D0335,Lead sulfate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6111,T3D0335,Lead sulfate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6112,T3D0335,Lead sulfate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6113,T3D0335,Lead sulfate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6114,T3D0335,Lead sulfate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6115,T3D0335,Lead sulfate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6116,T3D0335,Lead sulfate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6117,T3D0335,Lead sulfate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6118,T3D0335,Lead sulfate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
6119,T3D0335,Lead sulfate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
6120,T3D0335,Lead sulfate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6121,T3D0335,Lead sulfate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6122,T3D0335,Lead sulfate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6123,T3D0335,Lead sulfate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6124,T3D0335,Lead sulfate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6125,T3D0335,Lead sulfate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6126,T3D0336,Lead sulfide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
6127,T3D0336,Lead sulfide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
6128,T3D0336,Lead sulfide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6129,T3D0336,Lead sulfide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6130,T3D0336,Lead sulfide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6131,T3D0336,Lead sulfide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6132,T3D0336,Lead sulfide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6133,T3D0336,Lead sulfide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6134,T3D0336,Lead sulfide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6135,T3D0336,Lead sulfide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6136,T3D0336,Lead sulfide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6137,T3D0336,Lead sulfide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6138,T3D0336,Lead sulfide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6139,T3D0336,Lead sulfide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6140,T3D0336,Lead sulfide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6141,T3D0336,Lead sulfide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6142,T3D0336,Lead sulfide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
6143,T3D0336,Lead sulfide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
6144,T3D0336,Lead sulfide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6145,T3D0336,Lead sulfide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6146,T3D0336,Lead sulfide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6147,T3D0336,Lead sulfide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6148,T3D0336,Lead sulfide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6149,T3D0336,Lead sulfide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6150,T3D0337,Tetramethyl lead,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
6151,T3D0337,Tetramethyl lead,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
6152,T3D0337,Tetramethyl lead,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6153,T3D0337,Tetramethyl lead,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6154,T3D0337,Tetramethyl lead,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6155,T3D0337,Tetramethyl lead,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6156,T3D0337,Tetramethyl lead,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6157,T3D0337,Tetramethyl lead,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6158,T3D0337,Tetramethyl lead,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6159,T3D0337,Tetramethyl lead,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6160,T3D0337,Tetramethyl lead,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6161,T3D0337,Tetramethyl lead,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6162,T3D0337,Tetramethyl lead,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6163,T3D0337,Tetramethyl lead,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6164,T3D0337,Tetramethyl lead,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6165,T3D0337,Tetramethyl lead,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6166,T3D0337,Tetramethyl lead,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
6167,T3D0337,Tetramethyl lead,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
6168,T3D0337,Tetramethyl lead,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6169,T3D0337,Tetramethyl lead,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6170,T3D0337,Tetramethyl lead,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6171,T3D0337,Tetramethyl lead,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6172,T3D0337,Tetramethyl lead,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6173,T3D0337,Tetramethyl lead,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6174,T3D0338,Tetraethyl lead,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
6175,T3D0338,Tetraethyl lead,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
6176,T3D0338,Tetraethyl lead,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6177,T3D0338,Tetraethyl lead,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
6178,T3D0338,Tetraethyl lead,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6179,T3D0338,Tetraethyl lead,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6180,T3D0338,Tetraethyl lead,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
6181,T3D0338,Tetraethyl lead,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6182,T3D0338,Tetraethyl lead,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6183,T3D0338,Tetraethyl lead,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6184,T3D0338,Tetraethyl lead,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6185,T3D0338,Tetraethyl lead,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6186,T3D0338,Tetraethyl lead,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6187,T3D0338,Tetraethyl lead,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6188,T3D0338,Tetraethyl lead,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6189,T3D0338,Tetraethyl lead,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
6190,T3D0338,Tetraethyl lead,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
6191,T3D0338,Tetraethyl lead,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
6192,T3D0338,Tetraethyl lead,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
6193,T3D0338,Tetraethyl lead,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
6194,T3D0338,Tetraethyl lead,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
6195,T3D0338,Tetraethyl lead,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
6196,T3D0338,Tetraethyl lead,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
6197,T3D0338,Tetraethyl lead,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
6198,T3D0340,Mercury(II) fulminate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6199,T3D0340,Mercury(II) fulminate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6200,T3D0340,Mercury(II) fulminate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6201,T3D0340,Mercury(II) fulminate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6202,T3D0340,Mercury(II) fulminate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6203,T3D0340,Mercury(II) fulminate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6204,T3D0340,Mercury(II) fulminate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6205,T3D0340,Mercury(II) fulminate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6206,T3D0340,Mercury(II) fulminate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6207,T3D0340,Mercury(II) fulminate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6208,T3D0340,Mercury(II) fulminate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6209,T3D0340,Mercury(II) fulminate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6210,T3D0340,Mercury(II) fulminate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6211,T3D0340,Mercury(II) fulminate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6212,T3D0340,Mercury(II) fulminate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6213,T3D0340,Mercury(II) fulminate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6214,T3D0340,Mercury(II) fulminate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6215,T3D0340,Mercury(II) fulminate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6216,T3D0340,Mercury(II) fulminate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6217,T3D0340,Mercury(II) fulminate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6218,T3D0340,Mercury(II) fulminate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6219,T3D0340,Mercury(II) fulminate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6220,T3D0340,Mercury(II) fulminate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6221,T3D0340,Mercury(II) fulminate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6222,T3D0340,Mercury(II) fulminate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6223,T3D0340,Mercury(II) fulminate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6224,T3D0340,Mercury(II) fulminate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6225,T3D0340,Mercury(II) fulminate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6226,T3D0340,Mercury(II) fulminate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6227,T3D0340,Mercury(II) fulminate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6228,T3D0340,Mercury(II) fulminate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6229,T3D0340,Mercury(II) fulminate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6230,T3D0340,Mercury(II) fulminate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6231,T3D0340,Mercury(II) fulminate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6232,T3D0340,Mercury(II) fulminate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6233,T3D0340,Mercury(II) fulminate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6234,T3D0340,Mercury(II) fulminate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6235,T3D0340,Mercury(II) fulminate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6236,T3D0340,Mercury(II) fulminate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6237,T3D0340,Mercury(II) fulminate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6238,T3D0340,Mercury(II) fulminate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6239,T3D0340,Mercury(II) fulminate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6240,T3D0340,Mercury(II) fulminate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6241,T3D0340,Mercury(II) fulminate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6242,T3D0340,Mercury(II) fulminate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6243,T3D0340,Mercury(II) fulminate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6244,T3D0340,Mercury(II) fulminate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6245,T3D0340,Mercury(II) fulminate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6246,T3D0340,Mercury(II) fulminate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6247,T3D0341,Mercury(II) sulfide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6248,T3D0341,Mercury(II) sulfide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6249,T3D0341,Mercury(II) sulfide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6250,T3D0341,Mercury(II) sulfide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6251,T3D0341,Mercury(II) sulfide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6252,T3D0341,Mercury(II) sulfide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6253,T3D0341,Mercury(II) sulfide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6254,T3D0341,Mercury(II) sulfide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6255,T3D0341,Mercury(II) sulfide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6256,T3D0341,Mercury(II) sulfide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6257,T3D0341,Mercury(II) sulfide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6258,T3D0341,Mercury(II) sulfide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6259,T3D0341,Mercury(II) sulfide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6260,T3D0341,Mercury(II) sulfide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6261,T3D0341,Mercury(II) sulfide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6262,T3D0341,Mercury(II) sulfide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6263,T3D0341,Mercury(II) sulfide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6264,T3D0341,Mercury(II) sulfide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6265,T3D0341,Mercury(II) sulfide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6266,T3D0342,Mercury(II) oxide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6267,T3D0342,Mercury(II) oxide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6268,T3D0342,Mercury(II) oxide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6269,T3D0342,Mercury(II) oxide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6270,T3D0342,Mercury(II) oxide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6271,T3D0342,Mercury(II) oxide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6272,T3D0342,Mercury(II) oxide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6273,T3D0342,Mercury(II) oxide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6274,T3D0342,Mercury(II) oxide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6275,T3D0342,Mercury(II) oxide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6276,T3D0342,Mercury(II) oxide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6277,T3D0342,Mercury(II) oxide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6278,T3D0342,Mercury(II) oxide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6279,T3D0342,Mercury(II) oxide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6280,T3D0342,Mercury(II) oxide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6281,T3D0342,Mercury(II) oxide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6282,T3D0342,Mercury(II) oxide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6283,T3D0342,Mercury(II) oxide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6284,T3D0342,Mercury(II) oxide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6285,T3D0343,Mercury(I) chloride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6286,T3D0343,Mercury(I) chloride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6287,T3D0343,Mercury(I) chloride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6288,T3D0343,Mercury(I) chloride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6289,T3D0343,Mercury(I) chloride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6290,T3D0343,Mercury(I) chloride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6291,T3D0343,Mercury(I) chloride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6292,T3D0343,Mercury(I) chloride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6293,T3D0343,Mercury(I) chloride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6294,T3D0343,Mercury(I) chloride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6295,T3D0343,Mercury(I) chloride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6296,T3D0343,Mercury(I) chloride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6297,T3D0343,Mercury(I) chloride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6298,T3D0343,Mercury(I) chloride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6299,T3D0343,Mercury(I) chloride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6300,T3D0343,Mercury(I) chloride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6301,T3D0343,Mercury(I) chloride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6302,T3D0343,Mercury(I) chloride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6303,T3D0343,Mercury(I) chloride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6304,T3D0343,Mercury(I) chloride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6305,T3D0344,Phenylmercuric acetate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6306,T3D0344,Phenylmercuric acetate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6307,T3D0344,Phenylmercuric acetate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6308,T3D0344,Phenylmercuric acetate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6309,T3D0344,Phenylmercuric acetate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6310,T3D0344,Phenylmercuric acetate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6311,T3D0344,Phenylmercuric acetate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6312,T3D0344,Phenylmercuric acetate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6313,T3D0344,Phenylmercuric acetate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6314,T3D0344,Phenylmercuric acetate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6315,T3D0344,Phenylmercuric acetate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6316,T3D0344,Phenylmercuric acetate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6317,T3D0344,Phenylmercuric acetate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6318,T3D0344,Phenylmercuric acetate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6319,T3D0344,Phenylmercuric acetate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6320,T3D0344,Phenylmercuric acetate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6321,T3D0344,Phenylmercuric acetate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6322,T3D0344,Phenylmercuric acetate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6323,T3D0344,Phenylmercuric acetate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6324,T3D0345,Mercury selenide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6325,T3D0345,Mercury selenide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6326,T3D0345,Mercury selenide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6327,T3D0345,Mercury selenide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6328,T3D0345,Mercury selenide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6329,T3D0345,Mercury selenide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6330,T3D0345,Mercury selenide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6331,T3D0345,Mercury selenide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6332,T3D0345,Mercury selenide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6333,T3D0345,Mercury selenide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6334,T3D0345,Mercury selenide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6335,T3D0345,Mercury selenide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6336,T3D0345,Mercury selenide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6337,T3D0345,Mercury selenide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6338,T3D0345,Mercury selenide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6339,T3D0345,Mercury selenide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6340,T3D0345,Mercury selenide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6341,T3D0345,Mercury selenide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6342,T3D0345,Mercury selenide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6343,T3D0345,Mercury selenide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6344,T3D0346,Mercury telluride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6345,T3D0346,Mercury telluride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6346,T3D0346,Mercury telluride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6347,T3D0346,Mercury telluride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6348,T3D0346,Mercury telluride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6349,T3D0346,Mercury telluride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6350,T3D0346,Mercury telluride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6351,T3D0346,Mercury telluride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6352,T3D0346,Mercury telluride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6353,T3D0346,Mercury telluride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6354,T3D0346,Mercury telluride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6355,T3D0346,Mercury telluride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6356,T3D0346,Mercury telluride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6357,T3D0346,Mercury telluride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6358,T3D0346,Mercury telluride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6359,T3D0346,Mercury telluride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6360,T3D0346,Mercury telluride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6361,T3D0346,Mercury telluride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6362,T3D0346,Mercury telluride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6363,T3D0347,Mercury cadmium telluride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6364,T3D0347,Mercury cadmium telluride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6365,T3D0347,Mercury cadmium telluride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6366,T3D0347,Mercury cadmium telluride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6367,T3D0347,Mercury cadmium telluride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6368,T3D0347,Mercury cadmium telluride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6369,T3D0347,Mercury cadmium telluride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6370,T3D0347,Mercury cadmium telluride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6371,T3D0347,Mercury cadmium telluride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6372,T3D0347,Mercury cadmium telluride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6373,T3D0347,Mercury cadmium telluride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6374,T3D0347,Mercury cadmium telluride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6375,T3D0347,Mercury cadmium telluride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6376,T3D0347,Mercury cadmium telluride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6377,T3D0347,Mercury cadmium telluride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6378,T3D0347,Mercury cadmium telluride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6379,T3D0347,Mercury cadmium telluride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6381,T3D0347,Mercury cadmium telluride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6382,T3D0347,Mercury cadmium telluride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6383,T3D0347,Mercury cadmium telluride,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6384,T3D0347,Mercury cadmium telluride,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6385,T3D0347,Mercury cadmium telluride,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6386,T3D0347,Mercury cadmium telluride,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6387,T3D0347,Mercury cadmium telluride,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
6388,T3D0347,Mercury cadmium telluride,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
6389,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6390,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6391,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6392,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6393,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6394,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6395,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6396,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6397,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6398,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6399,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6400,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6401,T3D0347,Mercury cadmium telluride,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6402,T3D0348,Mercury(II) acetate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6403,T3D0348,Mercury(II) acetate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6404,T3D0348,Mercury(II) acetate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6405,T3D0348,Mercury(II) acetate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6406,T3D0348,Mercury(II) acetate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6407,T3D0348,Mercury(II) acetate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6408,T3D0348,Mercury(II) acetate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6409,T3D0348,Mercury(II) acetate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6410,T3D0348,Mercury(II) acetate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6411,T3D0348,Mercury(II) acetate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6412,T3D0348,Mercury(II) acetate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6413,T3D0348,Mercury(II) acetate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6414,T3D0348,Mercury(II) acetate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6415,T3D0348,Mercury(II) acetate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6416,T3D0348,Mercury(II) acetate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6417,T3D0348,Mercury(II) acetate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6418,T3D0348,Mercury(II) acetate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6419,T3D0348,Mercury(II) acetate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6420,T3D0348,Mercury(II) acetate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6421,T3D0348,Mercury(II) acetate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6422,T3D0349,Mercury(I) acetate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6423,T3D0349,Mercury(I) acetate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6424,T3D0349,Mercury(I) acetate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6425,T3D0349,Mercury(I) acetate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6426,T3D0349,Mercury(I) acetate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6427,T3D0349,Mercury(I) acetate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6428,T3D0349,Mercury(I) acetate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6429,T3D0349,Mercury(I) acetate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6430,T3D0349,Mercury(I) acetate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6431,T3D0349,Mercury(I) acetate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6432,T3D0349,Mercury(I) acetate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6433,T3D0349,Mercury(I) acetate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6434,T3D0349,Mercury(I) acetate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6435,T3D0349,Mercury(I) acetate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6436,T3D0349,Mercury(I) acetate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6437,T3D0349,Mercury(I) acetate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6438,T3D0349,Mercury(I) acetate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6439,T3D0349,Mercury(I) acetate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6440,T3D0349,Mercury(I) acetate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6441,T3D0350,Mercury(II) iodide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6442,T3D0350,Mercury(II) iodide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6443,T3D0350,Mercury(II) iodide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6444,T3D0350,Mercury(II) iodide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6445,T3D0350,Mercury(II) iodide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6446,T3D0350,Mercury(II) iodide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6447,T3D0350,Mercury(II) iodide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6448,T3D0350,Mercury(II) iodide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6449,T3D0350,Mercury(II) iodide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6450,T3D0350,Mercury(II) iodide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6451,T3D0350,Mercury(II) iodide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6452,T3D0350,Mercury(II) iodide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6453,T3D0350,Mercury(II) iodide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6454,T3D0350,Mercury(II) iodide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6455,T3D0350,Mercury(II) iodide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6456,T3D0350,Mercury(II) iodide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6457,T3D0350,Mercury(II) iodide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6459,T3D0350,Mercury(II) iodide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6460,T3D0350,Mercury(II) iodide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6461,T3D0351,Mercury(I) iodide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6462,T3D0351,Mercury(I) iodide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6463,T3D0351,Mercury(I) iodide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6464,T3D0351,Mercury(I) iodide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6465,T3D0351,Mercury(I) iodide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6466,T3D0351,Mercury(I) iodide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6467,T3D0351,Mercury(I) iodide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6468,T3D0351,Mercury(I) iodide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6469,T3D0351,Mercury(I) iodide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6470,T3D0351,Mercury(I) iodide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6471,T3D0351,Mercury(I) iodide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6472,T3D0351,Mercury(I) iodide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6473,T3D0351,Mercury(I) iodide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6474,T3D0351,Mercury(I) iodide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6475,T3D0351,Mercury(I) iodide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6476,T3D0351,Mercury(I) iodide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6477,T3D0351,Mercury(I) iodide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6479,T3D0351,Mercury(I) iodide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6480,T3D0351,Mercury(I) iodide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6481,T3D0351,Mercury(I) iodide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6482,T3D0352,Mercury(I) bromide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6483,T3D0352,Mercury(I) bromide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6484,T3D0352,Mercury(I) bromide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6485,T3D0352,Mercury(I) bromide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6486,T3D0352,Mercury(I) bromide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6487,T3D0352,Mercury(I) bromide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6488,T3D0352,Mercury(I) bromide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6489,T3D0352,Mercury(I) bromide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6490,T3D0352,Mercury(I) bromide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6491,T3D0352,Mercury(I) bromide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6492,T3D0352,Mercury(I) bromide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6493,T3D0352,Mercury(I) bromide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6494,T3D0352,Mercury(I) bromide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6495,T3D0352,Mercury(I) bromide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6496,T3D0352,Mercury(I) bromide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6497,T3D0352,Mercury(I) bromide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6498,T3D0352,Mercury(I) bromide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6500,T3D0352,Mercury(I) bromide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6501,T3D0352,Mercury(I) bromide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6502,T3D0353,Mercury(II) bromide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6503,T3D0353,Mercury(II) bromide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6504,T3D0353,Mercury(II) bromide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6505,T3D0353,Mercury(II) bromide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6506,T3D0353,Mercury(II) bromide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6507,T3D0353,Mercury(II) bromide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6508,T3D0353,Mercury(II) bromide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6509,T3D0353,Mercury(II) bromide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6510,T3D0353,Mercury(II) bromide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6511,T3D0353,Mercury(II) bromide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6512,T3D0353,Mercury(II) bromide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6513,T3D0353,Mercury(II) bromide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6514,T3D0353,Mercury(II) bromide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6515,T3D0353,Mercury(II) bromide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6516,T3D0353,Mercury(II) bromide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6517,T3D0353,Mercury(II) bromide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6518,T3D0353,Mercury(II) bromide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6520,T3D0353,Mercury(II) bromide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6521,T3D0353,Mercury(II) bromide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6522,T3D0354,Mercury(II) nitrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6523,T3D0354,Mercury(II) nitrate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6524,T3D0354,Mercury(II) nitrate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6525,T3D0354,Mercury(II) nitrate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6526,T3D0354,Mercury(II) nitrate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6527,T3D0354,Mercury(II) nitrate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6528,T3D0354,Mercury(II) nitrate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6529,T3D0354,Mercury(II) nitrate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6530,T3D0354,Mercury(II) nitrate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6531,T3D0354,Mercury(II) nitrate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6532,T3D0354,Mercury(II) nitrate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6533,T3D0354,Mercury(II) nitrate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6534,T3D0354,Mercury(II) nitrate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6535,T3D0354,Mercury(II) nitrate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6536,T3D0354,Mercury(II) nitrate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6537,T3D0354,Mercury(II) nitrate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6538,T3D0354,Mercury(II) nitrate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6540,T3D0354,Mercury(II) nitrate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6541,T3D0354,Mercury(II) nitrate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6542,T3D0355,Mercury(I) nitrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6543,T3D0355,Mercury(I) nitrate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6544,T3D0355,Mercury(I) nitrate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6545,T3D0355,Mercury(I) nitrate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6546,T3D0355,Mercury(I) nitrate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6547,T3D0355,Mercury(I) nitrate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6548,T3D0355,Mercury(I) nitrate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6549,T3D0355,Mercury(I) nitrate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6550,T3D0355,Mercury(I) nitrate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6551,T3D0355,Mercury(I) nitrate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6552,T3D0355,Mercury(I) nitrate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6553,T3D0355,Mercury(I) nitrate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6554,T3D0355,Mercury(I) nitrate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6555,T3D0355,Mercury(I) nitrate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6556,T3D0355,Mercury(I) nitrate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6557,T3D0355,Mercury(I) nitrate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6558,T3D0355,Mercury(I) nitrate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6559,T3D0355,Mercury(I) nitrate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6560,T3D0355,Mercury(I) nitrate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6561,T3D0356,Mercury(II) thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6562,T3D0356,Mercury(II) thiocyanate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6563,T3D0356,Mercury(II) thiocyanate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6564,T3D0356,Mercury(II) thiocyanate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6565,T3D0356,Mercury(II) thiocyanate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6566,T3D0356,Mercury(II) thiocyanate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6567,T3D0356,Mercury(II) thiocyanate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6568,T3D0356,Mercury(II) thiocyanate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6569,T3D0356,Mercury(II) thiocyanate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6570,T3D0356,Mercury(II) thiocyanate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6571,T3D0356,Mercury(II) thiocyanate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6572,T3D0356,Mercury(II) thiocyanate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6573,T3D0356,Mercury(II) thiocyanate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6574,T3D0356,Mercury(II) thiocyanate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6575,T3D0356,Mercury(II) thiocyanate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6576,T3D0356,Mercury(II) thiocyanate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6577,T3D0356,Mercury(II) thiocyanate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6578,T3D0356,Mercury(II) thiocyanate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6579,T3D0356,Mercury(II) thiocyanate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6580,T3D0356,Mercury(II) thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
6581,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6582,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6583,T3D0356,Mercury(II) thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6584,T3D0356,Mercury(II) thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6585,T3D0356,Mercury(II) thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6586,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6587,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6588,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6589,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6590,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6591,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6592,T3D0356,Mercury(II) thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6593,T3D0356,Mercury(II) thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6594,T3D0356,Mercury(II) thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6595,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6596,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6597,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6598,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6599,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6600,T3D0356,Mercury(II) thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6601,T3D0356,Mercury(II) thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
6602,T3D0356,Mercury(II) thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
6603,T3D0356,Mercury(II) thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
6604,T3D0356,Mercury(II) thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
6605,T3D0356,Mercury(II) thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
6606,T3D0356,Mercury(II) thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
6607,T3D0356,Mercury(II) thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
6608,T3D0356,Mercury(II) thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
6609,T3D0356,Mercury(II) thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
6610,T3D0356,Mercury(II) thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
6611,T3D0356,Mercury(II) thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
6612,T3D0356,Mercury(II) thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
6613,T3D0356,Mercury(II) thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
6614,T3D0356,Mercury(II) thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
6615,T3D0356,Mercury(II) thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
6616,T3D0356,Mercury(II) thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
6617,T3D0357,Mercury(II) sulfate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6618,T3D0357,Mercury(II) sulfate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6619,T3D0357,Mercury(II) sulfate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6620,T3D0357,Mercury(II) sulfate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6621,T3D0357,Mercury(II) sulfate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6622,T3D0357,Mercury(II) sulfate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6623,T3D0357,Mercury(II) sulfate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6624,T3D0357,Mercury(II) sulfate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6625,T3D0357,Mercury(II) sulfate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6626,T3D0357,Mercury(II) sulfate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6627,T3D0357,Mercury(II) sulfate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6628,T3D0357,Mercury(II) sulfate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6629,T3D0357,Mercury(II) sulfate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6630,T3D0357,Mercury(II) sulfate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6631,T3D0357,Mercury(II) sulfate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6632,T3D0357,Mercury(II) sulfate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6633,T3D0357,Mercury(II) sulfate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6634,T3D0357,Mercury(II) sulfate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6635,T3D0357,Mercury(II) sulfate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6636,T3D0358,Mercury(I) sulfate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6637,T3D0358,Mercury(I) sulfate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6638,T3D0358,Mercury(I) sulfate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6639,T3D0358,Mercury(I) sulfate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6640,T3D0358,Mercury(I) sulfate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6641,T3D0358,Mercury(I) sulfate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6642,T3D0358,Mercury(I) sulfate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6643,T3D0358,Mercury(I) sulfate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6644,T3D0358,Mercury(I) sulfate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6645,T3D0358,Mercury(I) sulfate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6646,T3D0358,Mercury(I) sulfate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6647,T3D0358,Mercury(I) sulfate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6648,T3D0358,Mercury(I) sulfate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6649,T3D0358,Mercury(I) sulfate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6650,T3D0358,Mercury(I) sulfate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6651,T3D0358,Mercury(I) sulfate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6652,T3D0358,Mercury(I) sulfate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6653,T3D0358,Mercury(I) sulfate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6654,T3D0358,Mercury(I) sulfate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6655,T3D0360,Methylmercuric chloride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6656,T3D0360,Methylmercuric chloride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6657,T3D0360,Methylmercuric chloride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6658,T3D0360,Methylmercuric chloride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6659,T3D0360,Methylmercuric chloride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6660,T3D0360,Methylmercuric chloride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6661,T3D0360,Methylmercuric chloride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6662,T3D0360,Methylmercuric chloride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6663,T3D0360,Methylmercuric chloride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6664,T3D0360,Methylmercuric chloride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6665,T3D0360,Methylmercuric chloride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6666,T3D0360,Methylmercuric chloride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6667,T3D0360,Methylmercuric chloride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6668,T3D0360,Methylmercuric chloride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6669,T3D0360,Methylmercuric chloride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6670,T3D0360,Methylmercuric chloride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6671,T3D0360,Methylmercuric chloride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6672,T3D0360,Methylmercuric chloride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6673,T3D0360,Methylmercuric chloride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6693,T3D0363,Mercury(II) cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6694,T3D0363,Mercury(II) cyanide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6695,T3D0363,Mercury(II) cyanide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6696,T3D0363,Mercury(II) cyanide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6697,T3D0363,Mercury(II) cyanide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6698,T3D0363,Mercury(II) cyanide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6699,T3D0363,Mercury(II) cyanide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6700,T3D0363,Mercury(II) cyanide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6701,T3D0363,Mercury(II) cyanide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6702,T3D0363,Mercury(II) cyanide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6703,T3D0363,Mercury(II) cyanide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6704,T3D0363,Mercury(II) cyanide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6705,T3D0363,Mercury(II) cyanide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6706,T3D0363,Mercury(II) cyanide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6707,T3D0363,Mercury(II) cyanide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6708,T3D0363,Mercury(II) cyanide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6709,T3D0363,Mercury(II) cyanide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6710,T3D0363,Mercury(II) cyanide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6711,T3D0363,Mercury(II) cyanide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
6713,T3D0363,Mercury(II) cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
6714,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6715,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6716,T3D0363,Mercury(II) cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6717,T3D0363,Mercury(II) cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6718,T3D0363,Mercury(II) cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6719,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6720,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6721,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6722,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6723,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6724,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6725,T3D0363,Mercury(II) cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6726,T3D0363,Mercury(II) cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6727,T3D0363,Mercury(II) cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6728,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6729,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6730,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6731,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6732,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6733,T3D0363,Mercury(II) cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
6734,T3D0363,Mercury(II) cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
6735,T3D0363,Mercury(II) cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
6736,T3D0363,Mercury(II) cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
6737,T3D0363,Mercury(II) cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
6738,T3D0363,Mercury(II) cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
6739,T3D0363,Mercury(II) cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
6740,T3D0363,Mercury(II) cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
6741,T3D0363,Mercury(II) cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
6742,T3D0363,Mercury(II) cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
6743,T3D0363,Mercury(II) cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
6744,T3D0363,Mercury(II) cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
6745,T3D0363,Mercury(II) cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
6746,T3D0363,Mercury(II) cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
6747,T3D0363,Mercury(II) cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
6748,T3D0363,Mercury(II) cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
6749,T3D0363,Mercury(II) cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
6750,T3D0242,Mercuric chloride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6751,T3D0242,Mercuric chloride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
6752,T3D0242,Mercuric chloride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6753,T3D0242,Mercuric chloride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6754,T3D0242,Mercuric chloride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6755,T3D0242,Mercuric chloride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6756,T3D0242,Mercuric chloride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6757,T3D0242,Mercuric chloride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6758,T3D0242,Mercuric chloride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6759,T3D0242,Mercuric chloride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6760,T3D0242,Mercuric chloride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
6761,T3D0364,Cadmium acetate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6762,T3D0364,Cadmium acetate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6763,T3D0364,Cadmium acetate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6764,T3D0364,Cadmium acetate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6765,T3D0364,Cadmium acetate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
6766,T3D0364,Cadmium acetate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
6767,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6768,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6769,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6770,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6771,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6772,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6773,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6774,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6775,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6776,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6777,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6778,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6779,T3D0364,Cadmium acetate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6780,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6781,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6782,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6783,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6784,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6785,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6786,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6787,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6788,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6789,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6790,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6791,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6792,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6793,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6794,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6795,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6796,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6797,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6798,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6799,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6800,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6801,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6802,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6803,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6804,T3D0367,Cadmium arsenide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
6805,T3D0367,Cadmium arsenide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
6806,T3D0367,Cadmium arsenide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
6807,T3D0367,Cadmium arsenide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
6808,T3D0367,Cadmium arsenide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
6809,T3D0367,Cadmium arsenide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
6810,T3D0367,Cadmium arsenide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
6811,T3D0367,Cadmium arsenide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
6812,T3D0367,Cadmium arsenide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
6813,T3D0367,Cadmium arsenide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
6814,T3D0367,Cadmium arsenide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
6815,T3D0367,Cadmium arsenide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
6816,T3D0367,Cadmium arsenide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
6817,T3D0367,Cadmium arsenide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
6818,T3D0367,Cadmium arsenide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
6819,T3D0367,Cadmium arsenide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
6820,T3D0367,Cadmium arsenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6821,T3D0367,Cadmium arsenide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6822,T3D0367,Cadmium arsenide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6823,T3D0367,Cadmium arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
6824,T3D0367,Cadmium arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
6825,T3D0367,Cadmium arsenide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
6826,T3D0367,Cadmium arsenide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
6827,T3D0367,Cadmium arsenide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
6828,T3D0367,Cadmium arsenide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
6829,T3D0367,Cadmium arsenide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
6830,T3D0367,Cadmium arsenide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6831,T3D0367,Cadmium arsenide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6832,T3D0367,Cadmium arsenide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6833,T3D0367,Cadmium arsenide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6834,T3D0367,Cadmium arsenide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6835,T3D0367,Cadmium arsenide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6836,T3D0367,Cadmium arsenide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6837,T3D0367,Cadmium arsenide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6838,T3D0367,Cadmium arsenide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6839,T3D0367,Cadmium arsenide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6840,T3D0367,Cadmium arsenide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6841,T3D0367,Cadmium arsenide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6842,T3D0367,Cadmium arsenide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6843,T3D0367,Cadmium arsenide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6844,T3D0367,Cadmium arsenide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6845,T3D0367,Cadmium arsenide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6846,T3D0367,Cadmium arsenide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6847,T3D0367,Cadmium arsenide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
6848,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6849,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6850,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6851,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6852,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6853,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6854,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6855,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6856,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6857,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6858,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6859,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6860,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6861,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6862,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6863,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6864,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6865,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6866,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6867,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6868,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6869,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6870,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6871,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6872,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6873,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6874,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6875,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6876,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6877,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6878,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6879,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6880,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6881,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6882,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6883,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6884,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6885,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6886,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6887,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6888,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6889,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6890,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6891,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6892,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6893,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6894,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6895,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6896,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6897,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6898,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6899,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6900,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6901,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6902,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6903,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6904,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6905,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6906,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6907,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6908,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6909,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6910,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6911,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6912,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6913,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6915,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6916,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6917,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6918,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6919,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6920,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6921,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6922,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6923,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6924,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6925,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6926,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6927,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6928,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6929,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6930,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6931,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6932,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6933,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6934,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6935,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6936,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6937,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6938,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6939,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6940,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6941,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6942,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6943,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6944,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6953,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6954,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6955,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6956,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6957,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6958,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6959,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6960,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6961,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6962,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6963,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6964,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6965,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6966,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6967,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6968,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6969,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6970,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6971,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6972,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6973,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6974,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6975,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6976,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6977,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6978,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6979,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6980,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6981,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6982,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6983,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6984,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6985,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6986,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6987,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6988,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6989,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6990,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6991,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6992,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6993,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6994,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6995,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6996,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6997,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6998,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
6999,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7000,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7001,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7002,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7003,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7004,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7005,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7006,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7007,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7008,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7009,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7010,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7011,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7012,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7013,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7014,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7015,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7016,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
7017,T3D0638,Basic beryllium acetate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7018,T3D0638,Basic beryllium acetate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7019,T3D0638,Basic beryllium acetate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7020,T3D0639,Beryllium acetate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7021,T3D0639,Beryllium acetate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7022,T3D0639,Beryllium acetate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7023,T3D0640,Beryllium bromide,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7024,T3D0640,Beryllium bromide,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7025,T3D0640,Beryllium bromide,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7026,T3D0641,Beryllium carbonate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7027,T3D0641,Beryllium carbonate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7028,T3D0641,Beryllium carbonate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7029,T3D0642,Beryllium chloride,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7030,T3D0642,Beryllium chloride,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7031,T3D0642,Beryllium chloride,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7032,T3D0643,Beryllium copper,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7033,T3D0643,Beryllium copper,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7034,T3D0643,Beryllium copper,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7035,T3D0643,Beryllium copper,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
7036,T3D0643,Beryllium copper,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
7037,T3D0643,Beryllium copper,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
7038,T3D0643,Beryllium copper,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
7039,T3D0643,Beryllium copper,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
7040,T3D0643,Beryllium copper,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
7041,T3D0644,Beryllium fluoride,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7042,T3D0644,Beryllium fluoride,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7043,T3D0644,Beryllium fluoride,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7044,T3D0645,Beryllium hydride,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7045,T3D0645,Beryllium hydride,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7046,T3D0645,Beryllium hydride,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7047,T3D0646,Beryllium hydroxide,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7048,T3D0646,Beryllium hydroxide,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7049,T3D0646,Beryllium hydroxide,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7050,T3D0647,Beryllium iodide,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7051,T3D0647,Beryllium iodide,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7052,T3D0647,Beryllium iodide,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7053,T3D0648,Beryllium oxide,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7054,T3D0648,Beryllium oxide,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7055,T3D0648,Beryllium oxide,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7056,T3D0649,Beryllium telluride,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7057,T3D0649,Beryllium telluride,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7058,T3D0649,Beryllium telluride,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7059,T3D0650,Beryllium phosphate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7060,T3D0650,Beryllium phosphate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7061,T3D0650,Beryllium phosphate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7062,T3D0651,Beryllium nitrate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7063,T3D0651,Beryllium nitrate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7064,T3D0651,Beryllium nitrate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7065,T3D0652,Beryllium sulfate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7066,T3D0652,Beryllium sulfate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7067,T3D0652,Beryllium sulfate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
7068,T3D0653,Cobalt(II) acetate,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7069,T3D0653,Cobalt(II) acetate,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7070,T3D0653,Cobalt(II) acetate,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7071,T3D0653,Cobalt(II) acetate,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7072,T3D0653,Cobalt(II) acetate,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7073,T3D0653,Cobalt(II) acetate,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7074,T3D0653,Cobalt(II) acetate,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7075,T3D0653,Cobalt(II) acetate,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7076,T3D0653,Cobalt(II) acetate,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7077,T3D0653,Cobalt(II) acetate,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7078,T3D0653,Cobalt(II) acetate,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7079,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-1 subunit,Q06432,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7080,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-2 subunit,Q9Y698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7081,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-3 subunit,O60359,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7082,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-4 subunit,Q9UBN1,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7083,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-5 subunit,Q9UF02,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7084,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-6 subunit,Q9BXT2,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7085,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-7 subunit,P62955,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7086,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7087,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7088,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel subunit alpha-2/delta-1,P54289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7089,T3D0653,Cobalt(II) acetate,"Calcium channel, alpha 2/delta subunit 2",Q9NY47,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7090,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel subunit alpha-2/delta-3,Q8IZS8,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7091,T3D0653,Cobalt(II) acetate,Voltage-dependent calcium channel subunit alpha-2/delta-4,Q7Z3S7,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7092,T3D0653,Cobalt(II) acetate,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7093,T3D0653,Cobalt(II) acetate,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7094,T3D0653,Cobalt(II) acetate,Voltage-dependent L-type calcium channel subunit alpha-1F,O60840,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7095,T3D0653,Cobalt(II) acetate,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7096,T3D0653,Cobalt(II) acetate,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7097,T3D0653,Cobalt(II) acetate,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7098,T3D0653,Cobalt(II) acetate,Voltage-dependent L-type calcium channel subunit beta-3,P54284,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7099,T3D0653,Cobalt(II) acetate,Voltage-dependent L-type calcium channel subunit beta-4,O00305,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7100,T3D0653,Cobalt(II) acetate,Voltage-dependent N-type calcium channel subunit alpha-1B,Q00975,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7101,T3D0653,Cobalt(II) acetate,Voltage-dependent P/Q-type calcium channel subunit alpha-1A,O00555,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7102,T3D0653,Cobalt(II) acetate,Voltage-dependent R-type calcium channel subunit alpha-1E,Q15878,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7103,T3D0654,Cobalt(III) acetate,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7104,T3D0654,Cobalt(III) acetate,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7105,T3D0654,Cobalt(III) acetate,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7106,T3D0654,Cobalt(III) acetate,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7107,T3D0654,Cobalt(III) acetate,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7108,T3D0654,Cobalt(III) acetate,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7109,T3D0654,Cobalt(III) acetate,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7110,T3D0654,Cobalt(III) acetate,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7111,T3D0654,Cobalt(III) acetate,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7112,T3D0654,Cobalt(III) acetate,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7113,T3D0654,Cobalt(III) acetate,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7114,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7115,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7116,T3D0654,Cobalt(III) acetate,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7117,T3D0654,Cobalt(III) acetate,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7118,T3D0654,Cobalt(III) acetate,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7119,T3D0654,Cobalt(III) acetate,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7120,T3D0654,Cobalt(III) acetate,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7121,T3D0655,Cobalt(II) carbonate,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7122,T3D0655,Cobalt(II) carbonate,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7123,T3D0655,Cobalt(II) carbonate,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7124,T3D0655,Cobalt(II) carbonate,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7125,T3D0655,Cobalt(II) carbonate,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7126,T3D0655,Cobalt(II) carbonate,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7127,T3D0655,Cobalt(II) carbonate,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7128,T3D0655,Cobalt(II) carbonate,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7129,T3D0655,Cobalt(II) carbonate,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7130,T3D0655,Cobalt(II) carbonate,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7131,T3D0655,Cobalt(II) carbonate,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7132,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7133,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7134,T3D0655,Cobalt(II) carbonate,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7135,T3D0655,Cobalt(II) carbonate,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7136,T3D0655,Cobalt(II) carbonate,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7137,T3D0655,Cobalt(II) carbonate,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7138,T3D0655,Cobalt(II) carbonate,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7139,T3D0658,Cobalt(II) bromide,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7140,T3D0658,Cobalt(II) bromide,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7141,T3D0658,Cobalt(II) bromide,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7142,T3D0658,Cobalt(II) bromide,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7143,T3D0658,Cobalt(II) bromide,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7144,T3D0658,Cobalt(II) bromide,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7145,T3D0658,Cobalt(II) bromide,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7146,T3D0658,Cobalt(II) bromide,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7147,T3D0658,Cobalt(II) bromide,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7148,T3D0658,Cobalt(II) bromide,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7149,T3D0658,Cobalt(II) bromide,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7150,T3D0658,Cobalt(II) bromide,Short transient receptor potential channel 4,Q9UBN4,Cobalt binds to Short transient receptor potential channel 4.
7151,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7152,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7153,T3D0658,Cobalt(II) bromide,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7154,T3D0658,Cobalt(II) bromide,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7155,T3D0658,Cobalt(II) bromide,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7156,T3D0658,Cobalt(II) bromide,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7157,T3D0658,Cobalt(II) bromide,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7158,T3D0659,Cobalt(II) chloride,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7159,T3D0659,Cobalt(II) chloride,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7160,T3D0659,Cobalt(II) chloride,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7161,T3D0659,Cobalt(II) chloride,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7162,T3D0659,Cobalt(II) chloride,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7163,T3D0659,Cobalt(II) chloride,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7164,T3D0659,Cobalt(II) chloride,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7165,T3D0659,Cobalt(II) chloride,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7166,T3D0659,Cobalt(II) chloride,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7167,T3D0659,Cobalt(II) chloride,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7168,T3D0659,Cobalt(II) chloride,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7169,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7170,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7171,T3D0659,Cobalt(II) chloride,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7172,T3D0659,Cobalt(II) chloride,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7173,T3D0659,Cobalt(II) chloride,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7174,T3D0659,Cobalt(II) chloride,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7175,T3D0659,Cobalt(II) chloride,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7176,T3D0660,Cobalt(II) fluoride,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7177,T3D0660,Cobalt(II) fluoride,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7178,T3D0660,Cobalt(II) fluoride,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7179,T3D0660,Cobalt(II) fluoride,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7180,T3D0660,Cobalt(II) fluoride,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7181,T3D0660,Cobalt(II) fluoride,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7182,T3D0660,Cobalt(II) fluoride,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7183,T3D0660,Cobalt(II) fluoride,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7184,T3D0660,Cobalt(II) fluoride,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7185,T3D0660,Cobalt(II) fluoride,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7186,T3D0660,Cobalt(II) fluoride,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7187,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7188,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7189,T3D0660,Cobalt(II) fluoride,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7190,T3D0660,Cobalt(II) fluoride,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7191,T3D0660,Cobalt(II) fluoride,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7192,T3D0660,Cobalt(II) fluoride,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7193,T3D0660,Cobalt(II) fluoride,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7194,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel subunit alpha-2/delta-1,P54289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7195,T3D0661,Cobalt(II) iodide,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7196,T3D0661,Cobalt(II) iodide,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7197,T3D0661,Cobalt(II) iodide,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7198,T3D0661,Cobalt(II) iodide,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7199,T3D0661,Cobalt(II) iodide,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7200,T3D0661,Cobalt(II) iodide,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7201,T3D0661,Cobalt(II) iodide,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7202,T3D0661,Cobalt(II) iodide,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7203,T3D0661,Cobalt(II) iodide,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7204,T3D0661,Cobalt(II) iodide,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7205,T3D0661,Cobalt(II) iodide,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7206,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7207,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7208,T3D0661,Cobalt(II) iodide,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7209,T3D0661,Cobalt(II) iodide,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7210,T3D0661,Cobalt(II) iodide,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7211,T3D0661,Cobalt(II) iodide,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7212,T3D0661,Cobalt(II) iodide,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7213,T3D0662,Cobalt(II) hydroxide,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7214,T3D0662,Cobalt(II) hydroxide,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7215,T3D0662,Cobalt(II) hydroxide,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7216,T3D0662,Cobalt(II) hydroxide,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7217,T3D0662,Cobalt(II) hydroxide,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7218,T3D0662,Cobalt(II) hydroxide,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7219,T3D0662,Cobalt(II) hydroxide,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7220,T3D0662,Cobalt(II) hydroxide,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7221,T3D0662,Cobalt(II) hydroxide,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7222,T3D0662,Cobalt(II) hydroxide,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7223,T3D0662,Cobalt(II) hydroxide,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7224,T3D0662,Cobalt(II) hydroxide,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7225,T3D0662,Cobalt(II) hydroxide,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7226,T3D0662,Cobalt(II) hydroxide,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7227,T3D0662,Cobalt(II) hydroxide,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7228,T3D0662,Cobalt(II) hydroxide,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7229,T3D0662,Cobalt(II) hydroxide,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7230,T3D0662,Cobalt(II) hydroxide,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7231,T3D0663,Cobalt(II) naphthenate,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7232,T3D0663,Cobalt(II) naphthenate,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7233,T3D0663,Cobalt(II) naphthenate,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7234,T3D0663,Cobalt(II) naphthenate,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7235,T3D0663,Cobalt(II) naphthenate,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7236,T3D0663,Cobalt(II) naphthenate,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7237,T3D0663,Cobalt(II) naphthenate,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7238,T3D0663,Cobalt(II) naphthenate,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7239,T3D0663,Cobalt(II) naphthenate,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7240,T3D0663,Cobalt(II) naphthenate,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7241,T3D0663,Cobalt(II) naphthenate,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7242,T3D0663,Cobalt(II) naphthenate,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7243,T3D0663,Cobalt(II) naphthenate,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7244,T3D0663,Cobalt(II) naphthenate,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7245,T3D0663,Cobalt(II) naphthenate,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7246,T3D0663,Cobalt(II) naphthenate,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7247,T3D0663,Cobalt(II) naphthenate,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7248,T3D0663,Cobalt(II) naphthenate,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7249,T3D0664,Cobalt(II) mesoporphyrin,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7250,T3D0664,Cobalt(II) mesoporphyrin,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7251,T3D0664,Cobalt(II) mesoporphyrin,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7252,T3D0664,Cobalt(II) mesoporphyrin,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7253,T3D0664,Cobalt(II) mesoporphyrin,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7254,T3D0664,Cobalt(II) mesoporphyrin,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7255,T3D0664,Cobalt(II) mesoporphyrin,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7256,T3D0664,Cobalt(II) mesoporphyrin,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7257,T3D0664,Cobalt(II) mesoporphyrin,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7258,T3D0664,Cobalt(II) mesoporphyrin,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7259,T3D0664,Cobalt(II) mesoporphyrin,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7260,T3D0664,Cobalt(II) mesoporphyrin,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7261,T3D0664,Cobalt(II) mesoporphyrin,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7262,T3D0664,Cobalt(II) mesoporphyrin,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7263,T3D0664,Cobalt(II) mesoporphyrin,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7264,T3D0664,Cobalt(II) mesoporphyrin,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7265,T3D0664,Cobalt(II) mesoporphyrin,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7266,T3D0664,Cobalt(II) mesoporphyrin,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7267,T3D0665,Cobalt(II) nitrate,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7268,T3D0665,Cobalt(II) nitrate,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7269,T3D0665,Cobalt(II) nitrate,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7270,T3D0665,Cobalt(II) nitrate,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7271,T3D0665,Cobalt(II) nitrate,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7272,T3D0665,Cobalt(II) nitrate,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7273,T3D0665,Cobalt(II) nitrate,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7274,T3D0665,Cobalt(II) nitrate,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7275,T3D0665,Cobalt(II) nitrate,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7276,T3D0665,Cobalt(II) nitrate,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7277,T3D0665,Cobalt(II) nitrate,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7278,T3D0665,Cobalt(II) nitrate,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7279,T3D0665,Cobalt(II) nitrate,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7280,T3D0665,Cobalt(II) nitrate,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7281,T3D0665,Cobalt(II) nitrate,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7282,T3D0665,Cobalt(II) nitrate,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7283,T3D0665,Cobalt(II) nitrate,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7284,T3D0665,Cobalt(II) nitrate,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7285,T3D0666,Cobalt(II) oxide,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7286,T3D0666,Cobalt(II) oxide,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7287,T3D0666,Cobalt(II) oxide,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7288,T3D0666,Cobalt(II) oxide,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7289,T3D0666,Cobalt(II) oxide,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7290,T3D0666,Cobalt(II) oxide,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7291,T3D0666,Cobalt(II) oxide,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7292,T3D0666,Cobalt(II) oxide,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7293,T3D0666,Cobalt(II) oxide,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7294,T3D0666,Cobalt(II) oxide,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7295,T3D0666,Cobalt(II) oxide,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7296,T3D0666,Cobalt(II) oxide,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7297,T3D0666,Cobalt(II) oxide,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7298,T3D0666,Cobalt(II) oxide,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7299,T3D0666,Cobalt(II) oxide,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7300,T3D0666,Cobalt(II) oxide,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7301,T3D0666,Cobalt(II) oxide,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7302,T3D0666,Cobalt(II) oxide,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7303,T3D0667,Cobalt(III) oxide,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7304,T3D0667,Cobalt(III) oxide,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7305,T3D0667,Cobalt(III) oxide,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7306,T3D0667,Cobalt(III) oxide,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7307,T3D0667,Cobalt(III) oxide,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7308,T3D0667,Cobalt(III) oxide,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7309,T3D0667,Cobalt(III) oxide,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7310,T3D0667,Cobalt(III) oxide,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7311,T3D0667,Cobalt(III) oxide,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7312,T3D0667,Cobalt(III) oxide,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7313,T3D0667,Cobalt(III) oxide,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7314,T3D0667,Cobalt(III) oxide,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7315,T3D0667,Cobalt(III) oxide,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7316,T3D0667,Cobalt(III) oxide,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7317,T3D0667,Cobalt(III) oxide,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7318,T3D0667,Cobalt(III) oxide,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7319,T3D0667,Cobalt(III) oxide,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7320,T3D0667,Cobalt(III) oxide,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7321,T3D0668,"Cobalt(II, III) oxide","5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7322,T3D0668,"Cobalt(II, III) oxide","5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7323,T3D0668,"Cobalt(II, III) oxide",Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7324,T3D0668,"Cobalt(II, III) oxide",Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7325,T3D0668,"Cobalt(II, III) oxide",Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7326,T3D0668,"Cobalt(II, III) oxide",DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7327,T3D0668,"Cobalt(II, III) oxide",DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7328,T3D0668,"Cobalt(II, III) oxide",Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7329,T3D0668,"Cobalt(II, III) oxide",Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7330,T3D0668,"Cobalt(II, III) oxide",Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7331,T3D0668,"Cobalt(II, III) oxide",Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7332,T3D0668,"Cobalt(II, III) oxide",Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7333,T3D0668,"Cobalt(II, III) oxide",Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7334,T3D0668,"Cobalt(II, III) oxide",Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7335,T3D0668,"Cobalt(II, III) oxide",Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7336,T3D0668,"Cobalt(II, III) oxide",Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7337,T3D0668,"Cobalt(II, III) oxide",Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7338,T3D0668,"Cobalt(II, III) oxide",Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7339,T3D0669,Cobalt(II) sulfate,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7340,T3D0669,Cobalt(II) sulfate,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7341,T3D0669,Cobalt(II) sulfate,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7342,T3D0669,Cobalt(II) sulfate,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7343,T3D0669,Cobalt(II) sulfate,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7344,T3D0669,Cobalt(II) sulfate,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7345,T3D0669,Cobalt(II) sulfate,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7346,T3D0669,Cobalt(II) sulfate,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7347,T3D0669,Cobalt(II) sulfate,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7348,T3D0669,Cobalt(II) sulfate,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7349,T3D0669,Cobalt(II) sulfate,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7350,T3D0669,Cobalt(II) sulfate,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7351,T3D0669,Cobalt(II) sulfate,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7352,T3D0669,Cobalt(II) sulfate,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7353,T3D0669,Cobalt(II) sulfate,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7354,T3D0669,Cobalt(II) sulfate,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7355,T3D0669,Cobalt(II) sulfate,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7356,T3D0669,Cobalt(II) sulfate,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7357,T3D0670,Cobalt(III) fluoride,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7358,T3D0670,Cobalt(III) fluoride,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7359,T3D0670,Cobalt(III) fluoride,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7360,T3D0670,Cobalt(III) fluoride,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7361,T3D0670,Cobalt(III) fluoride,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7362,T3D0670,Cobalt(III) fluoride,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7363,T3D0670,Cobalt(III) fluoride,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7364,T3D0670,Cobalt(III) fluoride,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7365,T3D0670,Cobalt(III) fluoride,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7366,T3D0670,Cobalt(III) fluoride,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7367,T3D0670,Cobalt(III) fluoride,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7368,T3D0670,Cobalt(III) fluoride,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7369,T3D0670,Cobalt(III) fluoride,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7370,T3D0670,Cobalt(III) fluoride,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7371,T3D0670,Cobalt(III) fluoride,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7372,T3D0670,Cobalt(III) fluoride,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7373,T3D0670,Cobalt(III) fluoride,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7374,T3D0670,Cobalt(III) fluoride,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7375,T3D0671,Cobaltocene,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7376,T3D0671,Cobaltocene,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7377,T3D0671,Cobaltocene,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7378,T3D0671,Cobaltocene,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7379,T3D0671,Cobaltocene,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7380,T3D0671,Cobaltocene,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7381,T3D0671,Cobaltocene,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7382,T3D0671,Cobaltocene,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7383,T3D0671,Cobaltocene,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7384,T3D0671,Cobaltocene,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7385,T3D0671,Cobaltocene,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7386,T3D0671,Cobaltocene,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7387,T3D0671,Cobaltocene,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7388,T3D0671,Cobaltocene,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7389,T3D0671,Cobaltocene,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7390,T3D0671,Cobaltocene,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7391,T3D0671,Cobaltocene,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7392,T3D0671,Cobaltocene,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7393,T3D0672,Cobamamide,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7394,T3D0672,Cobamamide,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7395,T3D0672,Cobamamide,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7396,T3D0672,Cobamamide,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7397,T3D0672,Cobamamide,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7398,T3D0672,Cobamamide,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7399,T3D0672,Cobamamide,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7400,T3D0672,Cobamamide,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7401,T3D0672,Cobamamide,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7402,T3D0672,Cobamamide,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7403,T3D0672,Cobamamide,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7404,T3D0672,Cobamamide,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7405,T3D0672,Cobamamide,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7407,T3D0672,Cobamamide,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7408,T3D0672,Cobamamide,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7409,T3D0672,Cobamamide,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7410,T3D0672,Cobamamide,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7411,T3D0672,Cobamamide,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7412,T3D0673,Cyanocobalamin,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7413,T3D0673,Cyanocobalamin,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7414,T3D0673,Cyanocobalamin,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7415,T3D0673,Cyanocobalamin,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7416,T3D0673,Cyanocobalamin,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7417,T3D0673,Cyanocobalamin,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7418,T3D0673,Cyanocobalamin,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7419,T3D0673,Cyanocobalamin,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7420,T3D0673,Cyanocobalamin,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7421,T3D0673,Cyanocobalamin,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7422,T3D0673,Cyanocobalamin,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7423,T3D0673,Cyanocobalamin,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7424,T3D0673,Cyanocobalamin,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7426,T3D0673,Cyanocobalamin,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7427,T3D0673,Cyanocobalamin,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7428,T3D0673,Cyanocobalamin,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7429,T3D0673,Cyanocobalamin,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7430,T3D0673,Cyanocobalamin,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7431,T3D0674,Dicobalt edetate,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7432,T3D0674,Dicobalt edetate,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7433,T3D0674,Dicobalt edetate,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7434,T3D0674,Dicobalt edetate,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7435,T3D0674,Dicobalt edetate,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7436,T3D0674,Dicobalt edetate,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7437,T3D0674,Dicobalt edetate,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7438,T3D0674,Dicobalt edetate,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7439,T3D0674,Dicobalt edetate,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7440,T3D0674,Dicobalt edetate,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7441,T3D0674,Dicobalt edetate,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7442,T3D0674,Dicobalt edetate,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7443,T3D0674,Dicobalt edetate,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7444,T3D0674,Dicobalt edetate,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7445,T3D0674,Dicobalt edetate,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7446,T3D0674,Dicobalt edetate,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7447,T3D0674,Dicobalt edetate,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7448,T3D0674,Dicobalt edetate,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7449,T3D0675,Dicobalt octacarbonyl,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7450,T3D0675,Dicobalt octacarbonyl,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7451,T3D0675,Dicobalt octacarbonyl,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7452,T3D0675,Dicobalt octacarbonyl,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7453,T3D0675,Dicobalt octacarbonyl,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7454,T3D0675,Dicobalt octacarbonyl,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7455,T3D0675,Dicobalt octacarbonyl,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7456,T3D0675,Dicobalt octacarbonyl,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7457,T3D0675,Dicobalt octacarbonyl,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7458,T3D0675,Dicobalt octacarbonyl,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7459,T3D0675,Dicobalt octacarbonyl,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7460,T3D0675,Dicobalt octacarbonyl,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7461,T3D0675,Dicobalt octacarbonyl,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7462,T3D0675,Dicobalt octacarbonyl,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7463,T3D0675,Dicobalt octacarbonyl,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7464,T3D0675,Dicobalt octacarbonyl,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7465,T3D0675,Dicobalt octacarbonyl,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7466,T3D0675,Dicobalt octacarbonyl,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7467,T3D0676,Hexamminecobalt(III) chloride,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7468,T3D0676,Hexamminecobalt(III) chloride,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7469,T3D0676,Hexamminecobalt(III) chloride,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7470,T3D0676,Hexamminecobalt(III) chloride,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7471,T3D0676,Hexamminecobalt(III) chloride,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7472,T3D0676,Hexamminecobalt(III) chloride,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7473,T3D0676,Hexamminecobalt(III) chloride,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7474,T3D0676,Hexamminecobalt(III) chloride,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7475,T3D0676,Hexamminecobalt(III) chloride,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7476,T3D0676,Hexamminecobalt(III) chloride,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7477,T3D0676,Hexamminecobalt(III) chloride,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7478,T3D0676,Hexamminecobalt(III) chloride,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7479,T3D0676,Hexamminecobalt(III) chloride,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7480,T3D0676,Hexamminecobalt(III) chloride,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7481,T3D0676,Hexamminecobalt(III) chloride,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7482,T3D0676,Hexamminecobalt(III) chloride,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7483,T3D0676,Hexamminecobalt(III) chloride,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7484,T3D0676,Hexamminecobalt(III) chloride,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7485,T3D0677,Hydroxocobalamin,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7486,T3D0677,Hydroxocobalamin,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7487,T3D0677,Hydroxocobalamin,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7488,T3D0677,Hydroxocobalamin,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7489,T3D0677,Hydroxocobalamin,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7490,T3D0677,Hydroxocobalamin,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7491,T3D0677,Hydroxocobalamin,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7492,T3D0677,Hydroxocobalamin,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7493,T3D0677,Hydroxocobalamin,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7494,T3D0677,Hydroxocobalamin,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7495,T3D0677,Hydroxocobalamin,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7496,T3D0677,Hydroxocobalamin,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7497,T3D0677,Hydroxocobalamin,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7498,T3D0677,Hydroxocobalamin,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7499,T3D0677,Hydroxocobalamin,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7500,T3D0677,Hydroxocobalamin,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7501,T3D0677,Hydroxocobalamin,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7502,T3D0677,Hydroxocobalamin,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7503,T3D0678,Lithium cobalt oxide,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7504,T3D0678,Lithium cobalt oxide,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7505,T3D0678,Lithium cobalt oxide,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7506,T3D0678,Lithium cobalt oxide,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7507,T3D0678,Lithium cobalt oxide,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7508,T3D0678,Lithium cobalt oxide,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7509,T3D0678,Lithium cobalt oxide,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7510,T3D0678,Lithium cobalt oxide,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7511,T3D0678,Lithium cobalt oxide,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7512,T3D0678,Lithium cobalt oxide,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7513,T3D0678,Lithium cobalt oxide,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7514,T3D0678,Lithium cobalt oxide,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7515,T3D0678,Lithium cobalt oxide,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7516,T3D0678,Lithium cobalt oxide,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7517,T3D0678,Lithium cobalt oxide,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7518,T3D0678,Lithium cobalt oxide,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7519,T3D0678,Lithium cobalt oxide,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7520,T3D0678,Lithium cobalt oxide,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7521,T3D0679,Methylcobalamin,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7522,T3D0679,Methylcobalamin,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7523,T3D0679,Methylcobalamin,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7524,T3D0679,Methylcobalamin,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7525,T3D0679,Methylcobalamin,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7526,T3D0679,Methylcobalamin,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7527,T3D0679,Methylcobalamin,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7528,T3D0679,Methylcobalamin,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7529,T3D0679,Methylcobalamin,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7530,T3D0679,Methylcobalamin,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7531,T3D0679,Methylcobalamin,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7532,T3D0679,Methylcobalamin,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7533,T3D0679,Methylcobalamin,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7534,T3D0679,Methylcobalamin,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7535,T3D0679,Methylcobalamin,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7536,T3D0679,Methylcobalamin,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7537,T3D0679,Methylcobalamin,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7538,T3D0679,Methylcobalamin,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7539,T3D0680,Salcomine,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7540,T3D0680,Salcomine,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7541,T3D0680,Salcomine,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7542,T3D0680,Salcomine,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7543,T3D0680,Salcomine,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7544,T3D0680,Salcomine,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7545,T3D0680,Salcomine,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7546,T3D0680,Salcomine,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7547,T3D0680,Salcomine,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7548,T3D0680,Salcomine,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7549,T3D0680,Salcomine,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7550,T3D0680,Salcomine,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7551,T3D0680,Salcomine,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7553,T3D0680,Salcomine,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7554,T3D0680,Salcomine,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7555,T3D0680,Salcomine,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7556,T3D0680,Salcomine,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7557,T3D0680,Salcomine,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7559,T3D0681,Sodium cobaltinitrite,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7560,T3D0681,Sodium cobaltinitrite,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7561,T3D0681,Sodium cobaltinitrite,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7562,T3D0681,Sodium cobaltinitrite,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7563,T3D0681,Sodium cobaltinitrite,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7564,T3D0681,Sodium cobaltinitrite,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7565,T3D0681,Sodium cobaltinitrite,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7566,T3D0681,Sodium cobaltinitrite,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7567,T3D0681,Sodium cobaltinitrite,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7568,T3D0681,Sodium cobaltinitrite,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7569,T3D0681,Sodium cobaltinitrite,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7570,T3D0681,Sodium cobaltinitrite,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7571,T3D0681,Sodium cobaltinitrite,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7572,T3D0681,Sodium cobaltinitrite,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7573,T3D0681,Sodium cobaltinitrite,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7574,T3D0681,Sodium cobaltinitrite,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7575,T3D0681,Sodium cobaltinitrite,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7576,T3D0681,Sodium cobaltinitrite,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7577,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,"5-aminolevulinate synthase, erythroid-specific, mitochondrial",P22557,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7578,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,"5-aminolevulinate synthase, nonspecific, mitochondrial",P13196,Cobalt inhibits heme synthesis by preventing synthesis of 5-aminolaevulinate via inhibition of 5-aminolaevulinate synthase. (R057)
7579,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Carbonic anhydrase 1,P00915,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7580,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Carbonic anhydrase 2,P00918,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7581,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Carbonic anhydrase 4,P22748,"Cobalt inhibits carbonic anhydrases.(R086, R248)"
7582,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,DNA,DNA,"Radioactive cobalt damages DNA, RNA, and lipids through ionizing events. (R084)"
7583,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,DNA repair protein complementing XP-A cells,P23025,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7584,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Ig alpha-1 chain C region,P01876,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7585,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Ig alpha-2 chain C region,P01877,"Cobalt interacts with specific IgA antibodies, resulting in immunosensitization. (R255)"
7586,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Ig epsilon chain C region,P01854,"Cobalt interacts with specific IgE antibodies, resulting in immunosensitization. (R254)"
7587,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Poly [ADP-ribose] polymerase 1,P09874,Cobalt inhibits DNA repair by interacting with zinc finger DNA repair proteins. (R256)
7588,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Voltage-dependent calcium channel gamma-8 subunit,Q8WXS5,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7589,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Voltage-dependent calcium channel gamma-like subunit,Q8WXS4,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7590,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Voltage-dependent L-type calcium channel subunit alpha-1C,Q13936,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7591,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Voltage-dependent L-type calcium channel subunit alpha-1D,Q01668,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7592,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Voltage-dependent L-type calcium channel subunit alpha-1S,Q13698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7593,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Voltage-dependent L-type calcium channel subunit beta-1,Q02641,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7594,T3D0682,Tris(ethylenediamine)cobalt(III) chloride,Voltage-dependent L-type calcium channel subunit beta-2,Q08289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
7595,T3D0683,Bis(cyclooctadiene)nickel(0),Alpha-ketoglutarate-dependent dioxygenase alkB homolog 2,Q6NS38,"Nickel substitutes for iron in alpha-ketoglutarate-dependent dioxygenases, inhibiting DNA repair. (R295)"
7596,T3D0683,Bis(cyclooctadiene)nickel(0),Alpha-ketoglutarate-dependent dioxygenase alkB homolog 3,Q96Q83,"Nickel substitutes for iron in alpha-ketoglutarate-dependent dioxygenases, inhibiting DNA repair. (R295)"
7597,T3D0683,Bis(cyclooctadiene)nickel(0),Calcineurin subunit B type 1,P63098,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7598,T3D0683,Bis(cyclooctadiene)nickel(0),Calcineurin subunit B isoform 2,Q96LZ3,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7599,T3D0683,Bis(cyclooctadiene)nickel(0),Egl nine homolog 1,Q9GZT9,"Nickel substitutes for iron in hypoxia-inducible factor prolyl hydroxylases, inhibiting their enzyme activity. This results in the accumulation of hypoxia inducible factor 1 alpha, causing hypoxia-mimic stress. (R295)"
7600,T3D0683,Bis(cyclooctadiene)nickel(0),Egl nine homolog 2,Q96KS0,"Nickel substitutes for iron in hypoxia-inducible factor prolyl hydroxylases, inhibiting their enzyme activity. This results in the accumulation of hypoxia inducible factor 1 alpha, causing hypoxia-mimic stress. (R295)"
7601,T3D0683,Bis(cyclooctadiene)nickel(0),Egl nine homolog 3,Q9H6Z9,"Nickel substitutes for iron in hypoxia-inducible factor prolyl hydroxylases, inhibiting their enzyme activity. This results in the accumulation of hypoxia inducible factor 1 alpha, causing hypoxia-mimic stress. (R295)"
7602,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1.0,P07305,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7603,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1.1,Q02539,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7604,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7605,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7606,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7607,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7608,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1oo,Q8IZA3,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7609,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1t,P22492,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7610,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H1x,Q92522,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7611,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 1,P0C0S8,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7612,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 1-A,Q96QV6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7613,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 1-B/E,P04908,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7614,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 1-C,Q93077,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7615,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 1-D,P20671,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7616,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 1-H,Q96KK5,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7617,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 1-J,Q99878,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7618,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 2-A,Q6FI13,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7619,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 2-B,Q8IUE6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7620,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 2-C,Q16777,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7621,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A type 3,Q7L7L0,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7622,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A-Bbd type 1,P0C5Y9,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7623,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A-Bbd type 2/3,P0C5Z0,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7624,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A.J,Q9BTM1,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7625,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A.V,Q71UI9,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7626,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A.x,P16104,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7627,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2A.Z,P0C0S5,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7628,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-A,Q96A08,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7629,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7630,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7631,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7632,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-H,Q93079,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7633,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-J,P06899,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7634,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-K,O60814,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7635,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7636,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7637,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7638,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 1-O,P23527,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7639,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 2-E,Q16778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7640,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 2-F,Q5QNW6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7641,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type 3-B,Q8N257,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7642,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type F-M,P0C1H6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7643,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type F-S,P57053,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7644,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H2B type W-T,Q7Z2G1,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7645,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H3-like,Q6NXT2,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7646,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7647,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7648,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H3.1t,Q16695,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7649,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H3.2,Q71DI3,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7650,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7651,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7652,T3D0683,Bis(cyclooctadiene)nickel(0),Histone H4-like protein type G,Q99525,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7653,T3D0683,Bis(cyclooctadiene)nickel(0),JmjC domain-containing histone demethylation protein 2A,Q9Y4C1,"Nickel substitutes for iron in jmjC domain-containing histone demethylation proteins, inhibiting their demethylation activity. (R295)"
7654,T3D0683,Bis(cyclooctadiene)nickel(0),JmjC domain-containing histone demethylation protein 3A,O75164,"Nickel substitutes for iron in jmjC domain-containing histone demethylation proteins, inhibiting their demethylation activity. (R295)"
7655,T3D0683,Bis(cyclooctadiene)nickel(0),Protamine-2,P04554,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7656,T3D0683,Bis(cyclooctadiene)nickel(0),Protamine-3,Q9NNZ6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7657,T3D0683,Bis(cyclooctadiene)nickel(0),Putative histone H2B type 2-D,Q6DRA6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7658,T3D0683,Bis(cyclooctadiene)nickel(0),Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform,Q08209,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7659,T3D0683,Bis(cyclooctadiene)nickel(0),Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7660,T3D0683,Bis(cyclooctadiene)nickel(0),Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7661,T3D0683,Bis(cyclooctadiene)nickel(0),Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7662,T3D0683,Bis(cyclooctadiene)nickel(0),Testis-specific H1 histone,Q75WM6,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7663,T3D0684,Nickel acetate,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7664,T3D0684,Nickel acetate,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7665,T3D0684,Nickel acetate,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7666,T3D0684,Nickel acetate,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7667,T3D0684,Nickel acetate,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7668,T3D0684,Nickel acetate,Histone H2B type 2-E,Q16778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7669,T3D0684,Nickel acetate,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7670,T3D0684,Nickel acetate,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7671,T3D0684,Nickel acetate,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7672,T3D0684,Nickel acetate,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7673,T3D0684,Nickel acetate,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7674,T3D0684,Nickel acetate,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7675,T3D0684,Nickel acetate,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7676,T3D0684,Nickel acetate,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7677,T3D0684,Nickel acetate,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7678,T3D0684,Nickel acetate,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7679,T3D0684,Nickel acetate,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7680,T3D0684,Nickel acetate,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7685,T3D0685,Nickel ammonium sulfate hexahydrate,Histone H2B type 1-H,Q93079,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7699,T3D0686,Nickel carbonate,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7700,T3D0686,Nickel carbonate,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7701,T3D0686,Nickel carbonate,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7702,T3D0686,Nickel carbonate,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7704,T3D0686,Nickel carbonate,Histone H2A type 1,P0C0S8,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7705,T3D0686,Nickel carbonate,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7706,T3D0686,Nickel carbonate,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7707,T3D0686,Nickel carbonate,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7708,T3D0686,Nickel carbonate,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7709,T3D0686,Nickel carbonate,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7710,T3D0686,Nickel carbonate,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7711,T3D0686,Nickel carbonate,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7712,T3D0686,Nickel carbonate,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7713,T3D0686,Nickel carbonate,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7714,T3D0686,Nickel carbonate,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7715,T3D0686,Nickel carbonate,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7716,T3D0686,Nickel carbonate,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7717,T3D0686,Nickel carbonate,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7718,T3D0687,Nickel chloride,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7719,T3D0687,Nickel chloride,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7720,T3D0687,Nickel chloride,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7721,T3D0687,Nickel chloride,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7722,T3D0687,Nickel chloride,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7723,T3D0687,Nickel chloride,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7724,T3D0687,Nickel chloride,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7725,T3D0687,Nickel chloride,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7726,T3D0687,Nickel chloride,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7727,T3D0687,Nickel chloride,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7728,T3D0687,Nickel chloride,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7729,T3D0687,Nickel chloride,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7730,T3D0687,Nickel chloride,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7731,T3D0687,Nickel chloride,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7732,T3D0687,Nickel chloride,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7733,T3D0687,Nickel chloride,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7734,T3D0687,Nickel chloride,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7735,T3D0688,Nickel chromate,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7736,T3D0688,Nickel chromate,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7737,T3D0688,Nickel chromate,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7738,T3D0688,Nickel chromate,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7739,T3D0688,Nickel chromate,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7740,T3D0688,Nickel chromate,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7741,T3D0688,Nickel chromate,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7743,T3D0688,Nickel chromate,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7744,T3D0688,Nickel chromate,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7745,T3D0688,Nickel chromate,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7746,T3D0688,Nickel chromate,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7747,T3D0688,Nickel chromate,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7748,T3D0688,Nickel chromate,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7749,T3D0688,Nickel chromate,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7750,T3D0688,Nickel chromate,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7751,T3D0688,Nickel chromate,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7752,T3D0688,Nickel chromate,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7753,T3D0688,Nickel chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
7754,T3D0688,Nickel chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
7755,T3D0688,Nickel chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
7756,T3D0688,Nickel chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
7757,T3D0688,Nickel chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
7758,T3D0689,Nickel cyanide,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7759,T3D0689,Nickel cyanide,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7760,T3D0689,Nickel cyanide,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7761,T3D0689,Nickel cyanide,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7762,T3D0689,Nickel cyanide,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7763,T3D0689,Nickel cyanide,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7764,T3D0689,Nickel cyanide,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7765,T3D0689,Nickel cyanide,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7766,T3D0689,Nickel cyanide,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7767,T3D0689,Nickel cyanide,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7768,T3D0689,Nickel cyanide,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7769,T3D0689,Nickel cyanide,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7770,T3D0689,Nickel cyanide,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7771,T3D0689,Nickel cyanide,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7772,T3D0689,Nickel cyanide,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7773,T3D0689,Nickel cyanide,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7774,T3D0689,Nickel cyanide,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7775,T3D0689,Nickel cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
7776,T3D0689,Nickel cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
7777,T3D0689,Nickel cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
7778,T3D0689,Nickel cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7779,T3D0689,Nickel cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7780,T3D0689,Nickel cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7781,T3D0689,Nickel cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7782,T3D0689,Nickel cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7783,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7784,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7785,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7786,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7787,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7788,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7789,T3D0689,Nickel cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7790,T3D0689,Nickel cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7791,T3D0689,Nickel cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7792,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7793,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7794,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7795,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7796,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7797,T3D0689,Nickel cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
7798,T3D0689,Nickel cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
7799,T3D0689,Nickel cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
7800,T3D0689,Nickel cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
7801,T3D0689,Nickel cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
7802,T3D0689,Nickel cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
7803,T3D0689,Nickel cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
7804,T3D0689,Nickel cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
7805,T3D0689,Nickel cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
7806,T3D0689,Nickel cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
7807,T3D0689,Nickel cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
7808,T3D0689,Nickel cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
7809,T3D0689,Nickel cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
7810,T3D0689,Nickel cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
7811,T3D0689,Nickel cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
7812,T3D0689,Nickel cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
7813,T3D0689,Nickel cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
7814,T3D0690,Nickel tetracarbonyl,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7815,T3D0690,Nickel tetracarbonyl,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7816,T3D0690,Nickel tetracarbonyl,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7817,T3D0690,Nickel tetracarbonyl,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7819,T3D0690,Nickel tetracarbonyl,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7820,T3D0690,Nickel tetracarbonyl,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7821,T3D0690,Nickel tetracarbonyl,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7822,T3D0690,Nickel tetracarbonyl,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7823,T3D0690,Nickel tetracarbonyl,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7824,T3D0690,Nickel tetracarbonyl,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7825,T3D0690,Nickel tetracarbonyl,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7826,T3D0690,Nickel tetracarbonyl,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7827,T3D0690,Nickel tetracarbonyl,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7828,T3D0690,Nickel tetracarbonyl,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7829,T3D0690,Nickel tetracarbonyl,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7830,T3D0690,Nickel tetracarbonyl,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7831,T3D0690,Nickel tetracarbonyl,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7832,T3D0691,Nickel bromide,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7833,T3D0691,Nickel bromide,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7834,T3D0691,Nickel bromide,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7835,T3D0691,Nickel bromide,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7836,T3D0691,Nickel bromide,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7837,T3D0691,Nickel bromide,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7838,T3D0691,Nickel bromide,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7839,T3D0691,Nickel bromide,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7840,T3D0691,Nickel bromide,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7841,T3D0691,Nickel bromide,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7842,T3D0691,Nickel bromide,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7843,T3D0691,Nickel bromide,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7844,T3D0691,Nickel bromide,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7845,T3D0691,Nickel bromide,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7846,T3D0691,Nickel bromide,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7847,T3D0691,Nickel bromide,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7848,T3D0691,Nickel bromide,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7849,T3D0692,Nickel fluoride,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7850,T3D0692,Nickel fluoride,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7851,T3D0692,Nickel fluoride,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7852,T3D0692,Nickel fluoride,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7853,T3D0692,Nickel fluoride,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7854,T3D0692,Nickel fluoride,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7855,T3D0692,Nickel fluoride,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7856,T3D0692,Nickel fluoride,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7857,T3D0692,Nickel fluoride,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7858,T3D0692,Nickel fluoride,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7859,T3D0692,Nickel fluoride,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7860,T3D0692,Nickel fluoride,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7861,T3D0692,Nickel fluoride,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7862,T3D0692,Nickel fluoride,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7863,T3D0692,Nickel fluoride,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7864,T3D0692,Nickel fluoride,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7865,T3D0692,Nickel fluoride,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7866,T3D0693,Nickel hydroxide,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7867,T3D0693,Nickel hydroxide,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7868,T3D0693,Nickel hydroxide,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7869,T3D0693,Nickel hydroxide,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7870,T3D0693,Nickel hydroxide,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7871,T3D0693,Nickel hydroxide,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7872,T3D0693,Nickel hydroxide,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7873,T3D0693,Nickel hydroxide,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7874,T3D0693,Nickel hydroxide,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7875,T3D0693,Nickel hydroxide,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7876,T3D0693,Nickel hydroxide,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7877,T3D0693,Nickel hydroxide,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7878,T3D0693,Nickel hydroxide,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7879,T3D0693,Nickel hydroxide,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7880,T3D0693,Nickel hydroxide,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7881,T3D0693,Nickel hydroxide,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7882,T3D0693,Nickel hydroxide,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7883,T3D0694,Nickel iodide,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7884,T3D0694,Nickel iodide,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7885,T3D0694,Nickel iodide,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7886,T3D0694,Nickel iodide,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7887,T3D0694,Nickel iodide,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7888,T3D0694,Nickel iodide,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7889,T3D0694,Nickel iodide,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7890,T3D0694,Nickel iodide,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7891,T3D0694,Nickel iodide,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7892,T3D0694,Nickel iodide,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7893,T3D0694,Nickel iodide,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7894,T3D0694,Nickel iodide,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7895,T3D0694,Nickel iodide,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7896,T3D0694,Nickel iodide,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7897,T3D0694,Nickel iodide,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7898,T3D0694,Nickel iodide,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7899,T3D0694,Nickel iodide,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7900,T3D0695,Nickel nitrate,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7901,T3D0695,Nickel nitrate,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7902,T3D0695,Nickel nitrate,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7903,T3D0695,Nickel nitrate,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7904,T3D0695,Nickel nitrate,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7905,T3D0695,Nickel nitrate,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7906,T3D0695,Nickel nitrate,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7907,T3D0695,Nickel nitrate,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7908,T3D0695,Nickel nitrate,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7909,T3D0695,Nickel nitrate,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7911,T3D0695,Nickel nitrate,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7912,T3D0695,Nickel nitrate,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7913,T3D0695,Nickel nitrate,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7914,T3D0695,Nickel nitrate,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7915,T3D0695,Nickel nitrate,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7916,T3D0695,Nickel nitrate,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7917,T3D0695,Nickel nitrate,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7918,T3D0696,Nickel oxide,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7919,T3D0696,Nickel oxide,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7920,T3D0696,Nickel oxide,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7921,T3D0696,Nickel oxide,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7923,T3D0696,Nickel oxide,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7924,T3D0696,Nickel oxide,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7925,T3D0696,Nickel oxide,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7926,T3D0696,Nickel oxide,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7927,T3D0696,Nickel oxide,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7928,T3D0696,Nickel oxide,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7929,T3D0696,Nickel oxide,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7930,T3D0696,Nickel oxide,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7931,T3D0696,Nickel oxide,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7932,T3D0696,Nickel oxide,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7933,T3D0696,Nickel oxide,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7934,T3D0696,Nickel oxide,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7935,T3D0696,Nickel oxide,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7936,T3D0697,Nickel sulfate,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7937,T3D0697,Nickel sulfate,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7938,T3D0697,Nickel sulfate,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7939,T3D0697,Nickel sulfate,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7940,T3D0697,Nickel sulfate,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7941,T3D0697,Nickel sulfate,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7942,T3D0697,Nickel sulfate,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7943,T3D0697,Nickel sulfate,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7944,T3D0697,Nickel sulfate,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7945,T3D0697,Nickel sulfate,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7946,T3D0697,Nickel sulfate,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7947,T3D0697,Nickel sulfate,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7948,T3D0697,Nickel sulfate,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7949,T3D0697,Nickel sulfate,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7950,T3D0697,Nickel sulfate,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7951,T3D0697,Nickel sulfate,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7952,T3D0697,Nickel sulfate,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7953,T3D0698,Nickel subsulfide,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7954,T3D0698,Nickel subsulfide,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7955,T3D0698,Nickel subsulfide,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7956,T3D0698,Nickel subsulfide,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7957,T3D0698,Nickel subsulfide,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7958,T3D0698,Nickel subsulfide,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7959,T3D0698,Nickel subsulfide,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7960,T3D0698,Nickel subsulfide,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7961,T3D0698,Nickel subsulfide,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7962,T3D0698,Nickel subsulfide,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7963,T3D0698,Nickel subsulfide,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7964,T3D0698,Nickel subsulfide,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7965,T3D0698,Nickel subsulfide,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7966,T3D0698,Nickel subsulfide,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7967,T3D0698,Nickel subsulfide,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7968,T3D0698,Nickel subsulfide,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7969,T3D0698,Nickel subsulfide,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7970,T3D0699,Nickel sulfamate,Histone H1.2,P16403,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7971,T3D0699,Nickel sulfamate,Histone H1.3,P16402,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7972,T3D0699,Nickel sulfamate,Histone H1.4,P10412,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7973,T3D0699,Nickel sulfamate,Histone H1.5,P16401,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7974,T3D0699,Nickel sulfamate,Histone H2B type 1-B,P33778,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7975,T3D0699,Nickel sulfamate,Histone H2B type 1-C/E/F/G/I,P62807,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7976,T3D0699,Nickel sulfamate,Histone H2B type 1-D,P58876,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7977,T3D0699,Nickel sulfamate,Histone H2B type 1-L,Q99880,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7978,T3D0699,Nickel sulfamate,Histone H2B type 1-M,Q99879,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7979,T3D0699,Nickel sulfamate,Histone H2B type 1-N,Q99877,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7980,T3D0699,Nickel sulfamate,Histone H3-like centromeric protein A,P49450,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7981,T3D0699,Nickel sulfamate,Histone H3.1,P68431,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7982,T3D0699,Nickel sulfamate,Histone H3.3,P84243,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7983,T3D0699,Nickel sulfamate,Histone H4,P62805,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7984,T3D0699,Nickel sulfamate,Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform,P16298,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7985,T3D0699,Nickel sulfamate,Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform,P48454,"Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. (R100)"
7986,T3D0699,Nickel sulfamate,Sperm protamine-P1,P04553,"Nickel has a high affinity for chromatin proteins, particularly histones and protamines. The complexing of nickel ions with heterochromatin results in a number of alterations including condensation, DNA hypermethylation, gene silencing, and inhibition of histone acetylation, which have been shown to disturb gene expression. (R098)"
7987,T3D0700,Ammonium dichromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
7988,T3D0700,Ammonium dichromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
7989,T3D0700,Ammonium dichromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
7990,T3D0700,Ammonium dichromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
7991,T3D0700,Ammonium dichromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
7992,T3D0701,Barium chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
7993,T3D0701,Barium chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
7994,T3D0701,Barium chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
7995,T3D0701,Barium chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
7996,T3D0701,Barium chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
7997,T3D0701,Barium chromate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
7998,T3D0701,Barium chromate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
7999,T3D0701,Barium chromate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8000,T3D0701,Barium chromate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8001,T3D0701,Barium chromate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8002,T3D0701,Barium chromate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8003,T3D0701,Barium chromate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8004,T3D0701,Barium chromate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
8005,T3D0701,Barium chromate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8006,T3D0701,Barium chromate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8007,T3D0701,Barium chromate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8008,T3D0701,Barium chromate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8009,T3D0701,Barium chromate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8010,T3D0701,Barium chromate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8011,T3D0701,Barium chromate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8012,T3D0701,Barium chromate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
8013,T3D0701,Barium chromate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
8014,T3D0701,Barium chromate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
8015,T3D0701,Barium chromate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
8016,T3D0701,Barium chromate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
8017,T3D0701,Barium chromate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
8018,T3D0702,Caesium chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8019,T3D0702,Caesium chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8020,T3D0702,Caesium chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8021,T3D0702,Caesium chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8022,T3D0702,Caesium chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8028,T3D0704,Iron(III) chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8029,T3D0704,Iron(III) chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8030,T3D0704,Iron(III) chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8031,T3D0704,Iron(III) chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8032,T3D0704,Iron(III) chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8033,T3D0705,Potassium chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8034,T3D0705,Potassium chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8035,T3D0705,Potassium chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8036,T3D0705,Potassium chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8037,T3D0705,Potassium chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8038,T3D0706,Potassium dichromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8039,T3D0706,Potassium dichromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8040,T3D0706,Potassium dichromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8041,T3D0706,Potassium dichromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8042,T3D0706,Potassium dichromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8043,T3D0707,Pyridinium chlorochromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8044,T3D0707,Pyridinium chlorochromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8045,T3D0707,Pyridinium chlorochromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8046,T3D0707,Pyridinium chlorochromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8047,T3D0707,Pyridinium chlorochromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8048,T3D0708,Pyridinium dichromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8049,T3D0708,Pyridinium dichromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8050,T3D0708,Pyridinium dichromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8051,T3D0708,Pyridinium dichromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8052,T3D0708,Pyridinium dichromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8053,T3D0709,Silver chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8054,T3D0709,Silver chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8055,T3D0709,Silver chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8056,T3D0709,Silver chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8057,T3D0709,Silver chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8058,T3D0709,Silver chromate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
8059,T3D0709,Silver chromate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
8060,T3D0709,Silver chromate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
8061,T3D0709,Silver chromate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
8062,T3D0709,Silver chromate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
8063,T3D0709,Silver chromate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
8064,T3D0709,Silver chromate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
8065,T3D0709,Silver chromate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
8066,T3D0709,Silver chromate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8067,T3D0709,Silver chromate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8068,T3D0709,Silver chromate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8069,T3D0709,Silver chromate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8070,T3D0709,Silver chromate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8071,T3D0709,Silver chromate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8072,T3D0709,Silver chromate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8073,T3D0709,Silver chromate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8074,T3D0710,Sodium chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8075,T3D0710,Sodium chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8076,T3D0710,Sodium chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8077,T3D0710,Sodium chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8078,T3D0710,Sodium chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8079,T3D0711,Sodium dichromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8080,T3D0711,Sodium dichromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8081,T3D0711,Sodium dichromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8082,T3D0711,Sodium dichromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8083,T3D0711,Sodium dichromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8084,T3D0712,Strontium chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8085,T3D0712,Strontium chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8086,T3D0712,Strontium chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8087,T3D0712,Strontium chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8088,T3D0712,Strontium chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8089,T3D0713,Zinc chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8090,T3D0713,Zinc chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8091,T3D0713,Zinc chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8092,T3D0713,Zinc chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8093,T3D0713,Zinc chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8094,T3D0713,Zinc chromate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
8095,T3D0714,Ammonium chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8096,T3D0714,Ammonium chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8097,T3D0714,Ammonium chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8098,T3D0714,Ammonium chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8099,T3D0714,Ammonium chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8100,T3D0715,Lithuim chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8101,T3D0715,Lithuim chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8102,T3D0715,Lithuim chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8103,T3D0715,Lithuim chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8104,T3D0715,Lithuim chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8105,T3D0716,Zinc dichromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8106,T3D0716,Zinc dichromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8107,T3D0716,Zinc dichromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8108,T3D0716,Zinc dichromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8109,T3D0716,Zinc dichromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8110,T3D0716,Zinc dichromate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
8111,T3D0717,Lead chromate oxide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8112,T3D0717,Lead chromate oxide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8113,T3D0717,Lead chromate oxide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8114,T3D0717,Lead chromate oxide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8115,T3D0717,Lead chromate oxide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8116,T3D0717,Lead chromate oxide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
8117,T3D0717,Lead chromate oxide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
8118,T3D0717,Lead chromate oxide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
8119,T3D0717,Lead chromate oxide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
8120,T3D0717,Lead chromate oxide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8121,T3D0717,Lead chromate oxide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8122,T3D0717,Lead chromate oxide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8123,T3D0717,Lead chromate oxide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8124,T3D0717,Lead chromate oxide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8125,T3D0717,Lead chromate oxide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8126,T3D0717,Lead chromate oxide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8127,T3D0717,Lead chromate oxide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8128,T3D0717,Lead chromate oxide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8129,T3D0717,Lead chromate oxide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8130,T3D0717,Lead chromate oxide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8131,T3D0717,Lead chromate oxide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8132,T3D0717,Lead chromate oxide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8133,T3D0717,Lead chromate oxide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8134,T3D0717,Lead chromate oxide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8135,T3D0717,Lead chromate oxide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8136,T3D0717,Lead chromate oxide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
8137,T3D0717,Lead chromate oxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
8138,T3D0717,Lead chromate oxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
8139,T3D0717,Lead chromate oxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
8140,T3D0717,Lead chromate oxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
8141,T3D0717,Lead chromate oxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
8142,T3D0717,Lead chromate oxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
8143,T3D0717,Lead chromate oxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
8144,T3D0717,Lead chromate oxide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
8145,T3D0718,Zinc potassium chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8146,T3D0718,Zinc potassium chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8147,T3D0718,Zinc potassium chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8148,T3D0718,Zinc potassium chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8149,T3D0718,Zinc potassium chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8150,T3D0719,Zinc chromate hydroxide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8151,T3D0719,Zinc chromate hydroxide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
8152,T3D0719,Zinc chromate hydroxide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
8153,T3D0719,Zinc chromate hydroxide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8154,T3D0719,Zinc chromate hydroxide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
8155,T3D0719,Zinc chromate hydroxide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
8156,T3D0215,Chromic acid,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
8158,T3D0720,Zinc acetate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
8159,T3D0722,Zinc arsenide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
8160,T3D0722,Zinc arsenide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
8161,T3D0722,Zinc arsenide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
8162,T3D0722,Zinc arsenide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
8163,T3D0722,Zinc arsenide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
8164,T3D0722,Zinc arsenide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
8165,T3D0722,Zinc arsenide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
8166,T3D0722,Zinc arsenide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
8167,T3D0722,Zinc arsenide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
8168,T3D0722,Zinc arsenide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
8169,T3D0722,Zinc arsenide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
8170,T3D0722,Zinc arsenide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
8171,T3D0722,Zinc arsenide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
8172,T3D0722,Zinc arsenide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
8173,T3D0722,Zinc arsenide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
8174,T3D0722,Zinc arsenide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
8175,T3D0722,Zinc arsenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8176,T3D0722,Zinc arsenide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8177,T3D0722,Zinc arsenide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8178,T3D0722,Zinc arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
8179,T3D0722,Zinc arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
8180,T3D0722,Zinc arsenide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
8181,T3D0722,Zinc arsenide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
8182,T3D0722,Zinc arsenide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
8183,T3D0722,Zinc arsenide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
8184,T3D0722,Zinc arsenide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
8185,T3D0722,Zinc arsenide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8186,T3D0722,Zinc arsenide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8187,T3D0722,Zinc arsenide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8188,T3D0722,Zinc arsenide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8189,T3D0722,Zinc arsenide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8190,T3D0722,Zinc arsenide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8191,T3D0722,Zinc arsenide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8192,T3D0722,Zinc arsenide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8193,T3D0722,Zinc arsenide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8194,T3D0722,Zinc arsenide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8195,T3D0722,Zinc arsenide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8196,T3D0722,Zinc arsenide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8197,T3D0722,Zinc arsenide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8198,T3D0722,Zinc arsenide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8199,T3D0722,Zinc arsenide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8200,T3D0722,Zinc arsenide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8201,T3D0722,Zinc arsenide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8202,T3D0722,Zinc arsenide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
8203,T3D0727,Zinc cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8204,T3D0727,Zinc cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8205,T3D0727,Zinc cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8206,T3D0727,Zinc cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8207,T3D0727,Zinc cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8208,T3D0727,Zinc cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8209,T3D0727,Zinc cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8210,T3D0727,Zinc cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8211,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8212,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8213,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8214,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8215,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8216,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8217,T3D0727,Zinc cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8218,T3D0727,Zinc cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8219,T3D0727,Zinc cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8220,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8221,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8222,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8223,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8224,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8225,T3D0727,Zinc cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8226,T3D0727,Zinc cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
8227,T3D0727,Zinc cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8228,T3D0727,Zinc cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8229,T3D0727,Zinc cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8230,T3D0727,Zinc cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8231,T3D0727,Zinc cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8232,T3D0727,Zinc cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
8233,T3D0727,Zinc cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8234,T3D0727,Zinc cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8235,T3D0727,Zinc cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
8236,T3D0727,Zinc cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
8237,T3D0727,Zinc cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
8238,T3D0727,Zinc cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8239,T3D0727,Zinc cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8240,T3D0727,Zinc cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8241,T3D0727,Zinc cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8242,T3D0753,Copper(I) cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8243,T3D0753,Copper(I) cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8244,T3D0753,Copper(I) cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8245,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8246,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8247,T3D0753,Copper(I) cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8248,T3D0753,Copper(I) cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8249,T3D0753,Copper(I) cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8250,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8251,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8252,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8253,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8254,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8255,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8256,T3D0753,Copper(I) cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8257,T3D0753,Copper(I) cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8258,T3D0753,Copper(I) cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8259,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8260,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8261,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8262,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8263,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8264,T3D0753,Copper(I) cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8265,T3D0753,Copper(I) cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
8266,T3D0753,Copper(I) cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8267,T3D0753,Copper(I) cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8268,T3D0753,Copper(I) cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8269,T3D0753,Copper(I) cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8270,T3D0753,Copper(I) cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8271,T3D0753,Copper(I) cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
8272,T3D0753,Copper(I) cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8273,T3D0753,Copper(I) cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8274,T3D0753,Copper(I) cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
8275,T3D0753,Copper(I) cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
8276,T3D0753,Copper(I) cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
8277,T3D0753,Copper(I) cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8278,T3D0753,Copper(I) cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8279,T3D0753,Copper(I) cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8280,T3D0753,Copper(I) cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8281,T3D0753,Copper(I) cyanide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
8282,T3D0753,Copper(I) cyanide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
8283,T3D0753,Copper(I) cyanide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
8284,T3D0753,Copper(I) cyanide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
8285,T3D0753,Copper(I) cyanide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
8286,T3D0754,Cyanogen,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8287,T3D0754,Cyanogen,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8288,T3D0754,Cyanogen,Catalase,P04040,Cyanide inhibits catalase. (R211)
8289,T3D0754,Cyanogen,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8290,T3D0754,Cyanogen,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8291,T3D0754,Cyanogen,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8292,T3D0754,Cyanogen,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8293,T3D0754,Cyanogen,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8294,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8295,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8296,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8297,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8298,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8299,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8300,T3D0754,Cyanogen,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8301,T3D0754,Cyanogen,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8302,T3D0754,Cyanogen,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8303,T3D0754,Cyanogen,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8304,T3D0754,Cyanogen,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8305,T3D0754,Cyanogen,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8306,T3D0754,Cyanogen,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8308,T3D0754,Cyanogen,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8309,T3D0754,Cyanogen,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8310,T3D0754,Cyanogen,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8311,T3D0754,Cyanogen,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8312,T3D0755,Cyanogen bromide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8313,T3D0755,Cyanogen bromide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8314,T3D0755,Cyanogen bromide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8315,T3D0755,Cyanogen bromide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8316,T3D0755,Cyanogen bromide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8317,T3D0755,Cyanogen bromide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8318,T3D0755,Cyanogen bromide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8319,T3D0755,Cyanogen bromide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8320,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8321,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8322,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8323,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8324,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8325,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8326,T3D0755,Cyanogen bromide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8327,T3D0755,Cyanogen bromide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8328,T3D0755,Cyanogen bromide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8329,T3D0755,Cyanogen bromide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8330,T3D0755,Cyanogen bromide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8331,T3D0755,Cyanogen bromide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8332,T3D0755,Cyanogen bromide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8333,T3D0755,Cyanogen bromide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8334,T3D0755,Cyanogen bromide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8335,T3D0755,Cyanogen bromide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8336,T3D0755,Cyanogen bromide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8337,T3D0756,Cyanogen chloride,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8338,T3D0756,Cyanogen chloride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8339,T3D0756,Cyanogen chloride,Catalase,P04040,Cyanide inhibits catalase. (R211)
8340,T3D0756,Cyanogen chloride,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8341,T3D0756,Cyanogen chloride,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8342,T3D0756,Cyanogen chloride,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8343,T3D0756,Cyanogen chloride,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8344,T3D0756,Cyanogen chloride,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8345,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8346,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8347,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8348,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8349,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8350,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8351,T3D0756,Cyanogen chloride,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8352,T3D0756,Cyanogen chloride,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8353,T3D0756,Cyanogen chloride,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8354,T3D0756,Cyanogen chloride,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8355,T3D0756,Cyanogen chloride,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8356,T3D0756,Cyanogen chloride,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8357,T3D0756,Cyanogen chloride,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8358,T3D0756,Cyanogen chloride,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8359,T3D0756,Cyanogen chloride,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8360,T3D0756,Cyanogen chloride,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8361,T3D0756,Cyanogen chloride,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8362,T3D0758,Cyanogen iodide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8363,T3D0758,Cyanogen iodide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8364,T3D0758,Cyanogen iodide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8365,T3D0758,Cyanogen iodide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8366,T3D0758,Cyanogen iodide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8367,T3D0758,Cyanogen iodide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8368,T3D0758,Cyanogen iodide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8369,T3D0758,Cyanogen iodide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8370,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8371,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8372,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8373,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8374,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8375,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8376,T3D0758,Cyanogen iodide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8377,T3D0758,Cyanogen iodide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8378,T3D0758,Cyanogen iodide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8379,T3D0758,Cyanogen iodide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8380,T3D0758,Cyanogen iodide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8381,T3D0758,Cyanogen iodide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8382,T3D0758,Cyanogen iodide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8383,T3D0758,Cyanogen iodide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8384,T3D0758,Cyanogen iodide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8385,T3D0758,Cyanogen iodide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8386,T3D0758,Cyanogen iodide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8387,T3D0759,Calcium cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8388,T3D0759,Calcium cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8389,T3D0759,Calcium cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8390,T3D0759,Calcium cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8391,T3D0759,Calcium cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8392,T3D0759,Calcium cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8393,T3D0759,Calcium cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8394,T3D0759,Calcium cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8395,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8396,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8397,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8398,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8399,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8400,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8401,T3D0759,Calcium cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8402,T3D0759,Calcium cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8403,T3D0759,Calcium cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8404,T3D0759,Calcium cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8405,T3D0759,Calcium cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8406,T3D0759,Calcium cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8407,T3D0759,Calcium cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8408,T3D0759,Calcium cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8409,T3D0759,Calcium cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8410,T3D0759,Calcium cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8411,T3D0759,Calcium cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8412,T3D0760,Ammonium thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8413,T3D0760,Ammonium thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8414,T3D0760,Ammonium thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8415,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8416,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8417,T3D0760,Ammonium thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8418,T3D0760,Ammonium thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8419,T3D0760,Ammonium thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8420,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8421,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8422,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8423,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8424,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8425,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8426,T3D0760,Ammonium thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8427,T3D0760,Ammonium thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8428,T3D0760,Ammonium thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8429,T3D0760,Ammonium thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8430,T3D0760,Ammonium thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8431,T3D0760,Ammonium thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8432,T3D0760,Ammonium thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8433,T3D0760,Ammonium thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8434,T3D0760,Ammonium thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8435,T3D0760,Ammonium thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8436,T3D0760,Ammonium thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8437,T3D0761,Potassium cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8438,T3D0761,Potassium cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8439,T3D0761,Potassium cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8440,T3D0761,Potassium cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8441,T3D0761,Potassium cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8442,T3D0761,Potassium cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8443,T3D0761,Potassium cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8444,T3D0761,Potassium cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8445,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8446,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8447,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8448,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8449,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8450,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8451,T3D0761,Potassium cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8452,T3D0761,Potassium cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8453,T3D0761,Potassium cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8454,T3D0761,Potassium cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8455,T3D0761,Potassium cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8456,T3D0761,Potassium cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8457,T3D0761,Potassium cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8458,T3D0761,Potassium cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8459,T3D0761,Potassium cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8460,T3D0761,Potassium cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8461,T3D0761,Potassium cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8462,T3D0762,Potassium ferricyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8463,T3D0762,Potassium ferricyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8464,T3D0762,Potassium ferricyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8465,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8466,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8467,T3D0762,Potassium ferricyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8468,T3D0762,Potassium ferricyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8469,T3D0762,Potassium ferricyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8470,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8471,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8472,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8473,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8474,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8475,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8476,T3D0762,Potassium ferricyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8477,T3D0762,Potassium ferricyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8478,T3D0762,Potassium ferricyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8479,T3D0762,Potassium ferricyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8480,T3D0762,Potassium ferricyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8481,T3D0762,Potassium ferricyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8482,T3D0762,Potassium ferricyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8483,T3D0762,Potassium ferricyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8484,T3D0762,Potassium ferricyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8485,T3D0762,Potassium ferricyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8486,T3D0762,Potassium ferricyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8487,T3D0763,Potassium ferrocyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8488,T3D0763,Potassium ferrocyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8489,T3D0763,Potassium ferrocyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8490,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8491,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8492,T3D0763,Potassium ferrocyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8493,T3D0763,Potassium ferrocyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8494,T3D0763,Potassium ferrocyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8495,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8496,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8497,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8498,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8499,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8500,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8501,T3D0763,Potassium ferrocyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8502,T3D0763,Potassium ferrocyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8503,T3D0763,Potassium ferrocyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8504,T3D0763,Potassium ferrocyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8505,T3D0763,Potassium ferrocyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8506,T3D0763,Potassium ferrocyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8507,T3D0763,Potassium ferrocyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8508,T3D0763,Potassium ferrocyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8509,T3D0763,Potassium ferrocyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8510,T3D0763,Potassium ferrocyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8511,T3D0763,Potassium ferrocyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8512,T3D0764,Potassium silver cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8513,T3D0764,Potassium silver cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8514,T3D0764,Potassium silver cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8515,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8516,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8517,T3D0764,Potassium silver cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8518,T3D0764,Potassium silver cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8519,T3D0764,Potassium silver cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8520,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8521,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8522,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8523,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8524,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8525,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8526,T3D0764,Potassium silver cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8527,T3D0764,Potassium silver cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8528,T3D0764,Potassium silver cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8529,T3D0764,Potassium silver cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8530,T3D0764,Potassium silver cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8531,T3D0764,Potassium silver cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8532,T3D0764,Potassium silver cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8533,T3D0764,Potassium silver cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8534,T3D0764,Potassium silver cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8535,T3D0764,Potassium silver cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8536,T3D0764,Potassium silver cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8537,T3D0764,Potassium silver cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
8538,T3D0764,Potassium silver cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
8539,T3D0764,Potassium silver cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
8540,T3D0764,Potassium silver cyanide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8541,T3D0764,Potassium silver cyanide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8542,T3D0764,Potassium silver cyanide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8543,T3D0764,Potassium silver cyanide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8544,T3D0764,Potassium silver cyanide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8545,T3D0764,Potassium silver cyanide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8546,T3D0764,Potassium silver cyanide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8547,T3D0764,Potassium silver cyanide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8548,T3D0765,Silver cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8549,T3D0765,Silver cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8550,T3D0765,Silver cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8551,T3D0765,Silver cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8552,T3D0765,Silver cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8553,T3D0765,Silver cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8554,T3D0765,Silver cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8555,T3D0765,Silver cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8556,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8557,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8558,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8559,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8560,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8561,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8562,T3D0765,Silver cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8563,T3D0765,Silver cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8564,T3D0765,Silver cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8565,T3D0765,Silver cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8566,T3D0765,Silver cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8567,T3D0765,Silver cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8568,T3D0765,Silver cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8569,T3D0765,Silver cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8570,T3D0765,Silver cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8571,T3D0765,Silver cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8572,T3D0765,Silver cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8573,T3D0765,Silver cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
8574,T3D0765,Silver cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
8575,T3D0765,Silver cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
8576,T3D0765,Silver cyanide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8577,T3D0765,Silver cyanide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8578,T3D0765,Silver cyanide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8579,T3D0765,Silver cyanide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8580,T3D0765,Silver cyanide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8581,T3D0765,Silver cyanide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8582,T3D0765,Silver cyanide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8583,T3D0765,Silver cyanide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
8584,T3D0766,Sodium cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8585,T3D0766,Sodium cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8586,T3D0766,Sodium cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8587,T3D0766,Sodium cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8588,T3D0766,Sodium cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8589,T3D0766,Sodium cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8590,T3D0766,Sodium cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8591,T3D0766,Sodium cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8592,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8593,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8594,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8595,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8596,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8597,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8598,T3D0766,Sodium cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8599,T3D0766,Sodium cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8600,T3D0766,Sodium cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8601,T3D0766,Sodium cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8602,T3D0766,Sodium cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8603,T3D0766,Sodium cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8604,T3D0766,Sodium cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8605,T3D0766,Sodium cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8606,T3D0766,Sodium cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8607,T3D0766,Sodium cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8608,T3D0766,Sodium cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8609,T3D0767,Sodium ferrocyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8610,T3D0767,Sodium ferrocyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8611,T3D0767,Sodium ferrocyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8612,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8613,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8614,T3D0767,Sodium ferrocyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8615,T3D0767,Sodium ferrocyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8616,T3D0767,Sodium ferrocyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8617,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8618,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8619,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8620,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8622,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8623,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8624,T3D0767,Sodium ferrocyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8625,T3D0767,Sodium ferrocyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8626,T3D0767,Sodium ferrocyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8627,T3D0767,Sodium ferrocyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8628,T3D0767,Sodium ferrocyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8629,T3D0767,Sodium ferrocyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8630,T3D0767,Sodium ferrocyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8631,T3D0767,Sodium ferrocyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8632,T3D0767,Sodium ferrocyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8633,T3D0767,Sodium ferrocyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8634,T3D0767,Sodium ferrocyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8635,T3D0768,Sodium nitroprusside,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8636,T3D0768,Sodium nitroprusside,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8637,T3D0768,Sodium nitroprusside,Catalase,P04040,Cyanide inhibits catalase. (R211)
8638,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8639,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8640,T3D0768,Sodium nitroprusside,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8641,T3D0768,Sodium nitroprusside,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8642,T3D0768,Sodium nitroprusside,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8643,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8644,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8645,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8646,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8647,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8648,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8649,T3D0768,Sodium nitroprusside,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8650,T3D0768,Sodium nitroprusside,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8651,T3D0768,Sodium nitroprusside,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8652,T3D0768,Sodium nitroprusside,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8653,T3D0768,Sodium nitroprusside,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8654,T3D0768,Sodium nitroprusside,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8655,T3D0768,Sodium nitroprusside,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8656,T3D0768,Sodium nitroprusside,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8657,T3D0768,Sodium nitroprusside,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8658,T3D0768,Sodium nitroprusside,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8659,T3D0768,Sodium nitroprusside,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8660,T3D0769,Trimethylsilyl cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8661,T3D0769,Trimethylsilyl cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8662,T3D0769,Trimethylsilyl cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
8663,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8664,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8665,T3D0769,Trimethylsilyl cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8666,T3D0769,Trimethylsilyl cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8667,T3D0769,Trimethylsilyl cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8668,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8669,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8670,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8671,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8672,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8673,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8674,T3D0769,Trimethylsilyl cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8675,T3D0769,Trimethylsilyl cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8676,T3D0769,Trimethylsilyl cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8677,T3D0769,Trimethylsilyl cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8678,T3D0769,Trimethylsilyl cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8679,T3D0769,Trimethylsilyl cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8680,T3D0769,Trimethylsilyl cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8681,T3D0769,Trimethylsilyl cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8682,T3D0769,Trimethylsilyl cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8683,T3D0769,Trimethylsilyl cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8684,T3D0769,Trimethylsilyl cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8685,T3D0776,Potassium cyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8686,T3D0776,Potassium cyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8687,T3D0776,Potassium cyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8688,T3D0776,Potassium cyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8689,T3D0776,Potassium cyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8690,T3D0776,Potassium cyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8691,T3D0776,Potassium cyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8692,T3D0776,Potassium cyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8693,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8694,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8695,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8696,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8697,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8698,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8699,T3D0776,Potassium cyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8700,T3D0776,Potassium cyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8701,T3D0776,Potassium cyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8702,T3D0776,Potassium cyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8703,T3D0776,Potassium cyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8704,T3D0776,Potassium cyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8705,T3D0776,Potassium cyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8706,T3D0776,Potassium cyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8707,T3D0776,Potassium cyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8708,T3D0776,Potassium cyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8709,T3D0776,Potassium cyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8710,T3D0777,Isocyanic acid,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8711,T3D0777,Isocyanic acid,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8712,T3D0777,Isocyanic acid,Catalase,P04040,Cyanide inhibits catalase. (R211)
8713,T3D0777,Isocyanic acid,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8714,T3D0777,Isocyanic acid,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8715,T3D0777,Isocyanic acid,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8716,T3D0777,Isocyanic acid,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8717,T3D0777,Isocyanic acid,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8718,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8719,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8720,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8721,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8722,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8723,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8724,T3D0777,Isocyanic acid,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8725,T3D0777,Isocyanic acid,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8726,T3D0777,Isocyanic acid,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8727,T3D0777,Isocyanic acid,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8728,T3D0777,Isocyanic acid,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8729,T3D0777,Isocyanic acid,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8730,T3D0777,Isocyanic acid,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8731,T3D0777,Isocyanic acid,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8732,T3D0777,Isocyanic acid,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8733,T3D0777,Isocyanic acid,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8734,T3D0777,Isocyanic acid,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8735,T3D0778,Allyl isothiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8736,T3D0778,Allyl isothiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8737,T3D0778,Allyl isothiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8738,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8739,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8740,T3D0778,Allyl isothiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8741,T3D0778,Allyl isothiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8742,T3D0778,Allyl isothiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8743,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8744,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8745,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8746,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8747,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8748,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8749,T3D0778,Allyl isothiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8750,T3D0778,Allyl isothiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8751,T3D0778,Allyl isothiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8752,T3D0778,Allyl isothiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8753,T3D0778,Allyl isothiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8754,T3D0778,Allyl isothiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8755,T3D0778,Allyl isothiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8756,T3D0778,Allyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8757,T3D0778,Allyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8758,T3D0778,Allyl isothiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8759,T3D0778,Allyl isothiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8760,T3D0780,Methyl isothiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8761,T3D0780,Methyl isothiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8762,T3D0780,Methyl isothiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8763,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8764,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8765,T3D0780,Methyl isothiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8766,T3D0780,Methyl isothiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8767,T3D0780,Methyl isothiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8768,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8769,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8770,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8771,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8772,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8773,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8774,T3D0780,Methyl isothiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8775,T3D0780,Methyl isothiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8776,T3D0780,Methyl isothiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8777,T3D0780,Methyl isothiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8778,T3D0780,Methyl isothiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8779,T3D0780,Methyl isothiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8780,T3D0780,Methyl isothiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8781,T3D0780,Methyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8782,T3D0780,Methyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8783,T3D0780,Methyl isothiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8784,T3D0780,Methyl isothiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8785,T3D0781,Phenyl isothiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8786,T3D0781,Phenyl isothiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8787,T3D0781,Phenyl isothiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8788,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8789,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8790,T3D0781,Phenyl isothiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8791,T3D0781,Phenyl isothiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8792,T3D0781,Phenyl isothiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8793,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8794,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8795,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8796,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8797,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8798,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8799,T3D0781,Phenyl isothiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8800,T3D0781,Phenyl isothiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8801,T3D0781,Phenyl isothiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8802,T3D0781,Phenyl isothiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8803,T3D0781,Phenyl isothiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8804,T3D0781,Phenyl isothiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8805,T3D0781,Phenyl isothiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8806,T3D0781,Phenyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8807,T3D0781,Phenyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8808,T3D0781,Phenyl isothiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8809,T3D0781,Phenyl isothiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8810,T3D0785,Guanidinium thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8811,T3D0785,Guanidinium thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8812,T3D0785,Guanidinium thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8813,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8814,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8815,T3D0785,Guanidinium thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8816,T3D0785,Guanidinium thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8817,T3D0785,Guanidinium thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8818,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8819,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8820,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8821,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8822,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8823,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8824,T3D0785,Guanidinium thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8825,T3D0785,Guanidinium thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8826,T3D0785,Guanidinium thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8827,T3D0785,Guanidinium thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8828,T3D0785,Guanidinium thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8829,T3D0785,Guanidinium thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8830,T3D0785,Guanidinium thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8831,T3D0785,Guanidinium thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8832,T3D0785,Guanidinium thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8833,T3D0785,Guanidinium thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8834,T3D0785,Guanidinium thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8835,T3D0786,Lead thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8836,T3D0786,Lead thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8837,T3D0786,Lead thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8838,T3D0786,Lead thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8839,T3D0786,Lead thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8840,T3D0786,Lead thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8841,T3D0786,Lead thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8842,T3D0786,Lead thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8843,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8844,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8845,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8846,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8847,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8848,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8849,T3D0786,Lead thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8850,T3D0786,Lead thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8851,T3D0786,Lead thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8852,T3D0786,Lead thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8853,T3D0786,Lead thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8854,T3D0786,Lead thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8855,T3D0786,Lead thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8856,T3D0786,Lead thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8857,T3D0786,Lead thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8858,T3D0786,Lead thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8859,T3D0786,Lead thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8860,T3D0786,Lead thiocyanate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
8861,T3D0786,Lead thiocyanate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
8862,T3D0786,Lead thiocyanate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
8863,T3D0786,Lead thiocyanate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
8864,T3D0786,Lead thiocyanate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8865,T3D0786,Lead thiocyanate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8866,T3D0786,Lead thiocyanate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8867,T3D0786,Lead thiocyanate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8868,T3D0786,Lead thiocyanate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8869,T3D0786,Lead thiocyanate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8870,T3D0786,Lead thiocyanate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
8871,T3D0786,Lead thiocyanate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8872,T3D0786,Lead thiocyanate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8873,T3D0786,Lead thiocyanate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8874,T3D0786,Lead thiocyanate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8875,T3D0786,Lead thiocyanate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8876,T3D0786,Lead thiocyanate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8877,T3D0786,Lead thiocyanate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8878,T3D0786,Lead thiocyanate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8879,T3D0786,Lead thiocyanate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
8880,T3D0786,Lead thiocyanate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
8881,T3D0786,Lead thiocyanate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
8882,T3D0786,Lead thiocyanate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
8883,T3D0786,Lead thiocyanate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
8884,T3D0786,Lead thiocyanate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
8885,T3D0786,Lead thiocyanate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
8886,T3D0786,Lead thiocyanate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
8887,T3D0786,Lead thiocyanate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
8888,T3D0786,Lead thiocyanate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
8889,T3D0787,Potassium thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8890,T3D0787,Potassium thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8891,T3D0787,Potassium thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8892,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8893,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8894,T3D0787,Potassium thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8895,T3D0787,Potassium thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8896,T3D0787,Potassium thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8897,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8898,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8899,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8900,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8901,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8902,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8903,T3D0787,Potassium thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8904,T3D0787,Potassium thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8905,T3D0787,Potassium thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8906,T3D0787,Potassium thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8907,T3D0787,Potassium thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8908,T3D0787,Potassium thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8909,T3D0787,Potassium thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8910,T3D0787,Potassium thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8911,T3D0787,Potassium thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8912,T3D0787,Potassium thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8913,T3D0787,Potassium thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8914,T3D0788,Sodium thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8915,T3D0788,Sodium thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8916,T3D0788,Sodium thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
8917,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8918,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8919,T3D0788,Sodium thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8920,T3D0788,Sodium thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8921,T3D0788,Sodium thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8922,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8923,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8924,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8925,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8926,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8927,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8928,T3D0788,Sodium thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8929,T3D0788,Sodium thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8930,T3D0788,Sodium thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8931,T3D0788,Sodium thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8932,T3D0788,Sodium thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8933,T3D0788,Sodium thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8934,T3D0788,Sodium thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8935,T3D0788,Sodium thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8936,T3D0788,Sodium thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8937,T3D0788,Sodium thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8938,T3D0788,Sodium thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8939,T3D0789,Thiocyanic acid,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8940,T3D0789,Thiocyanic acid,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8941,T3D0789,Thiocyanic acid,Catalase,P04040,Cyanide inhibits catalase. (R211)
8942,T3D0789,Thiocyanic acid,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8943,T3D0789,Thiocyanic acid,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8944,T3D0789,Thiocyanic acid,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8945,T3D0789,Thiocyanic acid,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8946,T3D0789,Thiocyanic acid,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8947,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8948,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8949,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8950,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8951,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8952,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8953,T3D0789,Thiocyanic acid,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8954,T3D0789,Thiocyanic acid,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8955,T3D0789,Thiocyanic acid,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8956,T3D0789,Thiocyanic acid,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8957,T3D0789,Thiocyanic acid,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8958,T3D0789,Thiocyanic acid,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8959,T3D0789,Thiocyanic acid,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8960,T3D0789,Thiocyanic acid,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8961,T3D0789,Thiocyanic acid,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8962,T3D0789,Thiocyanic acid,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8963,T3D0789,Thiocyanic acid,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
8964,T3D0790,Cyanuric acid,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
8965,T3D0790,Cyanuric acid,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
8966,T3D0790,Cyanuric acid,Catalase,P04040,Cyanide inhibits catalase. (R211)
8967,T3D0790,Cyanuric acid,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8968,T3D0790,Cyanuric acid,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8969,T3D0790,Cyanuric acid,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8970,T3D0790,Cyanuric acid,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8971,T3D0790,Cyanuric acid,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8972,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8973,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8974,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8975,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8976,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8977,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
8978,T3D0790,Cyanuric acid,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8979,T3D0790,Cyanuric acid,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
8980,T3D0790,Cyanuric acid,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
8981,T3D0790,Cyanuric acid,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
8982,T3D0790,Cyanuric acid,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
8983,T3D0790,Cyanuric acid,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
8984,T3D0790,Cyanuric acid,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
8985,T3D0790,Cyanuric acid,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
8986,T3D0790,Cyanuric acid,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
8987,T3D0790,Cyanuric acid,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
8988,T3D0790,Cyanuric acid,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
16732,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",DNA,DNA,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. One metabolite in particular, N-hydroxy-N,N’-diacetyl MBOCA, is known to bind nucleic acids, forming DNA adducts. (S193) "
16733,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Serum albumin,P02768,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. (S193) "
16734,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit alpha,P69905,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16735,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit beta,P68871,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16736,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit delta,P02042,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16737,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit epsilon,P02100,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16738,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit gamma-1,P69891,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16739,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit gamma-2,P69892,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16740,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit mu,Q6B0K9,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16741,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit theta-1,P09105,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16742,T3D0152,"4,4'-Methylenebis(2-chloroaniline)",Hemoglobin subunit zeta,P02008,"MBOCA's carcinogenicity is thought to be a result of its ability to bind to DNA, hemoglobin, and serum albumin. N-oxidized MBOCA metabolites, such as n-hydroxy MBOCA and mononitroso-MBOCA, have been shown to form hemoglobin adducts. (S193) "
16743,T3D0721,Zinc antimonide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16744,T3D0722,Zinc arsenide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16745,T3D0723,Zinc bromide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16746,T3D0724,Zinc chlorate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16747,T3D0725,Zinc carbonate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16748,T3D0726,Zinc chloride,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16749,T3D0728,Zinc fluoride,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16750,T3D0729,Zinc gluconate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16751,T3D0730,Zinc hydride,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16752,T3D0731,Zinc hydroxide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16753,T3D0732,Zinc hydrosulfite,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16754,T3D0733,Zinc iodide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16755,T3D0734,Zinc molybdate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16756,T3D0735,Zinc nitrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16757,T3D0736,Zinc oxide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16758,T3D0737,Zinc peroxide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16759,T3D0738,Zinc phosphate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16760,T3D0739,Zinc phosphide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16761,T3D0740,Zinc pyrithione,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16762,T3D0741,Zinc pyrophosphate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16763,T3D0742,Zinc selenide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16764,T3D0743,Zinc stearate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16765,T3D0744,Zinc sulfate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16766,T3D0745,Zinc sulfide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16767,T3D0746,Zinc thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
16768,T3D0747,Zinc silicofluoride,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16769,T3D0748,Diethylzinc,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16770,T3D0749,Dimethylzinc,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16771,T3D0299,Zinc arsenate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16772,T3D0718,Zinc potassium chromate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16773,T3D1156,Zinc permanganate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16774,T3D1183,Uranyl zinc acetate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16775,T3D1373,Zinc cadmium sulfide,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16776,T3D1376,Zinc beryllium silicate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16777,T3D1459,Zinc arsenite,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16778,T3D1460,Zinc diethyldithiocarbamate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16779,T3D1461,Zinc laurate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16780,T3D1462,Zinc oleate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16781,T3D1463,Zinc phenolsulfate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16782,T3D1464,Zinc silicate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16783,T3D1465,Zinc dimethyldithiocarbamate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16784,T3D1466,Zineb,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16785,T3D1467,Diisopropylzinc,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16786,T3D1468,Nysted reagent,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16787,T3D1469,Sodium zincate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16788,T3D1470,Zinc ammonium chloride,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16789,T3D1471,Zinc dithiophosphate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16790,T3D1472,Zinc nitride,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16791,T3D1473,Zinc trifluoromethanesulfonate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16792,T3D1474,Zinc borate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16793,T3D1475,Zinc ammonium sulfate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16794,T3D1476,Zinc formate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16795,T3D1477,Zinc propionate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16796,T3D1478,Zinc acetate dihydrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16797,T3D1479,Zinc fluoride hydrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16798,T3D1480,Zinc fluoride tetrahydrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16799,T3D1481,Zinc nitrate tetrahydrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16800,T3D1482,Zinc nitrate hexahydrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16801,T3D1483,Zinc sulfate monohydrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16802,T3D1484,Zinc sulfate hexahydrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16803,T3D1485,Zinc sulfate heptahydrate,Superoxide dismutase [Cu-Zn],P00441,"Unbalanced levels of copper and zinc binding to Cu,Zn-superoxide dismutase has been linked to amyotrophic lateral sclerosis (ALS). (R128)"
16804,T3D0703,Calcium chromate dihydrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16805,T3D0703,Calcium chromate dihydrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16806,T3D0703,Calcium chromate dihydrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16807,T3D0703,Calcium chromate dihydrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16808,T3D0703,Calcium chromate dihydrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16810,T3D1425,Potassium tetraperoxochromate(V),Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16811,T3D1425,Potassium tetraperoxochromate(V),Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16812,T3D1425,Potassium tetraperoxochromate(V),Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16813,T3D1425,Potassium tetraperoxochromate(V),Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16814,T3D1426,(Benzene)chromium tricarbonyl,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16815,T3D1426,(Benzene)chromium tricarbonyl,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16816,T3D1426,(Benzene)chromium tricarbonyl,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16817,T3D1426,(Benzene)chromium tricarbonyl,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16818,T3D1426,(Benzene)chromium tricarbonyl,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16819,T3D1427,Bis(benzene)chromium,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16820,T3D1427,Bis(benzene)chromium,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16821,T3D1427,Bis(benzene)chromium,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16822,T3D1427,Bis(benzene)chromium,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16823,T3D1427,Bis(benzene)chromium,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16824,T3D1428,Chromium(III) potassium sulfate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16825,T3D1428,Chromium(III) potassium sulfate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16826,T3D1428,Chromium(III) potassium sulfate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16827,T3D1428,Chromium(III) potassium sulfate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16828,T3D1428,Chromium(III) potassium sulfate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16829,T3D1429,Chromium(III) potassium sulfate dodecahydrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16830,T3D1429,Chromium(III) potassium sulfate dodecahydrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16831,T3D1429,Chromium(III) potassium sulfate dodecahydrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16832,T3D1429,Chromium(III) potassium sulfate dodecahydrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16833,T3D1429,Chromium(III) potassium sulfate dodecahydrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16834,T3D1430,Chromium carbide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16835,T3D1430,Chromium carbide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16836,T3D1430,Chromium carbide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16837,T3D1430,Chromium carbide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16838,T3D1430,Chromium carbide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16839,T3D1431,Chromium carbonyl,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16840,T3D1431,Chromium carbonyl,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16841,T3D1431,Chromium carbonyl,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16842,T3D1431,Chromium carbonyl,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16843,T3D1431,Chromium carbonyl,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16844,T3D1432,Chromium(III) nitrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16845,T3D1432,Chromium(III) nitrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16846,T3D1432,Chromium(III) nitrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16847,T3D1432,Chromium(III) nitrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16848,T3D1432,Chromium(III) nitrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16849,T3D1433,Chromium(III) nitrate nonahydrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16850,T3D1433,Chromium(III) nitrate nonahydrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16851,T3D1433,Chromium(III) nitrate nonahydrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16852,T3D1433,Chromium(III) nitrate nonahydrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16853,T3D1433,Chromium(III) nitrate nonahydrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16854,T3D1434,Chromium nitride,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16855,T3D1434,Chromium nitride,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16856,T3D1434,Chromium nitride,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16857,T3D1434,Chromium nitride,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16858,T3D1434,Chromium nitride,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16859,T3D1435,Chromium(II) acetate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16860,T3D1435,Chromium(II) acetate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16861,T3D1435,Chromium(II) acetate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16862,T3D1435,Chromium(II) acetate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16863,T3D1435,Chromium(II) acetate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16864,T3D1436,Chromium(II) chloride,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16865,T3D1436,Chromium(II) chloride,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16866,T3D1436,Chromium(II) chloride,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16867,T3D1436,Chromium(II) chloride,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16868,T3D1436,Chromium(II) chloride,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16869,T3D1437,Chromium(II) oxide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16870,T3D1437,Chromium(II) oxide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16871,T3D1437,Chromium(II) oxide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16872,T3D1437,Chromium(II) oxide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16873,T3D1437,Chromium(II) oxide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16874,T3D1438,Chromium(III) acetylacetonate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16875,T3D1438,Chromium(III) acetylacetonate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16876,T3D1438,Chromium(III) acetylacetonate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16877,T3D1438,Chromium(III) acetylacetonate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16878,T3D1438,Chromium(III) acetylacetonate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16879,T3D1439,Chromium(III) chloride,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16880,T3D1439,Chromium(III) chloride,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16881,T3D1439,Chromium(III) chloride,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16882,T3D1439,Chromium(III) chloride,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16883,T3D1439,Chromium(III) chloride,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16884,T3D1440,Chromium(III) chloride hexahydrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16885,T3D1440,Chromium(III) chloride hexahydrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16886,T3D1440,Chromium(III) chloride hexahydrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16887,T3D1440,Chromium(III) chloride hexahydrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16888,T3D1440,Chromium(III) chloride hexahydrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16889,T3D1441,Chromium(III) fluoride,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16890,T3D1441,Chromium(III) fluoride,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16891,T3D1441,Chromium(III) fluoride,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16892,T3D1441,Chromium(III) fluoride,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16893,T3D1441,Chromium(III) fluoride,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16894,T3D1442,Chromium(III) fluoride trihydrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16895,T3D1442,Chromium(III) fluoride trihydrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16896,T3D1442,Chromium(III) fluoride trihydrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16897,T3D1442,Chromium(III) fluoride trihydrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16898,T3D1442,Chromium(III) fluoride trihydrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16899,T3D1443,Chromium(III) fluoride tetrahydrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16900,T3D1443,Chromium(III) fluoride tetrahydrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16901,T3D1443,Chromium(III) fluoride tetrahydrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16902,T3D1443,Chromium(III) fluoride tetrahydrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16903,T3D1443,Chromium(III) fluoride tetrahydrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16904,T3D1444,Chromium(III) oxide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16905,T3D1444,Chromium(III) oxide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16906,T3D1444,Chromium(III) oxide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16907,T3D1444,Chromium(III) oxide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16908,T3D1444,Chromium(III) oxide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16909,T3D1445,Chromium(III) picolinate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16910,T3D1445,Chromium(III) picolinate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16911,T3D1445,Chromium(III) picolinate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16912,T3D1445,Chromium(III) picolinate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16913,T3D1445,Chromium(III) picolinate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16914,T3D1446,Chromium(III) sulfate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16915,T3D1446,Chromium(III) sulfate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16916,T3D1446,Chromium(III) sulfate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16917,T3D1446,Chromium(III) sulfate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16918,T3D1446,Chromium(III) sulfate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16919,T3D1447,Chromium(III) sulfate dodecahydrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16920,T3D1447,Chromium(III) sulfate dodecahydrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16921,T3D1447,Chromium(III) sulfate dodecahydrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16922,T3D1447,Chromium(III) sulfate dodecahydrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16923,T3D1447,Chromium(III) sulfate dodecahydrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16924,T3D1448,Chromium(III) sulfide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16925,T3D1448,Chromium(III) sulfide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16926,T3D1448,Chromium(III) sulfide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16927,T3D1448,Chromium(III) sulfide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16928,T3D1448,Chromium(III) sulfide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16929,T3D1449,Chromium(IV) oxide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16930,T3D1449,Chromium(IV) oxide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16931,T3D1449,Chromium(IV) oxide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16932,T3D1449,Chromium(IV) oxide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16933,T3D1449,Chromium(IV) oxide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16934,T3D1450,Chromocene,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16935,T3D1450,Chromocene,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16936,T3D1450,Chromocene,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16937,T3D1450,Chromocene,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16938,T3D1450,Chromocene,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16939,T3D1451,Chromyl chloride,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16940,T3D1451,Chromyl chloride,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16941,T3D1451,Chromyl chloride,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16942,T3D1451,Chromyl chloride,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16943,T3D1451,Chromyl chloride,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16944,T3D1452,Ammonium tetrathiocyanato-diamminechromate(III),DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16945,T3D1452,Ammonium tetrathiocyanato-diamminechromate(III),Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16946,T3D1452,Ammonium tetrathiocyanato-diamminechromate(III),Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16947,T3D1452,Ammonium tetrathiocyanato-diamminechromate(III),Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16948,T3D1452,Ammonium tetrathiocyanato-diamminechromate(III),Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16949,T3D1453,Sodium dichromate dihydrate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16950,T3D1453,Sodium dichromate dihydrate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16951,T3D1453,Sodium dichromate dihydrate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16952,T3D1453,Sodium dichromate dihydrate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16953,T3D1453,Sodium dichromate dihydrate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16954,T3D1454,Chromium trihydroxide,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16955,T3D1454,Chromium trihydroxide,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16956,T3D1454,Chromium trihydroxide,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16957,T3D1454,Chromium trihydroxide,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16958,T3D1454,Chromium trihydroxide,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16959,T3D1455,Chromium chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16960,T3D1455,Chromium chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16961,T3D1455,Chromium chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16962,T3D1455,Chromium chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16963,T3D1455,Chromium chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16964,T3D1456,Chromic chromate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16965,T3D1456,Chromic chromate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16966,T3D1456,Chromic chromate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16967,T3D1456,Chromic chromate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16968,T3D1456,Chromic chromate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16969,T3D1457,Chromium(II) oxalate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16970,T3D1457,Chromium(II) oxalate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16971,T3D1457,Chromium(II) oxalate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16972,T3D1457,Chromium(II) oxalate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16973,T3D1457,Chromium(II) oxalate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16974,T3D1458,Chromium(III) acetate,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16975,T3D1458,Chromium(III) acetate,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16976,T3D1458,Chromium(III) acetate,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16977,T3D1458,Chromium(III) acetate,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16978,T3D1458,Chromium(III) acetate,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16979,T3D1189,Copper chromite,DNA,DNA,"Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, chromium-DNA adducts, chromosomal aberrations and alterations in cellular signaling pathways. (R042)"
16980,T3D1189,Copper chromite,Histone deacetylase 1,Q13547,"Chromium can cause transcriptional repression by cross-linking histone deacetylase 1-DNA methyltransferase 1 complexes to CYP1A1 promoter chromatin, inhibiting histone modification. (R076)"
16981,T3D1189,Copper chromite,Metal regulatory transcription factor 1,Q14872,"Chromium may increase its own toxicity by modifying metal regulatory transcription factor 1, causing the inhibition of zinc-induced metallothionein transcription. (R077)"
16982,T3D1189,Copper chromite,Mitogen-activated protein kinase 1,P28482,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16983,T3D1189,Copper chromite,Mitogen-activated protein kinase 3,P27361,Chromium has been shown to induce carcinogenesis by overstimulating cellular regulatory pathways and increasing peroxide levels by activating certain mitogen-activated protein kinases. (R075)
16984,T3D1091,Aluminium barium titanium oxide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16985,T3D1091,Aluminium barium titanium oxide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16986,T3D1091,Aluminium barium titanium oxide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16987,T3D1091,Aluminium barium titanium oxide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16988,T3D1091,Aluminium barium titanium oxide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16989,T3D1091,Aluminium barium titanium oxide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16990,T3D1091,Aluminium barium titanium oxide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16991,T3D1091,Aluminium barium titanium oxide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
16992,T3D1091,Aluminium barium titanium oxide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16993,T3D1091,Aluminium barium titanium oxide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16994,T3D1091,Aluminium barium titanium oxide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16995,T3D1091,Aluminium barium titanium oxide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16996,T3D1091,Aluminium barium titanium oxide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16997,T3D1091,Aluminium barium titanium oxide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16998,T3D1091,Aluminium barium titanium oxide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
16999,T3D1091,Aluminium barium titanium oxide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17000,T3D1091,Aluminium barium titanium oxide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17001,T3D1091,Aluminium barium titanium oxide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17002,T3D1091,Aluminium barium titanium oxide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17003,T3D1091,Aluminium barium titanium oxide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17004,T3D1091,Aluminium barium titanium oxide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17005,T3D1092,Barium acetate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17006,T3D1092,Barium acetate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17007,T3D1092,Barium acetate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17008,T3D1092,Barium acetate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17009,T3D1092,Barium acetate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17010,T3D1092,Barium acetate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17011,T3D1092,Barium acetate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17012,T3D1092,Barium acetate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17013,T3D1092,Barium acetate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17014,T3D1092,Barium acetate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17015,T3D1092,Barium acetate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17016,T3D1092,Barium acetate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17017,T3D1092,Barium acetate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17018,T3D1092,Barium acetate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17019,T3D1092,Barium acetate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17020,T3D1092,Barium acetate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17021,T3D1092,Barium acetate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17022,T3D1092,Barium acetate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17023,T3D1092,Barium acetate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17024,T3D1092,Barium acetate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17025,T3D1092,Barium acetate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17026,T3D1093,Barium azide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17027,T3D1093,Barium azide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17028,T3D1093,Barium azide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17029,T3D1093,Barium azide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17030,T3D1093,Barium azide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17031,T3D1093,Barium azide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17032,T3D1093,Barium azide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17033,T3D1093,Barium azide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17034,T3D1093,Barium azide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17035,T3D1093,Barium azide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17036,T3D1093,Barium azide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17037,T3D1093,Barium azide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17038,T3D1093,Barium azide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17039,T3D1093,Barium azide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17040,T3D1093,Barium azide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17041,T3D1093,Barium azide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17042,T3D1093,Barium azide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17043,T3D1093,Barium azide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17044,T3D1093,Barium azide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17045,T3D1093,Barium azide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17046,T3D1093,Barium azide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17047,T3D1094,Barium bromate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17048,T3D1094,Barium bromate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17049,T3D1094,Barium bromate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17050,T3D1094,Barium bromate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17051,T3D1094,Barium bromate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17052,T3D1094,Barium bromate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17053,T3D1094,Barium bromate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17054,T3D1094,Barium bromate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17055,T3D1094,Barium bromate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17056,T3D1094,Barium bromate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17057,T3D1094,Barium bromate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17058,T3D1094,Barium bromate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17059,T3D1094,Barium bromate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17060,T3D1094,Barium bromate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17061,T3D1094,Barium bromate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17062,T3D1094,Barium bromate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17063,T3D1094,Barium bromate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17064,T3D1094,Barium bromate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17065,T3D1094,Barium bromate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17066,T3D1094,Barium bromate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17067,T3D1094,Barium bromate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17068,T3D1095,Barium bromide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17069,T3D1095,Barium bromide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17070,T3D1095,Barium bromide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17071,T3D1095,Barium bromide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17072,T3D1095,Barium bromide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17073,T3D1095,Barium bromide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17074,T3D1095,Barium bromide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17075,T3D1095,Barium bromide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17076,T3D1095,Barium bromide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17077,T3D1095,Barium bromide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17078,T3D1095,Barium bromide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17079,T3D1095,Barium bromide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17080,T3D1095,Barium bromide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17081,T3D1095,Barium bromide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17082,T3D1095,Barium bromide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17083,T3D1095,Barium bromide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17084,T3D1095,Barium bromide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17085,T3D1095,Barium bromide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17086,T3D1095,Barium bromide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17087,T3D1095,Barium bromide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17088,T3D1095,Barium bromide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17089,T3D1096,Barium bromide dihydrate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17090,T3D1096,Barium bromide dihydrate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17091,T3D1096,Barium bromide dihydrate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17092,T3D1096,Barium bromide dihydrate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17093,T3D1096,Barium bromide dihydrate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17094,T3D1096,Barium bromide dihydrate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17095,T3D1096,Barium bromide dihydrate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17096,T3D1096,Barium bromide dihydrate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17097,T3D1096,Barium bromide dihydrate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17098,T3D1096,Barium bromide dihydrate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17099,T3D1096,Barium bromide dihydrate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17100,T3D1096,Barium bromide dihydrate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17101,T3D1096,Barium bromide dihydrate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17102,T3D1096,Barium bromide dihydrate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17103,T3D1096,Barium bromide dihydrate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17104,T3D1096,Barium bromide dihydrate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17105,T3D1096,Barium bromide dihydrate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17106,T3D1096,Barium bromide dihydrate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17107,T3D1096,Barium bromide dihydrate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17108,T3D1096,Barium bromide dihydrate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17109,T3D1096,Barium bromide dihydrate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17110,T3D1097,Barium cadmium stearate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17111,T3D1097,Barium cadmium stearate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17112,T3D1097,Barium cadmium stearate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17113,T3D1097,Barium cadmium stearate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17114,T3D1097,Barium cadmium stearate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17115,T3D1097,Barium cadmium stearate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17116,T3D1097,Barium cadmium stearate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17117,T3D1097,Barium cadmium stearate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17118,T3D1097,Barium cadmium stearate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17119,T3D1097,Barium cadmium stearate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17120,T3D1097,Barium cadmium stearate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17121,T3D1097,Barium cadmium stearate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17122,T3D1097,Barium cadmium stearate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17123,T3D1097,Barium cadmium stearate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17124,T3D1097,Barium cadmium stearate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17125,T3D1097,Barium cadmium stearate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17126,T3D1097,Barium cadmium stearate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17127,T3D1097,Barium cadmium stearate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17128,T3D1097,Barium cadmium stearate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17129,T3D1097,Barium cadmium stearate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17130,T3D1097,Barium cadmium stearate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17131,T3D1098,Barium calcium titanium oxide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17132,T3D1098,Barium calcium titanium oxide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17133,T3D1098,Barium calcium titanium oxide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17134,T3D1098,Barium calcium titanium oxide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17135,T3D1098,Barium calcium titanium oxide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17136,T3D1098,Barium calcium titanium oxide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17137,T3D1098,Barium calcium titanium oxide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17138,T3D1098,Barium calcium titanium oxide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17139,T3D1098,Barium calcium titanium oxide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17140,T3D1098,Barium calcium titanium oxide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17141,T3D1098,Barium calcium titanium oxide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17142,T3D1098,Barium calcium titanium oxide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17143,T3D1098,Barium calcium titanium oxide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17144,T3D1098,Barium calcium titanium oxide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17145,T3D1098,Barium calcium titanium oxide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17146,T3D1098,Barium calcium titanium oxide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17147,T3D1098,Barium calcium titanium oxide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17148,T3D1098,Barium calcium titanium oxide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17149,T3D1098,Barium calcium titanium oxide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17150,T3D1098,Barium calcium titanium oxide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17151,T3D1098,Barium calcium titanium oxide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17152,T3D1099,Barium carbonate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17153,T3D1099,Barium carbonate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17154,T3D1099,Barium carbonate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17155,T3D1099,Barium carbonate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17156,T3D1099,Barium carbonate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17157,T3D1099,Barium carbonate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17158,T3D1099,Barium carbonate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17159,T3D1099,Barium carbonate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17160,T3D1099,Barium carbonate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17161,T3D1099,Barium carbonate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17162,T3D1099,Barium carbonate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17163,T3D1099,Barium carbonate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17164,T3D1099,Barium carbonate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17165,T3D1099,Barium carbonate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17166,T3D1099,Barium carbonate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17167,T3D1099,Barium carbonate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17168,T3D1099,Barium carbonate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17169,T3D1099,Barium carbonate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17170,T3D1099,Barium carbonate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17171,T3D1099,Barium carbonate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17172,T3D1099,Barium carbonate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17173,T3D1100,Barium chlorate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17174,T3D1100,Barium chlorate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17175,T3D1100,Barium chlorate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17176,T3D1100,Barium chlorate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17177,T3D1100,Barium chlorate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17178,T3D1100,Barium chlorate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17179,T3D1100,Barium chlorate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17180,T3D1100,Barium chlorate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17181,T3D1100,Barium chlorate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17182,T3D1100,Barium chlorate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17183,T3D1100,Barium chlorate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17184,T3D1100,Barium chlorate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17185,T3D1100,Barium chlorate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17186,T3D1100,Barium chlorate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17187,T3D1100,Barium chlorate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17188,T3D1100,Barium chlorate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17189,T3D1100,Barium chlorate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17190,T3D1100,Barium chlorate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17191,T3D1100,Barium chlorate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17192,T3D1100,Barium chlorate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17193,T3D1100,Barium chlorate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17194,T3D1101,Barium chloride,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17195,T3D1101,Barium chloride,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17196,T3D1101,Barium chloride,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17197,T3D1101,Barium chloride,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17198,T3D1101,Barium chloride,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17199,T3D1101,Barium chloride,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17200,T3D1101,Barium chloride,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17201,T3D1101,Barium chloride,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17202,T3D1101,Barium chloride,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17203,T3D1101,Barium chloride,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17204,T3D1101,Barium chloride,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17205,T3D1101,Barium chloride,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17206,T3D1101,Barium chloride,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17207,T3D1101,Barium chloride,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17208,T3D1101,Barium chloride,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17209,T3D1101,Barium chloride,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17210,T3D1101,Barium chloride,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17211,T3D1101,Barium chloride,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17212,T3D1101,Barium chloride,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17213,T3D1101,Barium chloride,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17214,T3D1101,Barium chloride,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17215,T3D1102,Barium chloride dihydrate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17216,T3D1102,Barium chloride dihydrate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17217,T3D1102,Barium chloride dihydrate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17218,T3D1102,Barium chloride dihydrate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17219,T3D1102,Barium chloride dihydrate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17220,T3D1102,Barium chloride dihydrate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17221,T3D1102,Barium chloride dihydrate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17222,T3D1102,Barium chloride dihydrate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17223,T3D1102,Barium chloride dihydrate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17224,T3D1102,Barium chloride dihydrate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17225,T3D1102,Barium chloride dihydrate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17226,T3D1102,Barium chloride dihydrate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17227,T3D1102,Barium chloride dihydrate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17228,T3D1102,Barium chloride dihydrate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17229,T3D1102,Barium chloride dihydrate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17230,T3D1102,Barium chloride dihydrate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17231,T3D1102,Barium chloride dihydrate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17232,T3D1102,Barium chloride dihydrate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17233,T3D1102,Barium chloride dihydrate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17234,T3D1102,Barium chloride dihydrate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17235,T3D1102,Barium chloride dihydrate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17236,T3D1103,Barium cyanide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17237,T3D1103,Barium cyanide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17238,T3D1103,Barium cyanide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17239,T3D1103,Barium cyanide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17240,T3D1103,Barium cyanide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17241,T3D1103,Barium cyanide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17242,T3D1103,Barium cyanide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17243,T3D1103,Barium cyanide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17244,T3D1103,Barium cyanide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17245,T3D1103,Barium cyanide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17246,T3D1103,Barium cyanide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17247,T3D1103,Barium cyanide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17248,T3D1103,Barium cyanide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17249,T3D1103,Barium cyanide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17250,T3D1103,Barium cyanide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17251,T3D1103,Barium cyanide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17252,T3D1103,Barium cyanide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17253,T3D1103,Barium cyanide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17254,T3D1103,Barium cyanide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17255,T3D1103,Barium cyanide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17256,T3D1103,Barium cyanide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17257,T3D1104,Barium ferrate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17258,T3D1104,Barium ferrate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17259,T3D1104,Barium ferrate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17260,T3D1104,Barium ferrate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17261,T3D1104,Barium ferrate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17262,T3D1104,Barium ferrate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17263,T3D1104,Barium ferrate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17264,T3D1104,Barium ferrate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17265,T3D1104,Barium ferrate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17266,T3D1104,Barium ferrate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17267,T3D1104,Barium ferrate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17268,T3D1104,Barium ferrate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17269,T3D1104,Barium ferrate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17270,T3D1104,Barium ferrate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17271,T3D1104,Barium ferrate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17272,T3D1104,Barium ferrate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17273,T3D1104,Barium ferrate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17274,T3D1104,Barium ferrate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17275,T3D1104,Barium ferrate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17276,T3D1104,Barium ferrate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17277,T3D1104,Barium ferrate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17278,T3D1105,Barium ferrite,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17279,T3D1105,Barium ferrite,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17280,T3D1105,Barium ferrite,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17281,T3D1105,Barium ferrite,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17282,T3D1105,Barium ferrite,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17283,T3D1105,Barium ferrite,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17284,T3D1105,Barium ferrite,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17285,T3D1105,Barium ferrite,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17286,T3D1105,Barium ferrite,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17287,T3D1105,Barium ferrite,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17288,T3D1105,Barium ferrite,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17289,T3D1105,Barium ferrite,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17290,T3D1105,Barium ferrite,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17291,T3D1105,Barium ferrite,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17292,T3D1105,Barium ferrite,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17293,T3D1105,Barium ferrite,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17294,T3D1105,Barium ferrite,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17295,T3D1105,Barium ferrite,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17296,T3D1105,Barium ferrite,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17297,T3D1105,Barium ferrite,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17298,T3D1105,Barium ferrite,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17299,T3D1106,Barium fluoborate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17300,T3D1106,Barium fluoborate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17301,T3D1106,Barium fluoborate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17302,T3D1106,Barium fluoborate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17303,T3D1106,Barium fluoborate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17304,T3D1106,Barium fluoborate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17305,T3D1106,Barium fluoborate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17306,T3D1106,Barium fluoborate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17307,T3D1106,Barium fluoborate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17308,T3D1106,Barium fluoborate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17309,T3D1106,Barium fluoborate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17310,T3D1106,Barium fluoborate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17311,T3D1106,Barium fluoborate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17312,T3D1106,Barium fluoborate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17313,T3D1106,Barium fluoborate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17314,T3D1106,Barium fluoborate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17315,T3D1106,Barium fluoborate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17316,T3D1106,Barium fluoborate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17317,T3D1106,Barium fluoborate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17318,T3D1106,Barium fluoborate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17319,T3D1106,Barium fluoborate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17320,T3D1107,Barium fluoride,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17321,T3D1107,Barium fluoride,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17322,T3D1107,Barium fluoride,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17323,T3D1107,Barium fluoride,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17324,T3D1107,Barium fluoride,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17325,T3D1107,Barium fluoride,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17326,T3D1107,Barium fluoride,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17327,T3D1107,Barium fluoride,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17328,T3D1107,Barium fluoride,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17329,T3D1107,Barium fluoride,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17330,T3D1107,Barium fluoride,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17331,T3D1107,Barium fluoride,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17332,T3D1107,Barium fluoride,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17333,T3D1107,Barium fluoride,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17334,T3D1107,Barium fluoride,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17335,T3D1107,Barium fluoride,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17336,T3D1107,Barium fluoride,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17337,T3D1107,Barium fluoride,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17338,T3D1107,Barium fluoride,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17339,T3D1107,Barium fluoride,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17340,T3D1107,Barium fluoride,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17341,T3D1108,Barium hydroxide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17342,T3D1108,Barium hydroxide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17343,T3D1108,Barium hydroxide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17344,T3D1108,Barium hydroxide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17345,T3D1108,Barium hydroxide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17346,T3D1108,Barium hydroxide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17347,T3D1108,Barium hydroxide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17348,T3D1108,Barium hydroxide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17349,T3D1108,Barium hydroxide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17350,T3D1108,Barium hydroxide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17351,T3D1108,Barium hydroxide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17352,T3D1108,Barium hydroxide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17353,T3D1108,Barium hydroxide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17354,T3D1108,Barium hydroxide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17355,T3D1108,Barium hydroxide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17356,T3D1108,Barium hydroxide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17357,T3D1108,Barium hydroxide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17358,T3D1108,Barium hydroxide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17359,T3D1108,Barium hydroxide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17360,T3D1108,Barium hydroxide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17361,T3D1108,Barium hydroxide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17362,T3D1109,Barium hydroxide monohydrate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17363,T3D1109,Barium hydroxide monohydrate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17364,T3D1109,Barium hydroxide monohydrate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17365,T3D1109,Barium hydroxide monohydrate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17366,T3D1109,Barium hydroxide monohydrate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17367,T3D1109,Barium hydroxide monohydrate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17368,T3D1109,Barium hydroxide monohydrate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17369,T3D1109,Barium hydroxide monohydrate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17370,T3D1109,Barium hydroxide monohydrate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17371,T3D1109,Barium hydroxide monohydrate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17372,T3D1109,Barium hydroxide monohydrate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17373,T3D1109,Barium hydroxide monohydrate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17374,T3D1109,Barium hydroxide monohydrate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17375,T3D1109,Barium hydroxide monohydrate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17376,T3D1109,Barium hydroxide monohydrate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17377,T3D1109,Barium hydroxide monohydrate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17378,T3D1109,Barium hydroxide monohydrate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17379,T3D1109,Barium hydroxide monohydrate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17380,T3D1109,Barium hydroxide monohydrate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17381,T3D1109,Barium hydroxide monohydrate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17382,T3D1109,Barium hydroxide monohydrate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17383,T3D1110,Barium hydroxide octahydrate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17384,T3D1110,Barium hydroxide octahydrate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17385,T3D1110,Barium hydroxide octahydrate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17386,T3D1110,Barium hydroxide octahydrate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17387,T3D1110,Barium hydroxide octahydrate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17388,T3D1110,Barium hydroxide octahydrate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17389,T3D1110,Barium hydroxide octahydrate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17390,T3D1110,Barium hydroxide octahydrate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17391,T3D1110,Barium hydroxide octahydrate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17392,T3D1110,Barium hydroxide octahydrate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17393,T3D1110,Barium hydroxide octahydrate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17394,T3D1110,Barium hydroxide octahydrate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17395,T3D1110,Barium hydroxide octahydrate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17396,T3D1110,Barium hydroxide octahydrate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17397,T3D1110,Barium hydroxide octahydrate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17398,T3D1110,Barium hydroxide octahydrate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17399,T3D1110,Barium hydroxide octahydrate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17400,T3D1110,Barium hydroxide octahydrate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17401,T3D1110,Barium hydroxide octahydrate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17402,T3D1110,Barium hydroxide octahydrate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17403,T3D1110,Barium hydroxide octahydrate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17404,T3D1111,Barium hypochlorite,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17405,T3D1111,Barium hypochlorite,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17406,T3D1111,Barium hypochlorite,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17407,T3D1111,Barium hypochlorite,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17408,T3D1111,Barium hypochlorite,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17409,T3D1111,Barium hypochlorite,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17410,T3D1111,Barium hypochlorite,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17411,T3D1111,Barium hypochlorite,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17412,T3D1111,Barium hypochlorite,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17413,T3D1111,Barium hypochlorite,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17414,T3D1111,Barium hypochlorite,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17415,T3D1111,Barium hypochlorite,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17416,T3D1111,Barium hypochlorite,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17417,T3D1111,Barium hypochlorite,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17418,T3D1111,Barium hypochlorite,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17419,T3D1111,Barium hypochlorite,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17420,T3D1111,Barium hypochlorite,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17421,T3D1111,Barium hypochlorite,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17422,T3D1111,Barium hypochlorite,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17423,T3D1111,Barium hypochlorite,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17424,T3D1111,Barium hypochlorite,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17425,T3D1112,Barium iodide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17426,T3D1112,Barium iodide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17427,T3D1112,Barium iodide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17428,T3D1112,Barium iodide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17429,T3D1112,Barium iodide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17430,T3D1112,Barium iodide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17431,T3D1112,Barium iodide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17432,T3D1112,Barium iodide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17433,T3D1112,Barium iodide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17434,T3D1112,Barium iodide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17435,T3D1112,Barium iodide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17436,T3D1112,Barium iodide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17437,T3D1112,Barium iodide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17438,T3D1112,Barium iodide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17439,T3D1112,Barium iodide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17440,T3D1112,Barium iodide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17441,T3D1112,Barium iodide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17442,T3D1112,Barium iodide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17443,T3D1112,Barium iodide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17444,T3D1112,Barium iodide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17445,T3D1112,Barium iodide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17446,T3D1113,Barium iodide dihydrate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17447,T3D1113,Barium iodide dihydrate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17448,T3D1113,Barium iodide dihydrate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17449,T3D1113,Barium iodide dihydrate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17450,T3D1113,Barium iodide dihydrate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17451,T3D1113,Barium iodide dihydrate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17452,T3D1113,Barium iodide dihydrate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17453,T3D1113,Barium iodide dihydrate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17454,T3D1113,Barium iodide dihydrate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17455,T3D1113,Barium iodide dihydrate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17456,T3D1113,Barium iodide dihydrate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17457,T3D1113,Barium iodide dihydrate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17458,T3D1113,Barium iodide dihydrate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17459,T3D1113,Barium iodide dihydrate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17460,T3D1113,Barium iodide dihydrate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17461,T3D1113,Barium iodide dihydrate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17462,T3D1113,Barium iodide dihydrate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17463,T3D1113,Barium iodide dihydrate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17464,T3D1113,Barium iodide dihydrate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17465,T3D1113,Barium iodide dihydrate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17466,T3D1113,Barium iodide dihydrate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17467,T3D1114,Barium iron oxide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17468,T3D1114,Barium iron oxide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17469,T3D1114,Barium iron oxide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17470,T3D1114,Barium iron oxide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17471,T3D1114,Barium iron oxide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17472,T3D1114,Barium iron oxide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17473,T3D1114,Barium iron oxide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17474,T3D1114,Barium iron oxide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17475,T3D1114,Barium iron oxide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17476,T3D1114,Barium iron oxide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17477,T3D1114,Barium iron oxide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17478,T3D1114,Barium iron oxide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17479,T3D1114,Barium iron oxide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17480,T3D1114,Barium iron oxide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17481,T3D1114,Barium iron oxide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17482,T3D1114,Barium iron oxide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17483,T3D1114,Barium iron oxide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17484,T3D1114,Barium iron oxide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17485,T3D1114,Barium iron oxide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17486,T3D1114,Barium iron oxide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17487,T3D1114,Barium iron oxide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17488,T3D1115,Barium nitrate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17489,T3D1115,Barium nitrate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17490,T3D1115,Barium nitrate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17491,T3D1115,Barium nitrate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17492,T3D1115,Barium nitrate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17493,T3D1115,Barium nitrate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17494,T3D1115,Barium nitrate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17495,T3D1115,Barium nitrate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17496,T3D1115,Barium nitrate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17497,T3D1115,Barium nitrate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17498,T3D1115,Barium nitrate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17499,T3D1115,Barium nitrate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17500,T3D1115,Barium nitrate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17501,T3D1115,Barium nitrate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17502,T3D1115,Barium nitrate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17503,T3D1115,Barium nitrate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17504,T3D1115,Barium nitrate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17505,T3D1115,Barium nitrate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17506,T3D1115,Barium nitrate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17507,T3D1115,Barium nitrate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17508,T3D1115,Barium nitrate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17509,T3D1116,Barium oxalate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17510,T3D1116,Barium oxalate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17511,T3D1116,Barium oxalate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17512,T3D1116,Barium oxalate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17513,T3D1116,Barium oxalate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17514,T3D1116,Barium oxalate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17515,T3D1116,Barium oxalate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17516,T3D1116,Barium oxalate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17517,T3D1116,Barium oxalate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17518,T3D1116,Barium oxalate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17519,T3D1116,Barium oxalate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17520,T3D1116,Barium oxalate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17521,T3D1116,Barium oxalate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17522,T3D1116,Barium oxalate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17523,T3D1116,Barium oxalate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17524,T3D1116,Barium oxalate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17525,T3D1116,Barium oxalate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17526,T3D1116,Barium oxalate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17527,T3D1116,Barium oxalate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17528,T3D1116,Barium oxalate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17529,T3D1116,Barium oxalate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17530,T3D1117,Barium oxide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17531,T3D1117,Barium oxide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17532,T3D1117,Barium oxide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17533,T3D1117,Barium oxide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17534,T3D1117,Barium oxide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17535,T3D1117,Barium oxide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17536,T3D1117,Barium oxide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17537,T3D1117,Barium oxide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17538,T3D1117,Barium oxide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17539,T3D1117,Barium oxide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17540,T3D1117,Barium oxide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17541,T3D1117,Barium oxide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17542,T3D1117,Barium oxide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17543,T3D1117,Barium oxide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17544,T3D1117,Barium oxide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17545,T3D1117,Barium oxide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17546,T3D1117,Barium oxide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17547,T3D1117,Barium oxide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17548,T3D1117,Barium oxide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17549,T3D1117,Barium oxide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17550,T3D1117,Barium oxide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17551,T3D1118,Barium perchlorate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17552,T3D1118,Barium perchlorate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17553,T3D1118,Barium perchlorate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17554,T3D1118,Barium perchlorate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17555,T3D1118,Barium perchlorate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17556,T3D1118,Barium perchlorate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17557,T3D1118,Barium perchlorate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17558,T3D1118,Barium perchlorate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17559,T3D1118,Barium perchlorate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17560,T3D1118,Barium perchlorate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17561,T3D1118,Barium perchlorate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17562,T3D1118,Barium perchlorate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17563,T3D1118,Barium perchlorate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17564,T3D1118,Barium perchlorate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17565,T3D1118,Barium perchlorate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17566,T3D1118,Barium perchlorate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17567,T3D1118,Barium perchlorate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17568,T3D1118,Barium perchlorate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17569,T3D1118,Barium perchlorate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17570,T3D1118,Barium perchlorate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17571,T3D1118,Barium perchlorate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17572,T3D1119,Barium permanganate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17573,T3D1119,Barium permanganate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17574,T3D1119,Barium permanganate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17575,T3D1119,Barium permanganate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17576,T3D1119,Barium permanganate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17577,T3D1119,Barium permanganate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17578,T3D1119,Barium permanganate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17579,T3D1119,Barium permanganate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17580,T3D1119,Barium permanganate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17581,T3D1119,Barium permanganate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17582,T3D1119,Barium permanganate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17583,T3D1119,Barium permanganate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17584,T3D1119,Barium permanganate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17585,T3D1119,Barium permanganate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17586,T3D1119,Barium permanganate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17587,T3D1119,Barium permanganate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17588,T3D1119,Barium permanganate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17589,T3D1119,Barium permanganate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17590,T3D1119,Barium permanganate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17591,T3D1119,Barium permanganate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17592,T3D1119,Barium permanganate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17593,T3D1120,Barium peroxide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17594,T3D1120,Barium peroxide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17595,T3D1120,Barium peroxide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17596,T3D1120,Barium peroxide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17597,T3D1120,Barium peroxide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17598,T3D1120,Barium peroxide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17599,T3D1120,Barium peroxide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17600,T3D1120,Barium peroxide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17601,T3D1120,Barium peroxide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17602,T3D1120,Barium peroxide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17603,T3D1120,Barium peroxide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17604,T3D1120,Barium peroxide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17605,T3D1120,Barium peroxide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17606,T3D1120,Barium peroxide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17607,T3D1120,Barium peroxide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17608,T3D1120,Barium peroxide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17609,T3D1120,Barium peroxide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17610,T3D1120,Barium peroxide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17611,T3D1120,Barium peroxide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17612,T3D1120,Barium peroxide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17613,T3D1120,Barium peroxide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17614,T3D1121,Barium silicofluoride,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17615,T3D1121,Barium silicofluoride,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17616,T3D1121,Barium silicofluoride,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17617,T3D1121,Barium silicofluoride,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17618,T3D1121,Barium silicofluoride,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17619,T3D1121,Barium silicofluoride,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17620,T3D1121,Barium silicofluoride,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17621,T3D1121,Barium silicofluoride,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17622,T3D1121,Barium silicofluoride,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17623,T3D1121,Barium silicofluoride,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17624,T3D1121,Barium silicofluoride,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17625,T3D1121,Barium silicofluoride,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17626,T3D1121,Barium silicofluoride,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17627,T3D1121,Barium silicofluoride,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17628,T3D1121,Barium silicofluoride,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17629,T3D1121,Barium silicofluoride,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17630,T3D1121,Barium silicofluoride,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17631,T3D1121,Barium silicofluoride,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17632,T3D1121,Barium silicofluoride,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17633,T3D1121,Barium silicofluoride,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17634,T3D1121,Barium silicofluoride,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17635,T3D1122,Barium sulfate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17636,T3D1122,Barium sulfate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17637,T3D1122,Barium sulfate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17638,T3D1122,Barium sulfate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17639,T3D1122,Barium sulfate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17640,T3D1122,Barium sulfate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17641,T3D1122,Barium sulfate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17642,T3D1122,Barium sulfate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17643,T3D1122,Barium sulfate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17644,T3D1122,Barium sulfate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17645,T3D1122,Barium sulfate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17646,T3D1122,Barium sulfate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17647,T3D1122,Barium sulfate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17648,T3D1122,Barium sulfate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17649,T3D1122,Barium sulfate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17650,T3D1122,Barium sulfate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17651,T3D1122,Barium sulfate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17652,T3D1122,Barium sulfate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17653,T3D1122,Barium sulfate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17654,T3D1122,Barium sulfate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17655,T3D1122,Barium sulfate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17656,T3D1123,Barium sulfide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17657,T3D1123,Barium sulfide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17658,T3D1123,Barium sulfide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17659,T3D1123,Barium sulfide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17660,T3D1123,Barium sulfide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17661,T3D1123,Barium sulfide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17662,T3D1123,Barium sulfide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17663,T3D1123,Barium sulfide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17664,T3D1123,Barium sulfide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17665,T3D1123,Barium sulfide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17666,T3D1123,Barium sulfide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17667,T3D1123,Barium sulfide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17668,T3D1123,Barium sulfide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17669,T3D1123,Barium sulfide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17670,T3D1123,Barium sulfide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17671,T3D1123,Barium sulfide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17672,T3D1123,Barium sulfide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17673,T3D1123,Barium sulfide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17674,T3D1123,Barium sulfide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17675,T3D1123,Barium sulfide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17676,T3D1123,Barium sulfide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17677,T3D1124,Barium titanate,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17678,T3D1124,Barium titanate,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17679,T3D1124,Barium titanate,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17680,T3D1124,Barium titanate,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17681,T3D1124,Barium titanate,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17682,T3D1124,Barium titanate,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17683,T3D1124,Barium titanate,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17684,T3D1124,Barium titanate,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17685,T3D1124,Barium titanate,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17686,T3D1124,Barium titanate,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17687,T3D1124,Barium titanate,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17688,T3D1124,Barium titanate,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17689,T3D1124,Barium titanate,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17690,T3D1124,Barium titanate,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17691,T3D1124,Barium titanate,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17692,T3D1124,Barium titanate,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17693,T3D1124,Barium titanate,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17694,T3D1124,Barium titanate,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17695,T3D1124,Barium titanate,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17696,T3D1124,Barium titanate,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17697,T3D1124,Barium titanate,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17719,T3D1126,Barium zirconium oxide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17720,T3D1126,Barium zirconium oxide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17721,T3D1126,Barium zirconium oxide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17722,T3D1126,Barium zirconium oxide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17723,T3D1126,Barium zirconium oxide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17724,T3D1126,Barium zirconium oxide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17725,T3D1126,Barium zirconium oxide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17726,T3D1126,Barium zirconium oxide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17727,T3D1126,Barium zirconium oxide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17728,T3D1126,Barium zirconium oxide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17729,T3D1126,Barium zirconium oxide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17730,T3D1126,Barium zirconium oxide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17731,T3D1126,Barium zirconium oxide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17732,T3D1126,Barium zirconium oxide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17733,T3D1126,Barium zirconium oxide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17734,T3D1126,Barium zirconium oxide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17735,T3D1126,Barium zirconium oxide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17736,T3D1126,Barium zirconium oxide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17737,T3D1126,Barium zirconium oxide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17738,T3D1126,Barium zirconium oxide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17739,T3D1126,Barium zirconium oxide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17740,T3D1127,Yttrium barium copper oxide,ATP-sensitive inward rectifier potassium channel 1,P48048,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17741,T3D1127,Yttrium barium copper oxide,ATP-sensitive inward rectifier potassium channel 10,P78508,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17742,T3D1127,Yttrium barium copper oxide,ATP-sensitive inward rectifier potassium channel 11,Q14654,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17743,T3D1127,Yttrium barium copper oxide,ATP-sensitive inward rectifier potassium channel 12,Q14500,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17744,T3D1127,Yttrium barium copper oxide,ATP-sensitive inward rectifier potassium channel 14,Q9UNX9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17745,T3D1127,Yttrium barium copper oxide,ATP-sensitive inward rectifier potassium channel 15,Q99712,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17746,T3D1127,Yttrium barium copper oxide,ATP-sensitive inward rectifier potassium channel 8,Q15842,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17747,T3D1127,Yttrium barium copper oxide,Calmodulin,P62158,"Barium is believed to bind and activate calmodulin, causing certain neurotoxic effects. (R413)"
17748,T3D1127,Yttrium barium copper oxide,G protein-activated inward rectifier potassium channel 1,P48549,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17749,T3D1127,Yttrium barium copper oxide,G protein-activated inward rectifier potassium channel 2,P48051,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17750,T3D1127,Yttrium barium copper oxide,G protein-activated inward rectifier potassium channel 3,Q92806,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17751,T3D1127,Yttrium barium copper oxide,G protein-activated inward rectifier potassium channel 4,P48544,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17752,T3D1127,Yttrium barium copper oxide,Inward rectifier potassium channel 13,O60928,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17753,T3D1127,Yttrium barium copper oxide,Inward rectifier potassium channel 16,Q9NPI9,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17754,T3D1127,Yttrium barium copper oxide,Inward rectifier potassium channel 2,P63252,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17755,T3D1127,Yttrium barium copper oxide,Inward rectifier potassium channel 4,P48050,"Barium is a competitive antagonist at inward rectifier potassium channels and blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R418)"
17756,T3D1127,Yttrium barium copper oxide,Potassium voltage-gated channel subfamily KQT member 1,P51787,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17757,T3D1127,Yttrium barium copper oxide,Potassium voltage-gated channel subfamily KQT member 2,O43526,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17758,T3D1127,Yttrium barium copper oxide,Potassium voltage-gated channel subfamily KQT member 3,O43525,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17759,T3D1127,Yttrium barium copper oxide,Potassium voltage-gated channel subfamily KQT member 4,P56696,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17760,T3D1127,Yttrium barium copper oxide,Potassium voltage-gated channel subfamily KQT member 5,Q9NR82,"Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to intracellular compartments. The intracellular translocation of potassium results in a decreased resting membrane potential, making the muscle fibers electrically unexcitable and causing paralysis. (R419)"
17761,T3D1128,Manganese chloride,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17762,T3D1128,Manganese chloride,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17763,T3D1128,Manganese chloride,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17764,T3D1128,Manganese chloride,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17765,T3D1128,Manganese chloride,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17766,T3D1129,Manganese chloride dihydrate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17767,T3D1129,Manganese chloride dihydrate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17768,T3D1129,Manganese chloride dihydrate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17769,T3D1129,Manganese chloride dihydrate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17770,T3D1129,Manganese chloride dihydrate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17771,T3D1130,Manganese chloride tetrahydrate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17772,T3D1130,Manganese chloride tetrahydrate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17773,T3D1130,Manganese chloride tetrahydrate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17774,T3D1130,Manganese chloride tetrahydrate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17775,T3D1130,Manganese chloride tetrahydrate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17776,T3D1131,Manganese sulfate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17777,T3D1131,Manganese sulfate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17778,T3D1131,Manganese sulfate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17779,T3D1131,Manganese sulfate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17780,T3D1131,Manganese sulfate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17781,T3D1132,Manganese sulfate monohydrate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17782,T3D1132,Manganese sulfate monohydrate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17783,T3D1132,Manganese sulfate monohydrate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17784,T3D1132,Manganese sulfate monohydrate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17785,T3D1132,Manganese sulfate monohydrate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17786,T3D1133,Manganese sulfate tetrahydrate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17787,T3D1133,Manganese sulfate tetrahydrate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17788,T3D1133,Manganese sulfate tetrahydrate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17789,T3D1133,Manganese sulfate tetrahydrate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17790,T3D1133,Manganese sulfate tetrahydrate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17791,T3D1134,"Manganese(II,III) oxide","Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17792,T3D1134,"Manganese(II,III) oxide",Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17793,T3D1134,"Manganese(II,III) oxide",Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17794,T3D1134,"Manganese(II,III) oxide",Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17795,T3D1134,"Manganese(II,III) oxide",Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17796,T3D1135,Manganese dioxide,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17797,T3D1135,Manganese dioxide,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17798,T3D1135,Manganese dioxide,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17799,T3D1135,Manganese dioxide,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17800,T3D1135,Manganese dioxide,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17801,T3D1136,Potassium permanganate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17802,T3D1136,Potassium permanganate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17803,T3D1136,Potassium permanganate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17804,T3D1136,Potassium permanganate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17805,T3D1136,Potassium permanganate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17806,T3D1137,Mangafodipir,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17807,T3D1137,Mangafodipir,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17808,T3D1137,Mangafodipir,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17809,T3D1137,Mangafodipir,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17810,T3D1137,Mangafodipir,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17811,T3D1138,Methylcyclopentadienyl manganese tricarbonyl,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17812,T3D1138,Methylcyclopentadienyl manganese tricarbonyl,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17813,T3D1138,Methylcyclopentadienyl manganese tricarbonyl,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17814,T3D1138,Methylcyclopentadienyl manganese tricarbonyl,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17815,T3D1138,Methylcyclopentadienyl manganese tricarbonyl,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17816,T3D1139,Manganese(II) oxide,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17817,T3D1139,Manganese(II) oxide,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17818,T3D1139,Manganese(II) oxide,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17819,T3D1139,Manganese(II) oxide,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17820,T3D1139,Manganese(II) oxide,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17821,T3D1140,Dimanganese decacarbonyl,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17822,T3D1140,Dimanganese decacarbonyl,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17823,T3D1140,Dimanganese decacarbonyl,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17824,T3D1140,Dimanganese decacarbonyl,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17825,T3D1140,Dimanganese decacarbonyl,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17826,T3D1141,Manganese diselenide,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17827,T3D1141,Manganese diselenide,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17828,T3D1141,Manganese diselenide,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17829,T3D1141,Manganese diselenide,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17830,T3D1141,Manganese diselenide,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17831,T3D1142,Manganese heptaoxide,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17832,T3D1142,Manganese heptaoxide,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17833,T3D1142,Manganese heptaoxide,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17834,T3D1142,Manganese heptaoxide,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17835,T3D1142,Manganese heptaoxide,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17836,T3D1143,Manganese bromide,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17837,T3D1143,Manganese bromide,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17838,T3D1143,Manganese bromide,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17839,T3D1143,Manganese bromide,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17840,T3D1143,Manganese bromide,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17841,T3D1144,Manganese bromide tetrahydrate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17842,T3D1144,Manganese bromide tetrahydrate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17843,T3D1144,Manganese bromide tetrahydrate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17844,T3D1144,Manganese bromide tetrahydrate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17845,T3D1144,Manganese bromide tetrahydrate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17846,T3D1145,Manganese carbonate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17847,T3D1145,Manganese carbonate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17848,T3D1145,Manganese carbonate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17849,T3D1145,Manganese carbonate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17850,T3D1145,Manganese carbonate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17851,T3D1146,Manganese fluoride,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17852,T3D1146,Manganese fluoride,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17853,T3D1146,Manganese fluoride,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17854,T3D1146,Manganese fluoride,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17855,T3D1146,Manganese fluoride,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17856,T3D1147,Manganese phthalocyanine,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17857,T3D1147,Manganese phthalocyanine,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17858,T3D1147,Manganese phthalocyanine,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17859,T3D1147,Manganese phthalocyanine,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17860,T3D1147,Manganese phthalocyanine,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17861,T3D1148,Manganese sulfide,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17862,T3D1148,Manganese sulfide,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17863,T3D1148,Manganese sulfide,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17864,T3D1148,Manganese sulfide,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17865,T3D1148,Manganese sulfide,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17866,T3D1149,Manganese triacetate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17867,T3D1149,Manganese triacetate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17868,T3D1149,Manganese triacetate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17869,T3D1149,Manganese triacetate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17870,T3D1149,Manganese triacetate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17871,T3D1150,Manganese trifluoride,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17872,T3D1150,Manganese trifluoride,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17873,T3D1150,Manganese trifluoride,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17874,T3D1150,Manganese trifluoride,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17875,T3D1150,Manganese trifluoride,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17876,T3D1151,Manganese(III) oxide,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17877,T3D1151,Manganese(III) oxide,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17878,T3D1151,Manganese(III) oxide,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17879,T3D1151,Manganese(III) oxide,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17880,T3D1151,Manganese(III) oxide,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17881,T3D1152,Potassium manganate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17882,T3D1152,Potassium manganate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17883,T3D1152,Potassium manganate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17884,T3D1152,Potassium manganate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17885,T3D1152,Potassium manganate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17886,T3D1153,Ammonium permanganate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17887,T3D1153,Ammonium permanganate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17888,T3D1153,Ammonium permanganate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17889,T3D1153,Ammonium permanganate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17890,T3D1153,Ammonium permanganate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17891,T3D1154,Calcium permanganate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17892,T3D1154,Calcium permanganate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17893,T3D1154,Calcium permanganate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17894,T3D1154,Calcium permanganate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17895,T3D1154,Calcium permanganate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17896,T3D1155,Sodium permanganate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17897,T3D1155,Sodium permanganate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17898,T3D1155,Sodium permanganate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17899,T3D1155,Sodium permanganate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17900,T3D1155,Sodium permanganate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17901,T3D1156,Zinc permanganate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17902,T3D1156,Zinc permanganate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17903,T3D1156,Zinc permanganate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17904,T3D1156,Zinc permanganate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17905,T3D1156,Zinc permanganate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17906,T3D1157,Manganese gluconate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17907,T3D1157,Manganese gluconate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17908,T3D1157,Manganese gluconate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17909,T3D1157,Manganese gluconate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17910,T3D1157,Manganese gluconate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17911,T3D1158,Manganous acetate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17912,T3D1158,Manganous acetate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17913,T3D1158,Manganous acetate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17914,T3D1158,Manganous acetate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17915,T3D1158,Manganous acetate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17916,T3D1159,Manganese citrate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17917,T3D1159,Manganese citrate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17918,T3D1159,Manganese citrate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17919,T3D1159,Manganese citrate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17920,T3D1159,Manganese citrate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17921,T3D1119,Barium permanganate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17922,T3D1119,Barium permanganate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17923,T3D1119,Barium permanganate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17924,T3D1119,Barium permanganate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17925,T3D1119,Barium permanganate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17926,T3D1038,Flucynthrate,"Aconitate hydratase, mitochondrial",Q99798,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17927,T3D1038,Flucynthrate,Cytoplasmic aconitate hydratase,P21399,"Manganese interferes with amino acid metabolism by inhibiting aconitase, resulting in an increase in citrate levels. It is also believed that this direct disruption of the catalytic [4Fe-4S] cluster of aconitase by manganese produces iron regulary protein 1, resulting in alterations in cellular iron homeostasis. (R444)"
17928,T3D1038,Flucynthrate,Iron-responsive element-binding protein 2,P48200 ,"Manganese alters cellular iron homeostasis by stabilizing iron regulatory protein 2. This may occur by manganese competing directly for an iron-binding site on the iron binding protein, disrupting the cellular mechanisms responsible for its iron-dependent degradation. (R444)"
17929,T3D1038,Flucynthrate,Major prion protein,P04156,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17930,T3D1038,Flucynthrate,Putative testis-specific prion protein,Q86SH4,"Manganese binds to the prion protein, altering its conformation, displacing copper, and altering the redox chemistry of the metal-protein complex. These changes are similar to those associated with prion disease. (R443)"
17931,T3D1160,Ammonium diuranate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17932,T3D1161,Sodium uranate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17933,T3D1162,Triuranium octaoxide,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17934,T3D1163,Uranium dioxide,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17935,T3D1164,Uranium hexafluoride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17936,T3D1165,Uranium pentachloride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17937,T3D1166,Uranium peroxide,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17938,T3D1167,Uranium tetrachloride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17939,T3D1168,Uranium pentafluoride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17940,T3D1169,Uranium trioxide,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17941,T3D1170,Uranyl fluoride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17942,T3D1171,Uranyl nitrate hexahydrate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17943,T3D1172,Uranium boride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17944,T3D1173,Uranium carbide,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17945,T3D1174,Uranium nitride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17946,T3D1175,Uranium chloride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17947,T3D1176,Uranocene,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17948,T3D1177,Uranyl acetate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17949,T3D1178,Uranyl acetate dihydrate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17950,T3D1179,Uranyl chloride,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17951,T3D1180,Uranyl formate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17952,T3D1181,Uranyl nitrate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17953,T3D1182,Uranyl sulfate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17954,T3D1183,Uranyl zinc acetate,DNA,DNA,"Ionizing radiation produced by uranium damages the DNA, resulting in gene mutations and chromosomal aberrations. This can both both initiate and promote carcinogenesis, and interfere with reproduction and development. (R466)"
17955,T3D1184,Stryker's reagent,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17956,T3D1184,Stryker's reagent,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17957,T3D1184,Stryker's reagent,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17958,T3D1184,Stryker's reagent,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17959,T3D1184,Stryker's reagent,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17960,T3D1184,Stryker's reagent,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17961,T3D1185,Chromated copper arsenate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17962,T3D1185,Chromated copper arsenate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17963,T3D1185,Chromated copper arsenate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17964,T3D1185,Chromated copper arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
17965,T3D1185,Chromated copper arsenate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17966,T3D1185,Chromated copper arsenate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17967,T3D1186,Copper aspirinate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17968,T3D1186,Copper aspirinate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17969,T3D1186,Copper aspirinate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17970,T3D1186,Copper aspirinate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17971,T3D1186,Copper aspirinate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17972,T3D1186,Copper aspirinate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17973,T3D1187,Copper benzoate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17974,T3D1187,Copper benzoate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17975,T3D1187,Copper benzoate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17976,T3D1187,Copper benzoate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17977,T3D1187,Copper benzoate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17978,T3D1187,Copper benzoate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17979,T3D1188,Chlorophyllin,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17980,T3D1188,Chlorophyllin,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17981,T3D1188,Chlorophyllin,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17982,T3D1188,Chlorophyllin,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17983,T3D1188,Chlorophyllin,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17984,T3D1188,Chlorophyllin,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17985,T3D1189,Copper chromite,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17986,T3D1189,Copper chromite,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17987,T3D1189,Copper chromite,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17988,T3D1189,Copper chromite,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17989,T3D1189,Copper chromite,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17990,T3D1189,Copper chromite,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17991,T3D1190,Copper(I) fluoride,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17992,T3D1190,Copper(I) fluoride,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17993,T3D1190,Copper(I) fluoride,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17994,T3D1190,Copper(I) fluoride,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17995,T3D1190,Copper(I) fluoride,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17996,T3D1190,Copper(I) fluoride,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
17997,T3D1191,Copper(II) fluoride,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17998,T3D1191,Copper(II) fluoride,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
17999,T3D1191,Copper(II) fluoride,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18000,T3D1191,Copper(II) fluoride,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18001,T3D1191,Copper(II) fluoride,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18002,T3D1191,Copper(II) fluoride,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18003,T3D1192,Copper(II) fluoride dihydrate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18004,T3D1192,Copper(II) fluoride dihydrate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18005,T3D1192,Copper(II) fluoride dihydrate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18006,T3D1192,Copper(II) fluoride dihydrate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18007,T3D1192,Copper(II) fluoride dihydrate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18008,T3D1192,Copper(II) fluoride dihydrate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18009,T3D1193,Copper gluconate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18010,T3D1193,Copper gluconate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18011,T3D1193,Copper gluconate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18012,T3D1193,Copper gluconate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18013,T3D1193,Copper gluconate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18014,T3D1193,Copper gluconate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18015,T3D1194,Copper(I) oxide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18016,T3D1194,Copper(I) oxide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18017,T3D1194,Copper(I) oxide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18018,T3D1194,Copper(I) oxide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18019,T3D1194,Copper(I) oxide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18020,T3D1194,Copper(I) oxide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18021,T3D1195,Copper(II) oxide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18022,T3D1195,Copper(II) oxide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18023,T3D1195,Copper(II) oxide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18024,T3D1195,Copper(II) oxide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18025,T3D1195,Copper(II) oxide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18026,T3D1195,Copper(II) oxide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18027,T3D1196,Copper silicide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18028,T3D1196,Copper silicide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18029,T3D1196,Copper silicide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18030,T3D1196,Copper silicide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18031,T3D1196,Copper silicide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18032,T3D1196,Copper silicide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18033,T3D1197,Copper(I) sulfide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18034,T3D1197,Copper(I) sulfide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18035,T3D1197,Copper(I) sulfide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18036,T3D1197,Copper(I) sulfide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18037,T3D1197,Copper(I) sulfide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18038,T3D1197,Copper(I) sulfide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18039,T3D1198,Copper(II) sulfide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18040,T3D1198,Copper(II) sulfide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18041,T3D1198,Copper(II) sulfide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18042,T3D1198,Copper(II) sulfide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18043,T3D1198,Copper(II) sulfide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18044,T3D1198,Copper(II) sulfide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18045,T3D1199,Copper(I) acetylide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18046,T3D1199,Copper(I) acetylide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18047,T3D1199,Copper(I) acetylide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18048,T3D1199,Copper(I) acetylide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18049,T3D1199,Copper(I) acetylide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18050,T3D1199,Copper(I) acetylide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18051,T3D1200,Copper(I) bromide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18052,T3D1200,Copper(I) bromide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18053,T3D1200,Copper(I) bromide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18054,T3D1200,Copper(I) bromide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18055,T3D1200,Copper(I) bromide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18056,T3D1200,Copper(I) bromide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18057,T3D1201,Copper(I) chloride,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18058,T3D1201,Copper(I) chloride,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18059,T3D1201,Copper(I) chloride,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18060,T3D1201,Copper(I) chloride,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18061,T3D1201,Copper(I) chloride,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18062,T3D1201,Copper(I) chloride,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18063,T3D1202,Copper(I) iodide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18064,T3D1202,Copper(I) iodide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18065,T3D1202,Copper(I) iodide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18066,T3D1202,Copper(I) iodide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18067,T3D1202,Copper(I) iodide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18068,T3D1202,Copper(I) iodide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18069,T3D1203,Copper(I) phosphide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18070,T3D1203,Copper(I) phosphide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18071,T3D1203,Copper(I) phosphide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18072,T3D1203,Copper(I) phosphide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18073,T3D1203,Copper(I) phosphide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18074,T3D1203,Copper(I) phosphide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18075,T3D1204,Copper(II) acetate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18076,T3D1204,Copper(II) acetate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18077,T3D1204,Copper(II) acetate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18078,T3D1204,Copper(II) acetate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18079,T3D1204,Copper(II) acetate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18080,T3D1204,Copper(II) acetate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18081,T3D1205,Copper(II) acetate monohydrate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18082,T3D1205,Copper(II) acetate monohydrate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18083,T3D1205,Copper(II) acetate monohydrate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18084,T3D1205,Copper(II) acetate monohydrate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18085,T3D1205,Copper(II) acetate monohydrate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18086,T3D1205,Copper(II) acetate monohydrate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18087,T3D1206,Copper(II) azide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18088,T3D1206,Copper(II) azide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18089,T3D1206,Copper(II) azide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18090,T3D1206,Copper(II) azide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18091,T3D1206,Copper(II) azide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18092,T3D1206,Copper(II) azide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18093,T3D1207,Copper(II) bromide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18094,T3D1207,Copper(II) bromide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18095,T3D1207,Copper(II) bromide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18096,T3D1207,Copper(II) bromide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18097,T3D1207,Copper(II) bromide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18098,T3D1207,Copper(II) bromide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18099,T3D1208,Copper(II) carbonate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18100,T3D1208,Copper(II) carbonate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18101,T3D1208,Copper(II) carbonate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18102,T3D1208,Copper(II) carbonate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18103,T3D1208,Copper(II) carbonate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18104,T3D1208,Copper(II) carbonate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18105,T3D1209,Copper(II) chloride,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18106,T3D1209,Copper(II) chloride,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18107,T3D1209,Copper(II) chloride,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18108,T3D1209,Copper(II) chloride,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18109,T3D1209,Copper(II) chloride,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18110,T3D1209,Copper(II) chloride,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18111,T3D1210,Copper(II) chloride dihydrate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18112,T3D1210,Copper(II) chloride dihydrate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18113,T3D1210,Copper(II) chloride dihydrate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18114,T3D1210,Copper(II) chloride dihydrate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18115,T3D1210,Copper(II) chloride dihydrate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18116,T3D1210,Copper(II) chloride dihydrate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18117,T3D1211,Copper(II) hydroxide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18118,T3D1211,Copper(II) hydroxide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18119,T3D1211,Copper(II) hydroxide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18120,T3D1211,Copper(II) hydroxide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18121,T3D1211,Copper(II) hydroxide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18122,T3D1211,Copper(II) hydroxide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18123,T3D1212,Copper(II) nitrate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18124,T3D1212,Copper(II) nitrate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18125,T3D1212,Copper(II) nitrate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18126,T3D1212,Copper(II) nitrate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18127,T3D1212,Copper(II) nitrate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18128,T3D1212,Copper(II) nitrate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18129,T3D1213,Copper(II) nitrate hydrate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18130,T3D1213,Copper(II) nitrate hydrate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18131,T3D1213,Copper(II) nitrate hydrate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18132,T3D1213,Copper(II) nitrate hydrate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18133,T3D1213,Copper(II) nitrate hydrate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18134,T3D1213,Copper(II) nitrate hydrate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18135,T3D1214,Copper(II) nitrate trihydrate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18136,T3D1214,Copper(II) nitrate trihydrate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18137,T3D1214,Copper(II) nitrate trihydrate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18138,T3D1214,Copper(II) nitrate trihydrate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18139,T3D1214,Copper(II) nitrate trihydrate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18140,T3D1214,Copper(II) nitrate trihydrate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18141,T3D1215,Copper(II) sulfate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18142,T3D1215,Copper(II) sulfate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18143,T3D1215,Copper(II) sulfate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18144,T3D1215,Copper(II) sulfate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18145,T3D1215,Copper(II) sulfate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18146,T3D1215,Copper(II) sulfate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18147,T3D1216,Copper(II) sulfate pentahydrate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18148,T3D1216,Copper(II) sulfate pentahydrate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18149,T3D1216,Copper(II) sulfate pentahydrate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18150,T3D1216,Copper(II) sulfate pentahydrate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18151,T3D1216,Copper(II) sulfate pentahydrate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18152,T3D1216,Copper(II) sulfate pentahydrate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18153,T3D1217,Copper(II) triflate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18154,T3D1217,Copper(II) triflate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18155,T3D1217,Copper(II) triflate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18156,T3D1217,Copper(II) triflate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18157,T3D1217,Copper(II) triflate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18158,T3D1217,Copper(II) triflate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18159,T3D1218,Scheele's Green,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18160,T3D1218,Scheele's Green,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18161,T3D1218,Scheele's Green,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18162,T3D1218,Scheele's Green,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
18163,T3D1218,Scheele's Green,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18164,T3D1218,Scheele's Green,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18165,T3D1219,Copper(II) acetoarsenite,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18166,T3D1219,Copper(II) acetoarsenite,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18167,T3D1219,Copper(II) acetoarsenite,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18168,T3D1219,Copper(II) acetoarsenite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
18169,T3D1219,Copper(II) acetoarsenite,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18170,T3D1219,Copper(II) acetoarsenite,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18171,T3D1220,Tetramminecopper(II) sulfate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18172,T3D1220,Tetramminecopper(II) sulfate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18173,T3D1220,Tetramminecopper(II) sulfate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18174,T3D1220,Tetramminecopper(II) sulfate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18175,T3D1220,Tetramminecopper(II) sulfate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18176,T3D1220,Tetramminecopper(II) sulfate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18177,T3D1221,Copper(II) hydroxide sulfate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18178,T3D1221,Copper(II) hydroxide sulfate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18179,T3D1221,Copper(II) hydroxide sulfate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18180,T3D1221,Copper(II) hydroxide sulfate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18181,T3D1221,Copper(II) hydroxide sulfate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18182,T3D1221,Copper(II) hydroxide sulfate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18183,T3D1222,Copper orthophosphate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18184,T3D1222,Copper orthophosphate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18185,T3D1222,Copper orthophosphate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18186,T3D1222,Copper orthophosphate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18187,T3D1222,Copper orthophosphate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18188,T3D1222,Copper orthophosphate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18189,T3D1223,Copper(II) phosphate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18190,T3D1223,Copper(II) phosphate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18191,T3D1223,Copper(II) phosphate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18192,T3D1223,Copper(II) phosphate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18193,T3D1223,Copper(II) phosphate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18194,T3D1223,Copper(II) phosphate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18195,T3D1224,Copper(II) pyrophosphate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18196,T3D1224,Copper(II) pyrophosphate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18197,T3D1224,Copper(II) pyrophosphate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18198,T3D1224,Copper(II) pyrophosphate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18199,T3D1224,Copper(II) pyrophosphate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18200,T3D1224,Copper(II) pyrophosphate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18201,T3D1225,Copper chloride hydroxide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18202,T3D1225,Copper chloride hydroxide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18203,T3D1225,Copper chloride hydroxide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18204,T3D1225,Copper chloride hydroxide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18205,T3D1225,Copper chloride hydroxide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18206,T3D1225,Copper chloride hydroxide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18207,T3D1226,Copper formate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18208,T3D1226,Copper formate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18209,T3D1226,Copper formate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18210,T3D1226,Copper formate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18211,T3D1226,Copper formate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18212,T3D1226,Copper formate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18213,T3D1227,Copper tartrate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18214,T3D1227,Copper tartrate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18215,T3D1227,Copper tartrate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18216,T3D1227,Copper tartrate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18217,T3D1227,Copper tartrate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18218,T3D1227,Copper tartrate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18219,T3D1228,Copper lactate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18220,T3D1228,Copper lactate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18221,T3D1228,Copper lactate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18222,T3D1228,Copper lactate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18223,T3D1228,Copper lactate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18224,T3D1228,Copper lactate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18225,T3D1229,Copper acetylacetonate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18226,T3D1229,Copper acetylacetonate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18227,T3D1229,Copper acetylacetonate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18228,T3D1229,Copper acetylacetonate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18229,T3D1229,Copper acetylacetonate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18230,T3D1229,Copper acetylacetonate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18231,T3D1230,Copper naphthenate,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18232,T3D1230,Copper naphthenate,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18233,T3D1230,Copper naphthenate,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18234,T3D1230,Copper naphthenate,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18235,T3D1230,Copper naphthenate,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18236,T3D1230,Copper naphthenate,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18237,T3D1231,Cupriethylenediamine,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18238,T3D1231,Cupriethylenediamine,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18239,T3D1231,Cupriethylenediamine,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18240,T3D1231,Cupriethylenediamine,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18241,T3D1231,Cupriethylenediamine,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18242,T3D1231,Cupriethylenediamine,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18243,T3D0286,Copper(II) arsenite,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18244,T3D0286,Copper(II) arsenite,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18245,T3D0286,Copper(II) arsenite,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18246,T3D0286,Copper(II) arsenite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
18247,T3D0286,Copper(II) arsenite,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18248,T3D1127,Yttrium barium copper oxide,Alpha-synuclein,P37840,"Copper binds to alpha-synuclein, initiating protein aggregation and likely contributing to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18249,T3D1127,Yttrium barium copper oxide,Amyloid beta A4 protein,P05067,"Copper binds the N-terminal region of amyloid precursor protein, promoting the generation of _-amyloid from the protein. This is believed to contribute to the development of the neurodegenerative disorders Parkinson's disease and Alzheimer's disease. (R524)"
18250,T3D1127,Yttrium barium copper oxide,Glucose-6-phosphate 1-dehydrogenase,P11413,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18251,T3D1127,Yttrium barium copper oxide,"Glutathione reductase, mitochondrial",P00390,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18252,T3D1127,Yttrium barium copper oxide,Serum paraoxonase/arylesterase 1,P27169,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18253,T3D1127,Yttrium barium copper oxide,Serum paraoxonase/lactonase 3,Q15166,"Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes become saturated and copper accumulates in the nucleus, causing nuclear damage. This damage is possibly a result of oxidative damage, including lipid peroxidation. Copper inhibits the sulfhydryl group enzymes such as glucose-6-phosphate 1-dehydrogenase, glutathione reductase, and paraoxonases, which protect the cell from free oxygen radicals. It also influences gene expression and is a co-factor for oxidative enzymes such as cytochrome C oxidase and lysyl oxidase. In addition, the oxidative stress induced by copper is thought to activate acid sphingomyelinase, which lead to the production of ceramide, an apoptotic signal, as well as cause hemolytic anemia. (R513, R523, R525, R526)"
18261,T3D1238,Monomethyltin trichloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18262,T3D1238,Monomethyltin trichloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18263,T3D1238,Monomethyltin trichloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18264,T3D1238,Monomethyltin trichloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18265,T3D1238,Monomethyltin trichloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18266,T3D1238,Monomethyltin trichloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18267,T3D1238,Monomethyltin trichloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18268,T3D1238,Monomethyltin trichloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18269,T3D1238,Monomethyltin trichloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18270,T3D1238,Monomethyltin trichloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18271,T3D1238,Monomethyltin trichloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18272,T3D1238,Monomethyltin trichloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18273,T3D1239,Dimethyltin dichloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18274,T3D1239,Dimethyltin dichloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18275,T3D1239,Dimethyltin dichloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18276,T3D1239,Dimethyltin dichloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18277,T3D1239,Dimethyltin dichloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18278,T3D1239,Dimethyltin dichloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18279,T3D1239,Dimethyltin dichloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18280,T3D1239,Dimethyltin dichloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18281,T3D1239,Dimethyltin dichloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18282,T3D1239,Dimethyltin dichloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18283,T3D1239,Dimethyltin dichloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18284,T3D1239,Dimethyltin dichloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18285,T3D1240,Trimethyltin chloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18286,T3D1240,Trimethyltin chloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18287,T3D1240,Trimethyltin chloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18288,T3D1240,Trimethyltin chloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18289,T3D1240,Trimethyltin chloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18290,T3D1240,Trimethyltin chloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18291,T3D1240,Trimethyltin chloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18292,T3D1240,Trimethyltin chloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18293,T3D1240,Trimethyltin chloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18294,T3D1240,Trimethyltin chloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18295,T3D1240,Trimethyltin chloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18296,T3D1240,Trimethyltin chloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18297,T3D1241,Monobutyltin trichloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18298,T3D1241,Monobutyltin trichloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18299,T3D1241,Monobutyltin trichloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18300,T3D1241,Monobutyltin trichloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18301,T3D1241,Monobutyltin trichloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18302,T3D1241,Monobutyltin trichloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18303,T3D1241,Monobutyltin trichloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18304,T3D1241,Monobutyltin trichloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18305,T3D1241,Monobutyltin trichloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18306,T3D1241,Monobutyltin trichloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18307,T3D1241,Monobutyltin trichloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18308,T3D1241,Monobutyltin trichloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18309,T3D1242,Dibutyltin dichloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18310,T3D1242,Dibutyltin dichloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18311,T3D1242,Dibutyltin dichloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18312,T3D1242,Dibutyltin dichloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18313,T3D1242,Dibutyltin dichloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18314,T3D1242,Dibutyltin dichloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18315,T3D1242,Dibutyltin dichloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18316,T3D1242,Dibutyltin dichloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18317,T3D1242,Dibutyltin dichloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18318,T3D1242,Dibutyltin dichloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18319,T3D1242,Dibutyltin dichloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18320,T3D1242,Dibutyltin dichloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18321,T3D1244,Monobutyltin hydride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18322,T3D1244,Monobutyltin hydride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18323,T3D1244,Monobutyltin hydride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18324,T3D1244,Monobutyltin hydride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18325,T3D1244,Monobutyltin hydride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18326,T3D1244,Monobutyltin hydride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18327,T3D1244,Monobutyltin hydride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18328,T3D1244,Monobutyltin hydride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18329,T3D1244,Monobutyltin hydride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18330,T3D1244,Monobutyltin hydride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18331,T3D1244,Monobutyltin hydride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18332,T3D1244,Monobutyltin hydride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18333,T3D1245,Monobutyltin,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18334,T3D1245,Monobutyltin,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18335,T3D1245,Monobutyltin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18336,T3D1245,Monobutyltin,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18337,T3D1245,Monobutyltin,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18338,T3D1245,Monobutyltin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18339,T3D1245,Monobutyltin,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18340,T3D1245,Monobutyltin,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18341,T3D1245,Monobutyltin,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18342,T3D1245,Monobutyltin,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18343,T3D1245,Monobutyltin,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18344,T3D1245,Monobutyltin,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18345,T3D1246,Dibutyltin hydride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18346,T3D1246,Dibutyltin hydride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18347,T3D1246,Dibutyltin hydride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18348,T3D1246,Dibutyltin hydride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18349,T3D1246,Dibutyltin hydride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18350,T3D1246,Dibutyltin hydride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18351,T3D1246,Dibutyltin hydride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18352,T3D1246,Dibutyltin hydride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18353,T3D1246,Dibutyltin hydride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18354,T3D1246,Dibutyltin hydride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18355,T3D1246,Dibutyltin hydride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18356,T3D1246,Dibutyltin hydride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18357,T3D1248,Tetrabutyltin,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18358,T3D1248,Tetrabutyltin,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18359,T3D1248,Tetrabutyltin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18360,T3D1248,Tetrabutyltin,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18361,T3D1248,Tetrabutyltin,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18362,T3D1248,Tetrabutyltin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18363,T3D1248,Tetrabutyltin,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18364,T3D1248,Tetrabutyltin,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18365,T3D1248,Tetrabutyltin,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18366,T3D1248,Tetrabutyltin,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18367,T3D1248,Tetrabutyltin,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18368,T3D1248,Tetrabutyltin,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18369,T3D1250,Triethyltin bromide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18370,T3D1250,Triethyltin bromide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18371,T3D1250,Triethyltin bromide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18372,T3D1250,Triethyltin bromide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18373,T3D1250,Triethyltin bromide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18374,T3D1250,Triethyltin bromide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18375,T3D1250,Triethyltin bromide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18376,T3D1250,Triethyltin bromide,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18377,T3D1250,Triethyltin bromide,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18378,T3D1250,Triethyltin bromide,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18379,T3D1250,Triethyltin bromide,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18380,T3D1250,Triethyltin bromide,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18381,T3D1251,Triphenyltin,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18382,T3D1251,Triphenyltin,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18383,T3D1251,Triphenyltin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18384,T3D1251,Triphenyltin,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18385,T3D1251,Triphenyltin,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18386,T3D1251,Triphenyltin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18387,T3D1251,Triphenyltin,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18388,T3D1251,Triphenyltin,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18389,T3D1251,Triphenyltin,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18390,T3D1251,Triphenyltin,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18391,T3D1251,Triphenyltin,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18392,T3D1251,Triphenyltin,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18393,T3D1252,Triphenyltin hydroxide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18394,T3D1252,Triphenyltin hydroxide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18395,T3D1252,Triphenyltin hydroxide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18396,T3D1252,Triphenyltin hydroxide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18397,T3D1252,Triphenyltin hydroxide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18398,T3D1252,Triphenyltin hydroxide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18399,T3D1252,Triphenyltin hydroxide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18400,T3D1252,Triphenyltin hydroxide,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18401,T3D1252,Triphenyltin hydroxide,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18402,T3D1252,Triphenyltin hydroxide,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18403,T3D1252,Triphenyltin hydroxide,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18404,T3D1252,Triphenyltin hydroxide,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18405,T3D1253,Triphenyltin chloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18406,T3D1253,Triphenyltin chloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18407,T3D1253,Triphenyltin chloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18408,T3D1253,Triphenyltin chloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18409,T3D1253,Triphenyltin chloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18410,T3D1253,Triphenyltin chloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18411,T3D1253,Triphenyltin chloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18412,T3D1253,Triphenyltin chloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18413,T3D1253,Triphenyltin chloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18414,T3D1253,Triphenyltin chloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18415,T3D1253,Triphenyltin chloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18416,T3D1253,Triphenyltin chloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18417,T3D1254,Mono-n-octyltin trichloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18418,T3D1254,Mono-n-octyltin trichloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18419,T3D1254,Mono-n-octyltin trichloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18420,T3D1254,Mono-n-octyltin trichloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18421,T3D1254,Mono-n-octyltin trichloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18422,T3D1254,Mono-n-octyltin trichloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18423,T3D1254,Mono-n-octyltin trichloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18424,T3D1254,Mono-n-octyltin trichloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18425,T3D1254,Mono-n-octyltin trichloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18426,T3D1254,Mono-n-octyltin trichloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18427,T3D1254,Mono-n-octyltin trichloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18428,T3D1254,Mono-n-octyltin trichloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18429,T3D1255,Di-n-octyltin dichloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18430,T3D1255,Di-n-octyltin dichloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18431,T3D1255,Di-n-octyltin dichloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18432,T3D1255,Di-n-octyltin dichloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18433,T3D1255,Di-n-octyltin dichloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18434,T3D1255,Di-n-octyltin dichloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18435,T3D1255,Di-n-octyltin dichloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18436,T3D1255,Di-n-octyltin dichloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18437,T3D1255,Di-n-octyltin dichloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18438,T3D1255,Di-n-octyltin dichloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18439,T3D1255,Di-n-octyltin dichloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18440,T3D1255,Di-n-octyltin dichloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18441,T3D1256,Trioctyltin stannane,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18442,T3D1256,Trioctyltin stannane,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18443,T3D1256,Trioctyltin stannane,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18444,T3D1256,Trioctyltin stannane,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18445,T3D1256,Trioctyltin stannane,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18446,T3D1256,Trioctyltin stannane,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18447,T3D1256,Trioctyltin stannane,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18448,T3D1256,Trioctyltin stannane,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18449,T3D1256,Trioctyltin stannane,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18450,T3D1256,Trioctyltin stannane,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18451,T3D1256,Trioctyltin stannane,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18452,T3D1256,Trioctyltin stannane,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18453,T3D1257,Tri-n-octyltin chloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18454,T3D1257,Tri-n-octyltin chloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18455,T3D1257,Tri-n-octyltin chloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18456,T3D1257,Tri-n-octyltin chloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18457,T3D1257,Tri-n-octyltin chloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18458,T3D1257,Tri-n-octyltin chloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18459,T3D1257,Tri-n-octyltin chloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18460,T3D1257,Tri-n-octyltin chloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18461,T3D1257,Tri-n-octyltin chloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18462,T3D1257,Tri-n-octyltin chloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18463,T3D1257,Tri-n-octyltin chloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18464,T3D1257,Tri-n-octyltin chloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18465,T3D1258,Tetra-n-octylstannane,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18466,T3D1258,Tetra-n-octylstannane,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18467,T3D1258,Tetra-n-octylstannane,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18468,T3D1258,Tetra-n-octylstannane,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18469,T3D1258,Tetra-n-octylstannane,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18470,T3D1258,Tetra-n-octylstannane,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18471,T3D1258,Tetra-n-octylstannane,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18472,T3D1258,Tetra-n-octylstannane,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18473,T3D1258,Tetra-n-octylstannane,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18474,T3D1258,Tetra-n-octylstannane,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18475,T3D1258,Tetra-n-octylstannane,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18476,T3D1258,Tetra-n-octylstannane,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18477,T3D1259,Dibutyltin oxide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18478,T3D1259,Dibutyltin oxide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18479,T3D1259,Dibutyltin oxide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18480,T3D1259,Dibutyltin oxide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18481,T3D1259,Dibutyltin oxide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18482,T3D1259,Dibutyltin oxide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18483,T3D1259,Dibutyltin oxide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18484,T3D1259,Dibutyltin oxide,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18485,T3D1259,Dibutyltin oxide,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18486,T3D1259,Dibutyltin oxide,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18487,T3D1259,Dibutyltin oxide,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18488,T3D1259,Dibutyltin oxide,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18489,T3D1260,Fentin acetate,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18490,T3D1260,Fentin acetate,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18491,T3D1260,Fentin acetate,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18492,T3D1260,Fentin acetate,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18493,T3D1260,Fentin acetate,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18494,T3D1260,Fentin acetate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18495,T3D1260,Fentin acetate,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18496,T3D1260,Fentin acetate,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18497,T3D1260,Fentin acetate,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18498,T3D1260,Fentin acetate,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18499,T3D1260,Fentin acetate,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18500,T3D1260,Fentin acetate,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18501,T3D1261,Tetraethyltin,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18502,T3D1261,Tetraethyltin,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18503,T3D1261,Tetraethyltin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18504,T3D1261,Tetraethyltin,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18505,T3D1261,Tetraethyltin,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18506,T3D1261,Tetraethyltin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18507,T3D1261,Tetraethyltin,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18508,T3D1261,Tetraethyltin,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18509,T3D1261,Tetraethyltin,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18510,T3D1261,Tetraethyltin,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18511,T3D1261,Tetraethyltin,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18512,T3D1261,Tetraethyltin,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18513,T3D1262,Tetramethyltin,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18514,T3D1262,Tetramethyltin,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18515,T3D1262,Tetramethyltin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18516,T3D1262,Tetramethyltin,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18517,T3D1262,Tetramethyltin,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18518,T3D1262,Tetramethyltin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18519,T3D1262,Tetramethyltin,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18520,T3D1262,Tetramethyltin,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18521,T3D1262,Tetramethyltin,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18522,T3D1262,Tetramethyltin,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18523,T3D1262,Tetramethyltin,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18524,T3D1262,Tetramethyltin,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18525,T3D1263,Triphenyltin hydride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18526,T3D1263,Triphenyltin hydride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18527,T3D1263,Triphenyltin hydride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18528,T3D1263,Triphenyltin hydride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18529,T3D1263,Triphenyltin hydride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18530,T3D1263,Triphenyltin hydride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18531,T3D1263,Triphenyltin hydride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18532,T3D1263,Triphenyltin hydride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18533,T3D1263,Triphenyltin hydride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18534,T3D1263,Triphenyltin hydride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18535,T3D1263,Triphenyltin hydride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18536,T3D1263,Triphenyltin hydride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18537,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18538,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18539,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18540,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18541,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18542,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18543,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18544,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18545,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18546,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18547,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18548,T3D1280,Monomethyltin tris(isooctyl mercaptoacetate),Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18549,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18550,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18551,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18552,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18553,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18554,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18555,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18556,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18557,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18558,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18559,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18560,T3D1281,Dimethyltin bis(isooctyl mercaptoacetate),Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18561,T3D1282,Dibutyltin diacetate,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18562,T3D1282,Dibutyltin diacetate,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18563,T3D1282,Dibutyltin diacetate,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18564,T3D1282,Dibutyltin diacetate,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18565,T3D1282,Dibutyltin diacetate,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18566,T3D1282,Dibutyltin diacetate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18567,T3D1282,Dibutyltin diacetate,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18568,T3D1282,Dibutyltin diacetate,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18569,T3D1282,Dibutyltin diacetate,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18570,T3D1282,Dibutyltin diacetate,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18571,T3D1282,Dibutyltin diacetate,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18572,T3D1282,Dibutyltin diacetate,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18573,T3D1283,Dibutyltin dilaurate,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18574,T3D1283,Dibutyltin dilaurate,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18575,T3D1283,Dibutyltin dilaurate,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18576,T3D1283,Dibutyltin dilaurate,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18577,T3D1283,Dibutyltin dilaurate,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18578,T3D1283,Dibutyltin dilaurate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18579,T3D1283,Dibutyltin dilaurate,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18580,T3D1283,Dibutyltin dilaurate,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18581,T3D1283,Dibutyltin dilaurate,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18582,T3D1283,Dibutyltin dilaurate,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18583,T3D1283,Dibutyltin dilaurate,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18584,T3D1283,Dibutyltin dilaurate,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18585,T3D1284,Tricyclohexyltin hydroxide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18586,T3D1284,Tricyclohexyltin hydroxide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18587,T3D1284,Tricyclohexyltin hydroxide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18588,T3D1284,Tricyclohexyltin hydroxide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18589,T3D1284,Tricyclohexyltin hydroxide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18590,T3D1284,Tricyclohexyltin hydroxide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18591,T3D1284,Tricyclohexyltin hydroxide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18592,T3D1284,Tricyclohexyltin hydroxide,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18593,T3D1284,Tricyclohexyltin hydroxide,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18594,T3D1284,Tricyclohexyltin hydroxide,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18595,T3D1284,Tricyclohexyltin hydroxide,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18596,T3D1284,Tricyclohexyltin hydroxide,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18597,T3D1285,Azocyclotin,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18598,T3D1285,Azocyclotin,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18599,T3D1285,Azocyclotin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18600,T3D1285,Azocyclotin,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18601,T3D1285,Azocyclotin,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18602,T3D1285,Azocyclotin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18603,T3D1285,Azocyclotin,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18604,T3D1285,Azocyclotin,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18605,T3D1285,Azocyclotin,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18606,T3D1285,Azocyclotin,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18607,T3D1285,Azocyclotin,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18608,T3D1285,Azocyclotin,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18609,T3D1286,Fenbutatin oxide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18610,T3D1286,Fenbutatin oxide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18611,T3D1286,Fenbutatin oxide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18612,T3D1286,Fenbutatin oxide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18613,T3D1286,Fenbutatin oxide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18614,T3D1286,Fenbutatin oxide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18615,T3D1286,Fenbutatin oxide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18616,T3D1286,Fenbutatin oxide,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18617,T3D1286,Fenbutatin oxide,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18618,T3D1286,Fenbutatin oxide,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18619,T3D1286,Fenbutatin oxide,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18620,T3D1286,Fenbutatin oxide,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18642,T3D1232,Tin(II) chloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18643,T3D1232,Tin(II) chloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18644,T3D1232,Tin(II) chloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18645,T3D1232,Tin(II) chloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18646,T3D1232,Tin(II) chloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18647,T3D1232,Tin(II) chloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18648,T3D1232,Tin(II) chloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18649,T3D1233,Tin(II) chloride dihydrate,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18650,T3D1233,Tin(II) chloride dihydrate,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18651,T3D1233,Tin(II) chloride dihydrate,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18652,T3D1233,Tin(II) chloride dihydrate,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18653,T3D1233,Tin(II) chloride dihydrate,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18654,T3D1233,Tin(II) chloride dihydrate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18655,T3D1233,Tin(II) chloride dihydrate,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18656,T3D1234,Tin(IV) oxide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18657,T3D1234,Tin(IV) oxide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18658,T3D1234,Tin(IV) oxide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18659,T3D1234,Tin(IV) oxide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18660,T3D1234,Tin(IV) oxide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18661,T3D1234,Tin(IV) oxide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18662,T3D1234,Tin(IV) oxide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18663,T3D1235,Tin(IV) oxide monohydrate,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18664,T3D1235,Tin(IV) oxide monohydrate,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18665,T3D1235,Tin(IV) oxide monohydrate,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18666,T3D1235,Tin(IV) oxide monohydrate,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18667,T3D1235,Tin(IV) oxide monohydrate,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18668,T3D1235,Tin(IV) oxide monohydrate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18669,T3D1235,Tin(IV) oxide monohydrate,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18670,T3D1236,Tin(II) fluoroborate,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18671,T3D1236,Tin(II) fluoroborate,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18672,T3D1236,Tin(II) fluoroborate,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18673,T3D1236,Tin(II) fluoroborate,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18674,T3D1236,Tin(II) fluoroborate,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18675,T3D1236,Tin(II) fluoroborate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18676,T3D1236,Tin(II) fluoroborate,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18677,T3D1237,Tin(II) fluoride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18678,T3D1237,Tin(II) fluoride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18679,T3D1237,Tin(II) fluoride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18680,T3D1237,Tin(II) fluoride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18681,T3D1237,Tin(II) fluoride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18682,T3D1237,Tin(II) fluoride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18683,T3D1237,Tin(II) fluoride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18684,T3D1264,Niobium tin,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18685,T3D1264,Niobium tin,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18686,T3D1264,Niobium tin,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18687,T3D1264,Niobium tin,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18688,T3D1264,Niobium tin,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18689,T3D1264,Niobium tin,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18690,T3D1264,Niobium tin,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18691,T3D1265,Stannane,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18692,T3D1265,Stannane,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18693,T3D1265,Stannane,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18694,T3D1265,Stannane,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18695,T3D1265,Stannane,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18696,T3D1265,Stannane,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18697,T3D1265,Stannane,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18698,T3D1266,Tin selenide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18699,T3D1266,Tin selenide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18700,T3D1266,Tin selenide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18701,T3D1266,Tin selenide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18702,T3D1266,Tin selenide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18703,T3D1266,Tin selenide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18704,T3D1266,Tin selenide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18705,T3D1267,Tin telluride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18706,T3D1267,Tin telluride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18707,T3D1267,Tin telluride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18708,T3D1267,Tin telluride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18709,T3D1267,Tin telluride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18710,T3D1267,Tin telluride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18711,T3D1267,Tin telluride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18712,T3D1268,Tin(II) bromide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18713,T3D1268,Tin(II) bromide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18714,T3D1268,Tin(II) bromide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18715,T3D1268,Tin(II) bromide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18716,T3D1268,Tin(II) bromide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18717,T3D1268,Tin(II) bromide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18718,T3D1268,Tin(II) bromide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18719,T3D1269,Tin(II) hydroxide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18720,T3D1269,Tin(II) hydroxide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18721,T3D1269,Tin(II) hydroxide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18722,T3D1269,Tin(II) hydroxide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18723,T3D1269,Tin(II) hydroxide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18724,T3D1269,Tin(II) hydroxide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18725,T3D1269,Tin(II) hydroxide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18726,T3D1270,Tin(II) iodide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18727,T3D1270,Tin(II) iodide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18728,T3D1270,Tin(II) iodide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18729,T3D1270,Tin(II) iodide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18730,T3D1270,Tin(II) iodide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18731,T3D1270,Tin(II) iodide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18732,T3D1270,Tin(II) iodide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18733,T3D1271,Tin(II) oxide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18734,T3D1271,Tin(II) oxide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18735,T3D1271,Tin(II) oxide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18736,T3D1271,Tin(II) oxide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18737,T3D1271,Tin(II) oxide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18738,T3D1271,Tin(II) oxide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18739,T3D1271,Tin(II) oxide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18740,T3D1272,Tin(II) sulfate,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18741,T3D1272,Tin(II) sulfate,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18742,T3D1272,Tin(II) sulfate,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18743,T3D1272,Tin(II) sulfate,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18744,T3D1272,Tin(II) sulfate,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18745,T3D1272,Tin(II) sulfate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18746,T3D1272,Tin(II) sulfate,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18747,T3D1273,Tin(II) sulfide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18748,T3D1273,Tin(II) sulfide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18749,T3D1273,Tin(II) sulfide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18750,T3D1273,Tin(II) sulfide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18751,T3D1273,Tin(II) sulfide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18752,T3D1273,Tin(II) sulfide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18753,T3D1273,Tin(II) sulfide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18754,T3D1274,Tin(IV) bromide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18755,T3D1274,Tin(IV) bromide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18756,T3D1274,Tin(IV) bromide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18757,T3D1274,Tin(IV) bromide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18758,T3D1274,Tin(IV) bromide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18759,T3D1274,Tin(IV) bromide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18760,T3D1274,Tin(IV) bromide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18761,T3D1275,Tin(IV) chloride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18762,T3D1275,Tin(IV) chloride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18763,T3D1275,Tin(IV) chloride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18764,T3D1275,Tin(IV) chloride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18765,T3D1275,Tin(IV) chloride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18766,T3D1275,Tin(IV) chloride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18767,T3D1275,Tin(IV) chloride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18768,T3D1276,Tin(IV) chloride pentahydrate,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18769,T3D1276,Tin(IV) chloride pentahydrate,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18770,T3D1276,Tin(IV) chloride pentahydrate,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18771,T3D1276,Tin(IV) chloride pentahydrate,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18772,T3D1276,Tin(IV) chloride pentahydrate,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18773,T3D1276,Tin(IV) chloride pentahydrate,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18774,T3D1276,Tin(IV) chloride pentahydrate,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18775,T3D1277,Tin(IV) fluoride,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18776,T3D1277,Tin(IV) fluoride,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18777,T3D1277,Tin(IV) fluoride,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18778,T3D1277,Tin(IV) fluoride,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18779,T3D1277,Tin(IV) fluoride,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18780,T3D1277,Tin(IV) fluoride,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18781,T3D1277,Tin(IV) fluoride,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18782,T3D1278,Tin(IV) iodide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18783,T3D1278,Tin(IV) iodide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18784,T3D1278,Tin(IV) iodide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18785,T3D1278,Tin(IV) iodide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18786,T3D1278,Tin(IV) iodide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18787,T3D1278,Tin(IV) iodide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18788,T3D1278,Tin(IV) iodide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18789,T3D1279,Tin(IV) sulfide,Alcohol dehydrogenase 1A,P07327,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18790,T3D1279,Tin(IV) sulfide,Alcohol dehydrogenase 1B,P00325,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18791,T3D1279,Tin(IV) sulfide,Alcohol dehydrogenase 1C,P00326,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18792,T3D1279,Tin(IV) sulfide,Alcohol dehydrogenase 4,P08319,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18793,T3D1279,Tin(IV) sulfide,Alcohol dehydrogenase 6,P28332,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18794,T3D1279,Tin(IV) sulfide,Alcohol dehydrogenase class 4 mu/sigma chain,P40394,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18795,T3D1279,Tin(IV) sulfide,Alcohol dehydrogenase class-3,P11766,Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (R570)
18796,T3D1243,Tributyltin chloride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18797,T3D1243,Tributyltin chloride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18798,T3D1243,Tributyltin chloride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18799,T3D1243,Tributyltin chloride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18800,T3D1243,Tributyltin chloride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18801,T3D1243,Tributyltin chloride,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18802,T3D1243,Tributyltin chloride,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18803,T3D1243,Tributyltin chloride,Thioredoxin reductase 3,Q86VQ6,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18804,T3D1247,Tributyltin hydride,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18805,T3D1247,Tributyltin hydride,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18806,T3D1247,Tributyltin hydride,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18807,T3D1247,Tributyltin hydride,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18808,T3D1247,Tributyltin hydride,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18809,T3D1247,Tributyltin hydride,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18810,T3D1247,Tributyltin hydride,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18811,T3D1247,Tributyltin hydride,Thioredoxin reductase 3,Q86VQ6,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18812,T3D1287,Tributyltin methacrylate,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18813,T3D1287,Tributyltin methacrylate,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18814,T3D1287,Tributyltin methacrylate,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18815,T3D1287,Tributyltin methacrylate,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18816,T3D1287,Tributyltin methacrylate,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18817,T3D1287,Tributyltin methacrylate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18818,T3D1287,Tributyltin methacrylate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18819,T3D1287,Tributyltin methacrylate,Thioredoxin reductase 3,Q86VQ6,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18820,T3D1249,Bis(tributyltin) oxide,Peroxisome proliferator-activated receptor gamma,P37231,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of peroxisome proliferator-activated receptor gamma, leading to adipocyte differentiation. (R571)"
18821,T3D1249,Bis(tributyltin) oxide,Proteasome subunit beta type-5,P28074,Organotins inhibit the chymotrypsin-like activity of 20S and cellular proteasomes by binding to the beta-5 subunit. This results in apoptosis caused by downstream effects in the proteasome pathway. (R567)
18822,T3D1249,Bis(tributyltin) oxide,Retinoic acid receptor alpha,P10276,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18823,T3D1249,Bis(tributyltin) oxide,Retinoic acid receptor beta,P10826,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18824,T3D1249,Bis(tributyltin) oxide,Retinoic acid receptor gamma-1,P13631,"Organotins are endocrine disruptors and are believed to contribute to obesity by inappropriate activation of retinoic acid receptors, leading to adipocyte differentiation. (R571)"
18825,T3D1249,Bis(tributyltin) oxide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18826,T3D1249,Bis(tributyltin) oxide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18827,T3D1249,Bis(tributyltin) oxide,Thioredoxin reductase 3,Q86VQ6,"Tributyltin inhibits thioredoxin reductase, leading to hydrogen peroxide production. (R572)"
18828,T3D1486,Aluminium chlorohydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18829,T3D1486,Aluminium chlorohydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18830,T3D1486,Aluminium chlorohydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18831,T3D1487,Aluminium diacetate hydroxide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18832,T3D1487,Aluminium diacetate hydroxide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18833,T3D1487,Aluminium diacetate hydroxide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18834,T3D1488,Aluminum triacetate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18835,T3D1488,Aluminum triacetate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18836,T3D1488,Aluminum triacetate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18837,T3D1489,Aloglutamol,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18838,T3D1489,Aloglutamol,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18839,T3D1489,Aloglutamol,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18840,T3D1490,Aluminium acetoacetate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18841,T3D1490,Aluminium acetoacetate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18842,T3D1490,Aluminium acetoacetate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18843,T3D1491,Aluminium antimonide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18844,T3D1491,Aluminium antimonide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18845,T3D1491,Aluminium antimonide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18846,T3D1492,Aluminium carbide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18847,T3D1492,Aluminium carbide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18848,T3D1492,Aluminium carbide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18849,T3D1493,Aluminium chloride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18850,T3D1493,Aluminium chloride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18851,T3D1493,Aluminium chloride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18852,T3D1494,Aluminium chloride hexahydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18853,T3D1494,Aluminium chloride hexahydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18854,T3D1494,Aluminium chloride hexahydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18855,T3D1495,Aluminium diboride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18856,T3D1495,Aluminium diboride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18857,T3D1495,Aluminium diboride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18858,T3D1496,Aluminium dodecaboride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18859,T3D1496,Aluminium dodecaboride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18860,T3D1496,Aluminium dodecaboride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18861,T3D1497,Aluminium lactate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18862,T3D1497,Aluminium lactate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18863,T3D1497,Aluminium lactate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18864,T3D1498,Aluminium fluoride monohydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18865,T3D1498,Aluminium fluoride monohydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18866,T3D1498,Aluminium fluoride monohydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18867,T3D1499,Potassium aluminium fluoride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18868,T3D1499,Potassium aluminium fluoride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18869,T3D1499,Potassium aluminium fluoride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18870,T3D1500,Aluminium fluoride trihydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18871,T3D1500,Aluminium fluoride trihydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18872,T3D1500,Aluminium fluoride trihydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18873,T3D1501,Aluminium glycinate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18874,T3D1501,Aluminium glycinate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18875,T3D1501,Aluminium glycinate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18876,T3D1502,Aluminium hydride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18877,T3D1502,Aluminium hydride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18878,T3D1502,Aluminium hydride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18879,T3D1503,Lithium aluminium hydride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18880,T3D1503,Lithium aluminium hydride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18881,T3D1503,Lithium aluminium hydride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18882,T3D1504,Aluminium hydroxide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18883,T3D1504,Aluminium hydroxide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18884,T3D1504,Aluminium hydroxide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18885,T3D1505,Aluminium iodide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18886,T3D1505,Aluminium iodide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18887,T3D1505,Aluminium iodide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18888,T3D1506,Aluminium iodide hexahydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18889,T3D1506,Aluminium iodide hexahydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18890,T3D1506,Aluminium iodide hexahydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18891,T3D1507,Aluminium(I) oxide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18892,T3D1507,Aluminium(I) oxide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18893,T3D1507,Aluminium(I) oxide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18894,T3D1508,Aluminium(II) oxide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18895,T3D1508,Aluminium(II) oxide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18896,T3D1508,Aluminium(II) oxide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18897,T3D1509,Aluminium(III) oxide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18898,T3D1509,Aluminium(III) oxide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18899,T3D1509,Aluminium(III) oxide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18900,T3D1510,Aluminium isopropoxide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18901,T3D1510,Aluminium isopropoxide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18902,T3D1510,Aluminium isopropoxide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18903,T3D1511,Aluminium molybdate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18904,T3D1511,Aluminium molybdate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18905,T3D1511,Aluminium molybdate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18906,T3D1512,Aluminium monochloride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18907,T3D1512,Aluminium monochloride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18908,T3D1512,Aluminium monochloride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18909,T3D1513,Aluminium monofluoride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18910,T3D1513,Aluminium monofluoride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18911,T3D1513,Aluminium monofluoride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18912,T3D1514,Aluminium monostearate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18913,T3D1514,Aluminium monostearate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18914,T3D1514,Aluminium monostearate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18915,T3D1515,Aluminium nitrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18916,T3D1515,Aluminium nitrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18917,T3D1515,Aluminium nitrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18918,T3D1516,Aluminium nitrate hexahydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18919,T3D1516,Aluminium nitrate hexahydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18920,T3D1516,Aluminium nitrate hexahydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18921,T3D1517,Aluminium nitride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18922,T3D1517,Aluminium nitride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18923,T3D1517,Aluminium nitride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18924,T3D1518,Aluminium oxynitride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18925,T3D1518,Aluminium oxynitride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18926,T3D1518,Aluminium oxynitride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18927,T3D1519,Aluminium phosphate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18928,T3D1519,Aluminium phosphate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18929,T3D1519,Aluminium phosphate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18930,T3D1520,Aluminium phosphide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18931,T3D1520,Aluminium phosphide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18932,T3D1520,Aluminium phosphide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18933,T3D1521,Aluminium silicate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18934,T3D1521,Aluminium silicate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18935,T3D1521,Aluminium silicate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18936,T3D1522,Aluminium sulfate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18937,T3D1522,Aluminium sulfate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18938,T3D1522,Aluminium sulfate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18939,T3D1523,Aluminium sulfate octadecahydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18940,T3D1523,Aluminium sulfate octadecahydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18941,T3D1523,Aluminium sulfate octadecahydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18942,T3D1524,Aluminium sulfide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18943,T3D1524,Aluminium sulfide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18944,T3D1524,Aluminium sulfide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18945,T3D1525,Methylaluminoxane,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18946,T3D1525,Methylaluminoxane,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18947,T3D1525,Methylaluminoxane,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18948,T3D1526,Aluminum ammonium sulfate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18949,T3D1526,Aluminum ammonium sulfate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18950,T3D1526,Aluminum ammonium sulfate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18951,T3D1527,Aluminum ammonium sulfate dodecahydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18952,T3D1527,Aluminum ammonium sulfate dodecahydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18953,T3D1527,Aluminum ammonium sulfate dodecahydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18954,T3D1528,Diisobutylaluminium hydride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18955,T3D1528,Diisobutylaluminium hydride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18956,T3D1528,Diisobutylaluminium hydride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18957,T3D1529,Potassium alum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18958,T3D1529,Potassium alum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18959,T3D1529,Potassium alum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18960,T3D1530,Potassium alum dodecahydrate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18961,T3D1530,Potassium alum dodecahydrate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18962,T3D1530,Potassium alum dodecahydrate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18963,T3D1531,Sodium bis(2-methoxyethoxy)aluminumhydride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18964,T3D1531,Sodium bis(2-methoxyethoxy)aluminumhydride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18965,T3D1531,Sodium bis(2-methoxyethoxy)aluminumhydride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18966,T3D1532,Sodium aluminium hydride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18967,T3D1532,Sodium aluminium hydride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18968,T3D1532,Sodium aluminium hydride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18969,T3D1533,Sodium hexafluoroaluminate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18970,T3D1533,Sodium hexafluoroaluminate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18971,T3D1533,Sodium hexafluoroaluminate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18972,T3D1534,Tebbe's reagent,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18973,T3D1534,Tebbe's reagent,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18974,T3D1534,Tebbe's reagent,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18975,T3D1535,Triethylaluminium,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18976,T3D1535,Triethylaluminium,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18977,T3D1535,Triethylaluminium,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18978,T3D1536,Trimethylaluminium,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18979,T3D1536,Trimethylaluminium,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18980,T3D1536,Trimethylaluminium,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18981,T3D1537,Tris(8-hydroxyquinolinato)aluminium,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18982,T3D1537,Tris(8-hydroxyquinolinato)aluminium,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18983,T3D1537,Tris(8-hydroxyquinolinato)aluminium,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18984,T3D1538,Lithium aluminate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18985,T3D1538,Lithium aluminate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18986,T3D1538,Lithium aluminate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18987,T3D1539,Sodium aluminate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18988,T3D1539,Sodium aluminate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18989,T3D1539,Sodium aluminate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18990,T3D1540,Strontium aluminate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18991,T3D1540,Strontium aluminate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18992,T3D1540,Strontium aluminate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18993,T3D1541,Magnesium aluminate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18994,T3D1541,Magnesium aluminate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18995,T3D1541,Magnesium aluminate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18996,T3D1542,Tantalum(III) aluminide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
18997,T3D1542,Tantalum(III) aluminide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
18998,T3D1542,Tantalum(III) aluminide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
18999,T3D1543,Titanium aluminide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19000,T3D1543,Titanium aluminide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19001,T3D1543,Titanium aluminide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19002,T3D1544,Lithium tetrachloroaluminate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19003,T3D1544,Lithium tetrachloroaluminate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19004,T3D1544,Lithium tetrachloroaluminate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19005,T3D1545,Dichloroethylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19006,T3D1545,Dichloroethylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19007,T3D1545,Dichloroethylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19008,T3D1546,Aluminum sodium sulfate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19009,T3D1546,Aluminum sodium sulfate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19010,T3D1546,Aluminum sodium sulfate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19011,T3D1547,Aluminum palmitate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19012,T3D1547,Aluminum palmitate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19013,T3D1547,Aluminum palmitate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19014,T3D1548,Aluminum oleate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19015,T3D1548,Aluminum oleate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19016,T3D1548,Aluminum oleate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19017,T3D1549,Sodium aluminum phosphate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19018,T3D1549,Sodium aluminum phosphate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19019,T3D1549,Sodium aluminum phosphate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19020,T3D1550,Triisobutylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19021,T3D1550,Triisobutylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19022,T3D1550,Triisobutylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19023,T3D1551,Ethylaluminum sesquichloride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19024,T3D1551,Ethylaluminum sesquichloride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19025,T3D1551,Ethylaluminum sesquichloride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19026,T3D1552,Methyl aluminum sesquibromide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19027,T3D1552,Methyl aluminum sesquibromide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19028,T3D1552,Methyl aluminum sesquibromide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19029,T3D1553,Chlorodiethyaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19030,T3D1553,Chlorodiethyaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19031,T3D1553,Chlorodiethyaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19032,T3D1554,Aluminum ethylate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19033,T3D1554,Aluminum ethylate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19034,T3D1554,Aluminum ethylate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19035,T3D1555,Aluminum distearate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19036,T3D1555,Aluminum distearate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19037,T3D1555,Aluminum distearate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19038,T3D1556,Aluminum tristearate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19039,T3D1556,Aluminum tristearate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19040,T3D1556,Aluminum tristearate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19041,T3D1557,Tri-n-ocylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19042,T3D1557,Tri-n-ocylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19043,T3D1557,Tri-n-ocylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19044,T3D1558,Tri-n-butylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19045,T3D1558,Tri-n-butylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19046,T3D1558,Tri-n-butylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19047,T3D1559,Tri-n-hexylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19048,T3D1559,Tri-n-hexylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19049,T3D1559,Tri-n-hexylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19050,T3D1560,Trieicosylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19051,T3D1560,Trieicosylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19052,T3D1560,Trieicosylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19053,T3D1561,Tritetradecylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19054,T3D1561,Tritetradecylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19055,T3D1561,Tritetradecylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19056,T3D1562,Tris(dodecyl)aluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19057,T3D1562,Tris(dodecyl)aluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19058,T3D1562,Tris(dodecyl)aluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19059,T3D1563,Trihexadecylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19060,T3D1563,Trihexadecylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19061,T3D1563,Trihexadecylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19062,T3D1564,Tri-n-decylaluminum,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19063,T3D1564,Tri-n-decylaluminum,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19064,T3D1564,Tri-n-decylaluminum,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19065,T3D1565,Bis(isobutyl)aluminum chloride,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19066,T3D1565,Bis(isobutyl)aluminum chloride,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19067,T3D1565,Bis(isobutyl)aluminum chloride,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19068,T3D1566,Aluminum calcium sodium silicate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19069,T3D1566,Aluminum calcium sodium silicate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19070,T3D1566,Aluminum calcium sodium silicate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19071,T3D1567,"Aluminum oxide hydroxide, alpha-",Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19072,T3D1567,"Aluminum oxide hydroxide, alpha-","NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19073,T3D1567,"Aluminum oxide hydroxide, alpha-",Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19074,T3D1568,"Aluminum oxide hydroxide, gamma-",Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19075,T3D1568,"Aluminum oxide hydroxide, gamma-","NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19076,T3D1568,"Aluminum oxide hydroxide, gamma-",Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19077,T3D1569,"Aluminum oxide trihydrate, alpha-",Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19078,T3D1569,"Aluminum oxide trihydrate, alpha-","NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19079,T3D1569,"Aluminum oxide trihydrate, alpha-",Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19080,T3D1570,"Aluminum oxide trihydrate, beta-",Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19081,T3D1570,"Aluminum oxide trihydrate, beta-","NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19082,T3D1570,"Aluminum oxide trihydrate, beta-",Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19083,T3D1571,Aluminum butylate,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19084,T3D1571,Aluminum butylate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19085,T3D1571,Aluminum butylate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19086,T3D1091,Aluminium barium titanium oxide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19087,T3D1091,Aluminium barium titanium oxide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19088,T3D1091,Aluminium barium titanium oxide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19089,T3D1289,Aluminium arsenide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
19090,T3D1289,Aluminium arsenide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19091,T3D1289,Aluminium arsenide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19092,T3D1374,Cadmium(I) tetrachloroaluminate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
19093,T3D1374,Cadmium(I) tetrachloroaluminate,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19094,T3D1374,Cadmium(I) tetrachloroaluminate,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19095,T3D1414,Nickel aluminide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19096,T3D1414,Nickel aluminide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19097,T3D1414,Nickel aluminide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19098,T3D1720,Aluminium bromide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19099,T3D1720,Aluminium bromide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19100,T3D1720,Aluminium bromide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19101,T3D1828,Aluminium selenide,Estrogen receptor,P03372,"Aluminum can also interact with estrogen receptors, increasing the expression of estrogen-related genes and contributing to the progression of breast cancer. (R1130)"
19102,T3D1828,Aluminium selenide,"NACHT, LRR and PYD domains-containing protein 3",Q96P20,"Certain aluminum salts induce immune responses by activating the NALP3 inflammasome, which in turn induces the production of interleukins. (R1132)"
19103,T3D1828,Aluminium selenide,Phosphorus,Phosphorus,Aluminum binds with dietary phosphorus and impairs gastrointestinal absorption of phosphorus. The decreased phosphate body burden results in osteomalacia (softening of the bones due to defective bone mineralization) and rickets. (R1128)
19104,T3D1572,Allylpalladium chloride dimer,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19105,T3D1572,Allylpalladium chloride dimer,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19106,T3D1572,Allylpalladium chloride dimer,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19107,T3D1572,Allylpalladium chloride dimer,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19108,T3D1572,Allylpalladium chloride dimer,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19109,T3D1573,Palladium acetylacetonate,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19110,T3D1573,Palladium acetylacetonate,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19111,T3D1573,Palladium acetylacetonate,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19112,T3D1573,Palladium acetylacetonate,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19113,T3D1573,Palladium acetylacetonate,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19114,T3D1574,Palladium hydride,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19115,T3D1574,Palladium hydride,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19116,T3D1574,Palladium hydride,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19117,T3D1574,Palladium hydride,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19118,T3D1574,Palladium hydride,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19119,T3D1575,Palladium(II) acetate,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19120,T3D1575,Palladium(II) acetate,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19121,T3D1575,Palladium(II) acetate,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19122,T3D1575,Palladium(II) acetate,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19123,T3D1575,Palladium(II) acetate,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19124,T3D1576,Palladium(II) chloride,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19125,T3D1576,Palladium(II) chloride,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19126,T3D1576,Palladium(II) chloride,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19127,T3D1576,Palladium(II) chloride,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19128,T3D1576,Palladium(II) chloride,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19129,T3D1577,Palladium(II) nitrate,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19130,T3D1577,Palladium(II) nitrate,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19131,T3D1577,Palladium(II) nitrate,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19132,T3D1577,Palladium(II) nitrate,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19133,T3D1577,Palladium(II) nitrate,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19134,T3D1578,Palladium(II) oxide,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19135,T3D1578,Palladium(II) oxide,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19136,T3D1578,Palladium(II) oxide,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19137,T3D1578,Palladium(II) oxide,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19138,T3D1578,Palladium(II) oxide,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19139,T3D1579,Tetrakis(triphenylphosphine)palladium(0),Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19140,T3D1579,Tetrakis(triphenylphosphine)palladium(0),Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19141,T3D1579,Tetrakis(triphenylphosphine)palladium(0),Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19142,T3D1579,Tetrakis(triphenylphosphine)palladium(0),Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19143,T3D1579,Tetrakis(triphenylphosphine)palladium(0),Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19144,T3D1580,Tris(dibenzylideneacetone)dipalladium(0),Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19145,T3D1580,Tris(dibenzylideneacetone)dipalladium(0),Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19146,T3D1580,Tris(dibenzylideneacetone)dipalladium(0),Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19147,T3D1580,Tris(dibenzylideneacetone)dipalladium(0),Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19148,T3D1580,Tris(dibenzylideneacetone)dipalladium(0),Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19149,T3D1581,Ammonium hexachloro-palladate(IV),Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19150,T3D1581,Ammonium hexachloro-palladate(IV),Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19151,T3D1581,Ammonium hexachloro-palladate(IV),Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19152,T3D1581,Ammonium hexachloro-palladate(IV),Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19153,T3D1581,Ammonium hexachloro-palladate(IV),Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19154,T3D1582,Ammonium tetrachloro-palladate(II),Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19155,T3D1582,Ammonium tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19156,T3D1582,Ammonium tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19157,T3D1582,Ammonium tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19158,T3D1582,Ammonium tetrachloro-palladate(II),Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19159,T3D1583,"Bis(1,5-diphenyl-1,4-pentadien-3-one) palladium(0)",Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19160,T3D1583,"Bis(1,5-diphenyl-1,4-pentadien-3-one) palladium(0)",Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19161,T3D1583,"Bis(1,5-diphenyl-1,4-pentadien-3-one) palladium(0)",Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19162,T3D1583,"Bis(1,5-diphenyl-1,4-pentadien-3-one) palladium(0)",Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19163,T3D1583,"Bis(1,5-diphenyl-1,4-pentadien-3-one) palladium(0)",Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19164,T3D1584,"Bis(2,4-pentanedionato) palladium(II)",Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19165,T3D1584,"Bis(2,4-pentanedionato) palladium(II)",Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19166,T3D1584,"Bis(2,4-pentanedionato) palladium(II)",Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19167,T3D1584,"Bis(2,4-pentanedionato) palladium(II)",Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19168,T3D1584,"Bis(2,4-pentanedionato) palladium(II)",Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19169,T3D1585,"Diamminedichloro-palladium(II), cis",Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19170,T3D1585,"Diamminedichloro-palladium(II), cis",Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19171,T3D1585,"Diamminedichloro-palladium(II), cis",Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19172,T3D1585,"Diamminedichloro-palladium(II), cis",Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19173,T3D1585,"Diamminedichloro-palladium(II), cis",Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19174,T3D1586,"Diamminedichloro-palladium(II), trans-",Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19175,T3D1586,"Diamminedichloro-palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19176,T3D1586,"Diamminedichloro-palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19177,T3D1586,"Diamminedichloro-palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19178,T3D1586,"Diamminedichloro-palladium(II), trans-",Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19179,T3D1587,"Dichlorobis-(triphenylphosphine) palladium(II), trans-",Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19180,T3D1587,"Dichlorobis-(triphenylphosphine) palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19181,T3D1587,"Dichlorobis-(triphenylphosphine) palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19182,T3D1587,"Dichlorobis-(triphenylphosphine) palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19183,T3D1587,"Dichlorobis-(triphenylphosphine) palladium(II), trans-",Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19184,T3D1588,"Diamminedinitro-palladium(II), trans-",Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19185,T3D1588,"Diamminedinitro-palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19186,T3D1588,"Diamminedinitro-palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19187,T3D1588,"Diamminedinitro-palladium(II), trans-",Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19188,T3D1588,"Diamminedinitro-palladium(II), trans-",Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19189,T3D1589,"Dichloro(1,5-cyclooctadiene) palladium(II)",Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19190,T3D1589,"Dichloro(1,5-cyclooctadiene) palladium(II)",Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19191,T3D1589,"Dichloro(1,5-cyclooctadiene) palladium(II)",Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19192,T3D1589,"Dichloro(1,5-cyclooctadiene) palladium(II)",Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19193,T3D1589,"Dichloro(1,5-cyclooctadiene) palladium(II)",Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19194,T3D1590,Hydrogen tetrachloro-palladate(II),Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19195,T3D1590,Hydrogen tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19196,T3D1590,Hydrogen tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19197,T3D1590,Hydrogen tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19198,T3D1590,Hydrogen tetrachloro-palladate(II),Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19199,T3D1591,Palladium(II) iodide,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19200,T3D1591,Palladium(II) iodide,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19201,T3D1591,Palladium(II) iodide,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19202,T3D1591,Palladium(II) iodide,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19203,T3D1591,Palladium(II) iodide,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19204,T3D1592,Palladium(II) sulfate,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19205,T3D1592,Palladium(II) sulfate,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19206,T3D1592,Palladium(II) sulfate,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19207,T3D1592,Palladium(II) sulfate,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19208,T3D1592,Palladium(II) sulfate,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19209,T3D1593,Potassium hexachloro-palladate(IV),Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19210,T3D1593,Potassium hexachloro-palladate(IV),Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19211,T3D1593,Potassium hexachloro-palladate(IV),Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19212,T3D1593,Potassium hexachloro-palladate(IV),Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19213,T3D1593,Potassium hexachloro-palladate(IV),Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19214,T3D1594,Sodium tetrachloro-palladate(II),Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19215,T3D1594,Sodium tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19216,T3D1594,Sodium tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19217,T3D1594,Sodium tetrachloro-palladate(II),Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19218,T3D1594,Sodium tetrachloro-palladate(II),Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19219,T3D1595,Tetraammine palladium(II) chloride,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19220,T3D1595,Tetraammine palladium(II) chloride,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19221,T3D1595,Tetraammine palladium(II) chloride,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19222,T3D1595,Tetraammine palladium(II) chloride,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19223,T3D1595,Tetraammine palladium(II) chloride,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19224,T3D1596,Tetraammine palladium hydrogen carbonate,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19225,T3D1596,Tetraammine palladium hydrogen carbonate,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19226,T3D1596,Tetraammine palladium hydrogen carbonate,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19227,T3D1596,Tetraammine palladium hydrogen carbonate,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19228,T3D1596,Tetraammine palladium hydrogen carbonate,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19229,T3D1648,Palladium(II) cyanide,Creatine kinase M-type,P06732,Palladium inhibits creatine kinase by forming a complex with its essential SH groups. (S066)
19230,T3D1648,Palladium(II) cyanide,Prolyl 4-hydroxylase subunit alpha-1,P13674,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19231,T3D1648,Palladium(II) cyanide,Prolyl 4-hydroxylase subunit alpha-2,O15460,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19232,T3D1648,Palladium(II) cyanide,Prolyl 4-hydroxylase subunit alpha-3,Q7Z4N8,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19233,T3D1648,Palladium(II) cyanide,Putative HIF-prolyl hydroxylase PH-4,Q9NXG6,"Palladium irreversibly inhibits prolyl hydroxylase by replacing Fe2+ in the active site, forming a strong complex with the enzyme. (S067)"
19234,T3D1598,Argyrol,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19235,T3D1598,Argyrol,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19236,T3D1598,Argyrol,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19237,T3D1598,Argyrol,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19238,T3D1598,Argyrol,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19239,T3D1598,Argyrol,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19240,T3D1598,Argyrol,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19241,T3D1598,Argyrol,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19242,T3D1598,Argyrol,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19243,T3D1598,Argyrol,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19244,T3D1598,Argyrol,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19245,T3D1598,Argyrol,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19246,T3D1598,Argyrol,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19247,T3D1598,Argyrol,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19248,T3D1598,Argyrol,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19249,T3D1598,Argyrol,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19250,T3D1599,Silver acetate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19251,T3D1599,Silver acetate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19252,T3D1599,Silver acetate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19253,T3D1599,Silver acetate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19254,T3D1599,Silver acetate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19255,T3D1599,Silver acetate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19256,T3D1599,Silver acetate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19257,T3D1599,Silver acetate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19258,T3D1599,Silver acetate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19259,T3D1599,Silver acetate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19260,T3D1599,Silver acetate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19261,T3D1599,Silver acetate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19262,T3D1599,Silver acetate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19263,T3D1599,Silver acetate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19264,T3D1599,Silver acetate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19265,T3D1599,Silver acetate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19266,T3D1600,Silver acetylide,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19267,T3D1600,Silver acetylide,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19268,T3D1600,Silver acetylide,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19269,T3D1600,Silver acetylide,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19270,T3D1600,Silver acetylide,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19271,T3D1600,Silver acetylide,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19272,T3D1600,Silver acetylide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19273,T3D1600,Silver acetylide,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19274,T3D1600,Silver acetylide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19275,T3D1600,Silver acetylide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19276,T3D1600,Silver acetylide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19277,T3D1600,Silver acetylide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19278,T3D1600,Silver acetylide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19279,T3D1600,Silver acetylide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19280,T3D1600,Silver acetylide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19281,T3D1600,Silver acetylide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19282,T3D1601,Silver azide,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19283,T3D1601,Silver azide,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19284,T3D1601,Silver azide,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19285,T3D1601,Silver azide,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19286,T3D1601,Silver azide,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19287,T3D1601,Silver azide,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19288,T3D1601,Silver azide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19289,T3D1601,Silver azide,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19290,T3D1601,Silver azide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19291,T3D1601,Silver azide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19292,T3D1601,Silver azide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19293,T3D1601,Silver azide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19294,T3D1601,Silver azide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19295,T3D1601,Silver azide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19296,T3D1601,Silver azide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19297,T3D1601,Silver azide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19298,T3D1602,Silver carbonate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19299,T3D1602,Silver carbonate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19300,T3D1602,Silver carbonate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19301,T3D1602,Silver carbonate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19302,T3D1602,Silver carbonate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19303,T3D1602,Silver carbonate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19304,T3D1602,Silver carbonate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19305,T3D1602,Silver carbonate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19306,T3D1602,Silver carbonate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19307,T3D1602,Silver carbonate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19308,T3D1602,Silver carbonate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19309,T3D1602,Silver carbonate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19310,T3D1602,Silver carbonate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19311,T3D1602,Silver carbonate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19312,T3D1602,Silver carbonate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19313,T3D1602,Silver carbonate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19314,T3D1603,Silver chlorate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19315,T3D1603,Silver chlorate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19316,T3D1603,Silver chlorate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19317,T3D1603,Silver chlorate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19318,T3D1603,Silver chlorate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19319,T3D1603,Silver chlorate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19320,T3D1603,Silver chlorate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19321,T3D1603,Silver chlorate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19322,T3D1603,Silver chlorate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19323,T3D1603,Silver chlorate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19324,T3D1603,Silver chlorate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19325,T3D1603,Silver chlorate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19326,T3D1603,Silver chlorate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19327,T3D1603,Silver chlorate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19328,T3D1603,Silver chlorate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19329,T3D1603,Silver chlorate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19330,T3D1604,Silver chloride,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19331,T3D1604,Silver chloride,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19332,T3D1604,Silver chloride,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19333,T3D1604,Silver chloride,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19334,T3D1604,Silver chloride,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19335,T3D1604,Silver chloride,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19336,T3D1604,Silver chloride,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19337,T3D1604,Silver chloride,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19338,T3D1604,Silver chloride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19339,T3D1604,Silver chloride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19340,T3D1604,Silver chloride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19341,T3D1604,Silver chloride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19342,T3D1604,Silver chloride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19343,T3D1604,Silver chloride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19344,T3D1604,Silver chloride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19345,T3D1604,Silver chloride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19346,T3D1605,Silver fulminate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19347,T3D1605,Silver fulminate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19348,T3D1605,Silver fulminate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19349,T3D1605,Silver fulminate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19350,T3D1605,Silver fulminate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19351,T3D1605,Silver fulminate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19352,T3D1605,Silver fulminate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19353,T3D1605,Silver fulminate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19354,T3D1605,Silver fulminate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19355,T3D1605,Silver fulminate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19356,T3D1605,Silver fulminate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19357,T3D1605,Silver fulminate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19358,T3D1605,Silver fulminate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19359,T3D1605,Silver fulminate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19360,T3D1605,Silver fulminate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19361,T3D1605,Silver fulminate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19362,T3D1606,Silver hexafluorophosphate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19363,T3D1606,Silver hexafluorophosphate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19364,T3D1606,Silver hexafluorophosphate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19365,T3D1606,Silver hexafluorophosphate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19366,T3D1606,Silver hexafluorophosphate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19367,T3D1606,Silver hexafluorophosphate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19368,T3D1606,Silver hexafluorophosphate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19369,T3D1606,Silver hexafluorophosphate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19370,T3D1606,Silver hexafluorophosphate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19371,T3D1606,Silver hexafluorophosphate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19372,T3D1606,Silver hexafluorophosphate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19373,T3D1606,Silver hexafluorophosphate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19374,T3D1606,Silver hexafluorophosphate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19375,T3D1606,Silver hexafluorophosphate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19376,T3D1606,Silver hexafluorophosphate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19377,T3D1606,Silver hexafluorophosphate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19378,T3D1607,Silver iodate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19379,T3D1607,Silver iodate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19380,T3D1607,Silver iodate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19381,T3D1607,Silver iodate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19382,T3D1607,Silver iodate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19383,T3D1607,Silver iodate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19384,T3D1607,Silver iodate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19385,T3D1607,Silver iodate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19386,T3D1607,Silver iodate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19387,T3D1607,Silver iodate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19388,T3D1607,Silver iodate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19389,T3D1607,Silver iodate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19390,T3D1607,Silver iodate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19391,T3D1607,Silver iodate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19392,T3D1607,Silver iodate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19393,T3D1607,Silver iodate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19394,T3D1608,Silver iodide,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19395,T3D1608,Silver iodide,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19396,T3D1608,Silver iodide,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19397,T3D1608,Silver iodide,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19398,T3D1608,Silver iodide,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19399,T3D1608,Silver iodide,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19400,T3D1608,Silver iodide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19401,T3D1608,Silver iodide,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19402,T3D1608,Silver iodide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19403,T3D1608,Silver iodide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19404,T3D1608,Silver iodide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19405,T3D1608,Silver iodide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19406,T3D1608,Silver iodide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19407,T3D1608,Silver iodide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19408,T3D1608,Silver iodide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19409,T3D1608,Silver iodide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19410,T3D1609,Silver molybdate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19411,T3D1609,Silver molybdate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19412,T3D1609,Silver molybdate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19413,T3D1609,Silver molybdate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19414,T3D1609,Silver molybdate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19415,T3D1609,Silver molybdate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19416,T3D1609,Silver molybdate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19417,T3D1609,Silver molybdate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19418,T3D1609,Silver molybdate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19419,T3D1609,Silver molybdate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19420,T3D1609,Silver molybdate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19421,T3D1609,Silver molybdate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19422,T3D1609,Silver molybdate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19423,T3D1609,Silver molybdate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19424,T3D1609,Silver molybdate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19425,T3D1609,Silver molybdate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19426,T3D1610,Silver nitrate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19427,T3D1610,Silver nitrate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19428,T3D1610,Silver nitrate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19429,T3D1610,Silver nitrate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19430,T3D1610,Silver nitrate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19431,T3D1610,Silver nitrate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19432,T3D1610,Silver nitrate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19433,T3D1610,Silver nitrate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19434,T3D1610,Silver nitrate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19435,T3D1610,Silver nitrate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19436,T3D1610,Silver nitrate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19437,T3D1610,Silver nitrate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19438,T3D1610,Silver nitrate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19439,T3D1610,Silver nitrate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19440,T3D1610,Silver nitrate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19441,T3D1610,Silver nitrate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19442,T3D1611,Silver oxalate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19443,T3D1611,Silver oxalate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19444,T3D1611,Silver oxalate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19445,T3D1611,Silver oxalate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19446,T3D1611,Silver oxalate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19447,T3D1611,Silver oxalate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19448,T3D1611,Silver oxalate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19449,T3D1611,Silver oxalate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19450,T3D1611,Silver oxalate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19451,T3D1611,Silver oxalate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19452,T3D1611,Silver oxalate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19453,T3D1611,Silver oxalate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19454,T3D1611,Silver oxalate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19455,T3D1611,Silver oxalate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19456,T3D1611,Silver oxalate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19457,T3D1611,Silver oxalate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19458,T3D1612,Silver oxide,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19459,T3D1612,Silver oxide,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19460,T3D1612,Silver oxide,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19461,T3D1612,Silver oxide,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19462,T3D1612,Silver oxide,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19463,T3D1612,Silver oxide,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19464,T3D1612,Silver oxide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19465,T3D1612,Silver oxide,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19466,T3D1612,Silver oxide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19467,T3D1612,Silver oxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19468,T3D1612,Silver oxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19469,T3D1612,Silver oxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19470,T3D1612,Silver oxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19471,T3D1612,Silver oxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19472,T3D1612,Silver oxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19473,T3D1612,Silver oxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19474,T3D1613,Silver perchlorate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19475,T3D1613,Silver perchlorate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19476,T3D1613,Silver perchlorate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19477,T3D1613,Silver perchlorate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19478,T3D1613,Silver perchlorate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19479,T3D1613,Silver perchlorate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19480,T3D1613,Silver perchlorate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19481,T3D1613,Silver perchlorate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19482,T3D1613,Silver perchlorate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19483,T3D1613,Silver perchlorate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19484,T3D1613,Silver perchlorate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19485,T3D1613,Silver perchlorate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19486,T3D1613,Silver perchlorate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19487,T3D1613,Silver perchlorate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19488,T3D1613,Silver perchlorate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19489,T3D1613,Silver perchlorate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19490,T3D1614,Silver perchlorate monohydrate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19491,T3D1614,Silver perchlorate monohydrate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19492,T3D1614,Silver perchlorate monohydrate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19493,T3D1614,Silver perchlorate monohydrate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19494,T3D1614,Silver perchlorate monohydrate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19495,T3D1614,Silver perchlorate monohydrate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19496,T3D1614,Silver perchlorate monohydrate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19497,T3D1614,Silver perchlorate monohydrate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19498,T3D1614,Silver perchlorate monohydrate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19499,T3D1614,Silver perchlorate monohydrate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19500,T3D1614,Silver perchlorate monohydrate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19501,T3D1614,Silver perchlorate monohydrate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19502,T3D1614,Silver perchlorate monohydrate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19503,T3D1614,Silver perchlorate monohydrate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19504,T3D1614,Silver perchlorate monohydrate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19505,T3D1614,Silver perchlorate monohydrate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19506,T3D1615,Silver subfluoride,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19507,T3D1615,Silver subfluoride,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19508,T3D1615,Silver subfluoride,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19509,T3D1615,Silver subfluoride,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19510,T3D1615,Silver subfluoride,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19511,T3D1615,Silver subfluoride,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19512,T3D1615,Silver subfluoride,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19513,T3D1615,Silver subfluoride,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19514,T3D1615,Silver subfluoride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19515,T3D1615,Silver subfluoride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19516,T3D1615,Silver subfluoride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19517,T3D1615,Silver subfluoride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19518,T3D1615,Silver subfluoride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19519,T3D1615,Silver subfluoride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19520,T3D1615,Silver subfluoride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19521,T3D1615,Silver subfluoride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19522,T3D1616,Silver sulfate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19523,T3D1616,Silver sulfate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19524,T3D1616,Silver sulfate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19525,T3D1616,Silver sulfate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19526,T3D1616,Silver sulfate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19527,T3D1616,Silver sulfate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19528,T3D1616,Silver sulfate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19529,T3D1616,Silver sulfate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19530,T3D1616,Silver sulfate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19531,T3D1616,Silver sulfate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19532,T3D1616,Silver sulfate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19533,T3D1616,Silver sulfate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19534,T3D1616,Silver sulfate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19535,T3D1616,Silver sulfate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19536,T3D1616,Silver sulfate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19537,T3D1616,Silver sulfate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19538,T3D1617,Silver sulfide,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19539,T3D1617,Silver sulfide,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19540,T3D1617,Silver sulfide,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19541,T3D1617,Silver sulfide,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19542,T3D1617,Silver sulfide,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19543,T3D1617,Silver sulfide,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19544,T3D1617,Silver sulfide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19545,T3D1617,Silver sulfide,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19546,T3D1617,Silver sulfide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19547,T3D1617,Silver sulfide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19548,T3D1617,Silver sulfide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19549,T3D1617,Silver sulfide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19550,T3D1617,Silver sulfide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19551,T3D1617,Silver sulfide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19552,T3D1617,Silver sulfide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19553,T3D1617,Silver sulfide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19554,T3D1618,Silver telluride,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19555,T3D1618,Silver telluride,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19556,T3D1618,Silver telluride,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19557,T3D1618,Silver telluride,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19558,T3D1618,Silver telluride,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19559,T3D1618,Silver telluride,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19560,T3D1618,Silver telluride,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19561,T3D1618,Silver telluride,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19562,T3D1618,Silver telluride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19563,T3D1618,Silver telluride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19564,T3D1618,Silver telluride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19565,T3D1618,Silver telluride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19566,T3D1618,Silver telluride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19567,T3D1618,Silver telluride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19568,T3D1618,Silver telluride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19569,T3D1618,Silver telluride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19570,T3D1619,Silver tetrafluoroborate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19571,T3D1619,Silver tetrafluoroborate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19572,T3D1619,Silver tetrafluoroborate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19573,T3D1619,Silver tetrafluoroborate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19574,T3D1619,Silver tetrafluoroborate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19575,T3D1619,Silver tetrafluoroborate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19576,T3D1619,Silver tetrafluoroborate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19577,T3D1619,Silver tetrafluoroborate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19578,T3D1619,Silver tetrafluoroborate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19579,T3D1619,Silver tetrafluoroborate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19580,T3D1619,Silver tetrafluoroborate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19581,T3D1619,Silver tetrafluoroborate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19582,T3D1619,Silver tetrafluoroborate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19583,T3D1619,Silver tetrafluoroborate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19584,T3D1619,Silver tetrafluoroborate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19585,T3D1619,Silver tetrafluoroborate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19586,T3D1620,Silver trifluoromethanesulfonate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19587,T3D1620,Silver trifluoromethanesulfonate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19588,T3D1620,Silver trifluoromethanesulfonate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19589,T3D1620,Silver trifluoromethanesulfonate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19590,T3D1620,Silver trifluoromethanesulfonate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19591,T3D1620,Silver trifluoromethanesulfonate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19592,T3D1620,Silver trifluoromethanesulfonate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19593,T3D1620,Silver trifluoromethanesulfonate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19594,T3D1620,Silver trifluoromethanesulfonate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19595,T3D1620,Silver trifluoromethanesulfonate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19596,T3D1620,Silver trifluoromethanesulfonate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19597,T3D1620,Silver trifluoromethanesulfonate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19598,T3D1620,Silver trifluoromethanesulfonate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19599,T3D1620,Silver trifluoromethanesulfonate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19600,T3D1620,Silver trifluoromethanesulfonate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19601,T3D1620,Silver trifluoromethanesulfonate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19602,T3D1621,Silver(II) fluoride,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19603,T3D1621,Silver(II) fluoride,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19604,T3D1621,Silver(II) fluoride,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19605,T3D1621,Silver(II) fluoride,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19606,T3D1621,Silver(II) fluoride,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19607,T3D1621,Silver(II) fluoride,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19608,T3D1621,Silver(II) fluoride,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19609,T3D1621,Silver(II) fluoride,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19610,T3D1621,Silver(II) fluoride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19611,T3D1621,Silver(II) fluoride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19612,T3D1621,Silver(II) fluoride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19613,T3D1621,Silver(II) fluoride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19614,T3D1621,Silver(II) fluoride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19615,T3D1621,Silver(II) fluoride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19616,T3D1621,Silver(II) fluoride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19617,T3D1621,Silver(II) fluoride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19618,T3D1622,"Silver(I,III) oxide",Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19619,T3D1622,"Silver(I,III) oxide",Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19620,T3D1622,"Silver(I,III) oxide",Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19621,T3D1622,"Silver(I,III) oxide",Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19622,T3D1622,"Silver(I,III) oxide",Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19623,T3D1622,"Silver(I,III) oxide",Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19624,T3D1622,"Silver(I,III) oxide","Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19625,T3D1622,"Silver(I,III) oxide",Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19626,T3D1622,"Silver(I,III) oxide",Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19627,T3D1622,"Silver(I,III) oxide",Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19628,T3D1622,"Silver(I,III) oxide",Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19629,T3D1622,"Silver(I,III) oxide",Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19630,T3D1622,"Silver(I,III) oxide",Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19631,T3D1622,"Silver(I,III) oxide",Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19632,T3D1622,"Silver(I,III) oxide",Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19633,T3D1622,"Silver(I,III) oxide",Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19634,T3D1717,Silver bromate,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19635,T3D1717,Silver bromate,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19636,T3D1717,Silver bromate,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19637,T3D1717,Silver bromate,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19638,T3D1717,Silver bromate,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19639,T3D1717,Silver bromate,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19640,T3D1717,Silver bromate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19641,T3D1717,Silver bromate,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19642,T3D1717,Silver bromate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19643,T3D1717,Silver bromate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19644,T3D1717,Silver bromate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19645,T3D1717,Silver bromate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19646,T3D1717,Silver bromate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19647,T3D1717,Silver bromate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19648,T3D1717,Silver bromate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19649,T3D1717,Silver bromate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19650,T3D1753,Silver bromide,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19651,T3D1753,Silver bromide,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19652,T3D1753,Silver bromide,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19653,T3D1753,Silver bromide,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19654,T3D1753,Silver bromide,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19655,T3D1753,Silver bromide,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19656,T3D1753,Silver bromide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19657,T3D1753,Silver bromide,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19658,T3D1753,Silver bromide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19659,T3D1753,Silver bromide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19660,T3D1753,Silver bromide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19661,T3D1753,Silver bromide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19662,T3D1753,Silver bromide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19663,T3D1753,Silver bromide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19664,T3D1753,Silver bromide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19665,T3D1753,Silver bromide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19666,T3D1836,Silver(I) selenide,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19667,T3D1836,Silver(I) selenide,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19668,T3D1836,Silver(I) selenide,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19669,T3D1836,Silver(I) selenide,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19670,T3D1836,Silver(I) selenide,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19671,T3D1836,Silver(I) selenide,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19672,T3D1836,Silver(I) selenide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19673,T3D1836,Silver(I) selenide,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19674,T3D1836,Silver(I) selenide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19675,T3D1836,Silver(I) selenide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19676,T3D1836,Silver(I) selenide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19677,T3D1836,Silver(I) selenide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19678,T3D1836,Silver(I) selenide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19679,T3D1836,Silver(I) selenide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19680,T3D1836,Silver(I) selenide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19681,T3D1836,Silver(I) selenide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19682,T3D1838,Silver selenite,Epididymal secretory glutathione peroxidase,O75715,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19683,T3D1838,Silver selenite,Glutathione peroxidase 1,P07203,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19684,T3D1838,Silver selenite,Glutathione peroxidase 2,P18283,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19685,T3D1838,Silver selenite,Glutathione peroxidase 3,P22352,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19686,T3D1838,Silver selenite,Glutathione peroxidase 6,P59796,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19687,T3D1838,Silver selenite,Glutathione peroxidase 7,Q96SL4,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19688,T3D1838,Silver selenite,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19689,T3D1838,Silver selenite,Probable glutathione peroxidase 8,Q8TED1 ,"The silver ion is known to inhibit glutathione peroxidase activity, disrupting selenium-catalyzed sulfhydryl oxidation-reduction reactions. (S080)"
19690,T3D1838,Silver selenite,Sodium/potassium-transporting ATPase gamma chain,P54710,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19691,T3D1838,Silver selenite,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19692,T3D1838,Silver selenite,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19693,T3D1838,Silver selenite,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19694,T3D1838,Silver selenite,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19695,T3D1838,Silver selenite,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19696,T3D1838,Silver selenite,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19697,T3D1838,Silver selenite,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The silver ion is known to inhibit NA+,K+-ATPase activity, disrupting intracellular ion concentrations. (S077)"
19698,T3D1624,Vanadium carbide,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19699,T3D1624,Vanadium carbide,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19700,T3D1624,Vanadium carbide,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19701,T3D1624,Vanadium carbide,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19702,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19703,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19704,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19705,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19706,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19707,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19708,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19709,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19710,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19711,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19712,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19713,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19714,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19715,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19716,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19717,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19718,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19719,T3D1624,Vanadium carbide,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19720,T3D1624,Vanadium carbide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19721,T3D1624,Vanadium carbide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19722,T3D1624,Vanadium carbide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19723,T3D1624,Vanadium carbide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19724,T3D1624,Vanadium carbide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19725,T3D1624,Vanadium carbide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19726,T3D1624,Vanadium carbide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19727,T3D1624,Vanadium carbide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19728,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19729,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19730,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19731,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19732,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19733,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19734,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19735,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19736,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19737,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19738,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19739,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19740,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19741,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19742,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19743,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19744,T3D1624,Vanadium carbide,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19745,T3D1625,Vanadium carbonyl,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19746,T3D1625,Vanadium carbonyl,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19747,T3D1625,Vanadium carbonyl,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19748,T3D1625,Vanadium carbonyl,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19749,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19750,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19751,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19752,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19753,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19754,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19755,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19756,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19757,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19758,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19759,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19760,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19761,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19762,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19763,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19764,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19765,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19766,T3D1625,Vanadium carbonyl,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19767,T3D1625,Vanadium carbonyl,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19768,T3D1625,Vanadium carbonyl,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19769,T3D1625,Vanadium carbonyl,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19770,T3D1625,Vanadium carbonyl,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19771,T3D1625,Vanadium carbonyl,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19772,T3D1625,Vanadium carbonyl,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19773,T3D1625,Vanadium carbonyl,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19774,T3D1625,Vanadium carbonyl,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19775,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19776,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19777,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19778,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19779,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19780,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19781,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19782,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19783,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19784,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19785,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19786,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19787,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19788,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19789,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19790,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19791,T3D1625,Vanadium carbonyl,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19792,T3D1626,Vanadium nitride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19793,T3D1626,Vanadium nitride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19794,T3D1626,Vanadium nitride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19795,T3D1626,Vanadium nitride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19796,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19797,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19798,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19799,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19800,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19801,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19802,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19803,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19804,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19805,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19806,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19807,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19808,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19809,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19810,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19811,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19812,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19813,T3D1626,Vanadium nitride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19814,T3D1626,Vanadium nitride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19815,T3D1626,Vanadium nitride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19816,T3D1626,Vanadium nitride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19817,T3D1626,Vanadium nitride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19818,T3D1626,Vanadium nitride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19819,T3D1626,Vanadium nitride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19820,T3D1626,Vanadium nitride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19821,T3D1626,Vanadium nitride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19822,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19823,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19824,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19825,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19826,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19827,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19828,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19829,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19830,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19831,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19832,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19833,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19834,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19835,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19836,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19837,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19838,T3D1626,Vanadium nitride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19839,T3D1627,Vanadium oxytrichloride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19840,T3D1627,Vanadium oxytrichloride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19841,T3D1627,Vanadium oxytrichloride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19842,T3D1627,Vanadium oxytrichloride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19843,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19844,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19845,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19846,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19847,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19848,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19849,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19850,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19851,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19852,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19853,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19854,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19855,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19856,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19857,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19858,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19859,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19860,T3D1627,Vanadium oxytrichloride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19861,T3D1627,Vanadium oxytrichloride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19862,T3D1627,Vanadium oxytrichloride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19863,T3D1627,Vanadium oxytrichloride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19864,T3D1627,Vanadium oxytrichloride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19865,T3D1627,Vanadium oxytrichloride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19866,T3D1627,Vanadium oxytrichloride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19867,T3D1627,Vanadium oxytrichloride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19868,T3D1627,Vanadium oxytrichloride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19869,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19870,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19871,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19872,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19873,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19874,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19875,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19876,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19877,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19878,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19879,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19880,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19881,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19882,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19883,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19884,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19885,T3D1627,Vanadium oxytrichloride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19886,T3D1628,Vanadium tetrachloride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19887,T3D1628,Vanadium tetrachloride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19888,T3D1628,Vanadium tetrachloride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19889,T3D1628,Vanadium tetrachloride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19890,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19891,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19892,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19893,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19894,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19895,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19896,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19897,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19898,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19899,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19900,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19901,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19902,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19903,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19904,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19905,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19906,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19907,T3D1628,Vanadium tetrachloride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19908,T3D1628,Vanadium tetrachloride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19909,T3D1628,Vanadium tetrachloride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19910,T3D1628,Vanadium tetrachloride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19911,T3D1628,Vanadium tetrachloride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19912,T3D1628,Vanadium tetrachloride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19913,T3D1628,Vanadium tetrachloride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19914,T3D1628,Vanadium tetrachloride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19915,T3D1628,Vanadium tetrachloride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19916,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19917,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19918,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19919,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19920,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19921,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19922,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19923,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19924,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19925,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19926,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19927,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19928,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19929,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19930,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19931,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19932,T3D1628,Vanadium tetrachloride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19933,T3D1629,Vanadium(II) chloride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19934,T3D1629,Vanadium(II) chloride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19935,T3D1629,Vanadium(II) chloride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19936,T3D1629,Vanadium(II) chloride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19937,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19938,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19939,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19940,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19941,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19942,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19943,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19944,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19945,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19946,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19947,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19948,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19949,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19950,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19951,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19952,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19953,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19954,T3D1629,Vanadium(II) chloride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19955,T3D1629,Vanadium(II) chloride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19956,T3D1629,Vanadium(II) chloride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19957,T3D1629,Vanadium(II) chloride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19958,T3D1629,Vanadium(II) chloride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19959,T3D1629,Vanadium(II) chloride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19960,T3D1629,Vanadium(II) chloride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19961,T3D1629,Vanadium(II) chloride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19962,T3D1629,Vanadium(II) chloride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
19963,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19964,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19965,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19966,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19967,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19968,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19969,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19970,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19971,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19972,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19973,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19974,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19975,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19976,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19977,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19978,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19979,T3D1629,Vanadium(II) chloride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19980,T3D1630,Vanadium(II) oxide,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19981,T3D1630,Vanadium(II) oxide,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19982,T3D1630,Vanadium(II) oxide,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19983,T3D1630,Vanadium(II) oxide,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19984,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19985,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19986,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19987,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19988,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19989,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19990,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19991,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19992,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19993,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19994,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19995,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19996,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19997,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19998,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
19999,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20000,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20001,T3D1630,Vanadium(II) oxide,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20002,T3D1630,Vanadium(II) oxide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20003,T3D1630,Vanadium(II) oxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20004,T3D1630,Vanadium(II) oxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20005,T3D1630,Vanadium(II) oxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20006,T3D1630,Vanadium(II) oxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20007,T3D1630,Vanadium(II) oxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20008,T3D1630,Vanadium(II) oxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20009,T3D1630,Vanadium(II) oxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20010,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20011,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20012,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20013,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20014,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20015,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20016,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20017,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20018,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20019,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20020,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20021,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20022,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20023,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20024,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20025,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20026,T3D1630,Vanadium(II) oxide,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20027,T3D1631,Vanadium(III) chloride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20028,T3D1631,Vanadium(III) chloride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20029,T3D1631,Vanadium(III) chloride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20030,T3D1631,Vanadium(III) chloride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20031,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20032,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20033,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20034,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20035,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20036,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20037,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20038,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20039,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20040,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20041,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20042,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20043,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20044,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20045,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20046,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20047,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20048,T3D1631,Vanadium(III) chloride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20049,T3D1631,Vanadium(III) chloride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20050,T3D1631,Vanadium(III) chloride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20051,T3D1631,Vanadium(III) chloride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20052,T3D1631,Vanadium(III) chloride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20053,T3D1631,Vanadium(III) chloride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20054,T3D1631,Vanadium(III) chloride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20055,T3D1631,Vanadium(III) chloride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20056,T3D1631,Vanadium(III) chloride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20057,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20058,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20059,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20060,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20061,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20062,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20063,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20064,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20065,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20066,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20067,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20068,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20069,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20070,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20071,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20072,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20073,T3D1631,Vanadium(III) chloride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20074,T3D1632,Vanadium(III) fluoride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20075,T3D1632,Vanadium(III) fluoride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20076,T3D1632,Vanadium(III) fluoride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20077,T3D1632,Vanadium(III) fluoride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20078,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20079,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20080,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20081,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20082,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20083,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20084,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20085,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20086,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20087,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20088,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20089,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20090,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20091,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20092,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20093,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20094,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20095,T3D1632,Vanadium(III) fluoride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20096,T3D1632,Vanadium(III) fluoride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20097,T3D1632,Vanadium(III) fluoride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20098,T3D1632,Vanadium(III) fluoride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20099,T3D1632,Vanadium(III) fluoride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20100,T3D1632,Vanadium(III) fluoride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20101,T3D1632,Vanadium(III) fluoride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20102,T3D1632,Vanadium(III) fluoride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20103,T3D1632,Vanadium(III) fluoride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20104,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20105,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20106,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20107,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20108,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20109,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20110,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20111,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20112,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20113,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20114,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20115,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20116,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20117,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20118,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20119,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20120,T3D1632,Vanadium(III) fluoride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20121,T3D1633,Vanadium(III) iodide,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20122,T3D1633,Vanadium(III) iodide,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20123,T3D1633,Vanadium(III) iodide,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20124,T3D1633,Vanadium(III) iodide,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20125,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20126,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20127,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20128,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20129,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20130,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20131,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20132,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20133,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20134,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20135,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20136,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20137,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20138,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20139,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20140,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20141,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20142,T3D1633,Vanadium(III) iodide,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20143,T3D1633,Vanadium(III) iodide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20144,T3D1633,Vanadium(III) iodide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20145,T3D1633,Vanadium(III) iodide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20146,T3D1633,Vanadium(III) iodide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20147,T3D1633,Vanadium(III) iodide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20148,T3D1633,Vanadium(III) iodide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20149,T3D1633,Vanadium(III) iodide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20150,T3D1633,Vanadium(III) iodide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20151,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20152,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20153,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20154,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20155,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20156,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20157,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20158,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20159,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20160,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20161,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20162,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20163,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20164,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20165,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20166,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20167,T3D1633,Vanadium(III) iodide,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20168,T3D1634,Vanadium(III) oxide,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20169,T3D1634,Vanadium(III) oxide,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20170,T3D1634,Vanadium(III) oxide,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20171,T3D1634,Vanadium(III) oxide,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20172,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20173,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20174,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20175,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20176,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20177,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20178,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20179,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20180,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20181,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20182,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20183,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20184,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20185,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20186,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20187,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20188,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20189,T3D1634,Vanadium(III) oxide,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20190,T3D1634,Vanadium(III) oxide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20191,T3D1634,Vanadium(III) oxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20192,T3D1634,Vanadium(III) oxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20193,T3D1634,Vanadium(III) oxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20194,T3D1634,Vanadium(III) oxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20195,T3D1634,Vanadium(III) oxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20196,T3D1634,Vanadium(III) oxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20197,T3D1634,Vanadium(III) oxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20198,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20199,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20200,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20201,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20202,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20203,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20204,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20205,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20206,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20207,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20208,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20209,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20210,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20211,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20212,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20213,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20214,T3D1634,Vanadium(III) oxide,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20215,T3D1635,Vanadium(III) sulfate,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20216,T3D1635,Vanadium(III) sulfate,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20217,T3D1635,Vanadium(III) sulfate,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20218,T3D1635,Vanadium(III) sulfate,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20219,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20220,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20221,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20222,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20223,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20224,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20225,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20226,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20227,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20228,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20229,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20230,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20231,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20232,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20233,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20234,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20235,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20236,T3D1635,Vanadium(III) sulfate,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20237,T3D1635,Vanadium(III) sulfate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20238,T3D1635,Vanadium(III) sulfate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20239,T3D1635,Vanadium(III) sulfate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20240,T3D1635,Vanadium(III) sulfate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20241,T3D1635,Vanadium(III) sulfate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20242,T3D1635,Vanadium(III) sulfate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20243,T3D1635,Vanadium(III) sulfate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20244,T3D1635,Vanadium(III) sulfate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20245,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20246,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20247,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20248,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20249,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20250,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20251,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20252,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20253,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20254,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20255,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20256,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20257,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20258,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20259,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20260,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20261,T3D1635,Vanadium(III) sulfate,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20262,T3D1636,Vanadium(IV) fluoride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20263,T3D1636,Vanadium(IV) fluoride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20264,T3D1636,Vanadium(IV) fluoride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20265,T3D1636,Vanadium(IV) fluoride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20266,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20267,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20268,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20269,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20270,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20271,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20272,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20273,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20274,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20275,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20276,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20277,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20278,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20279,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20280,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20281,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20282,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20283,T3D1636,Vanadium(IV) fluoride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20284,T3D1636,Vanadium(IV) fluoride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20285,T3D1636,Vanadium(IV) fluoride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20286,T3D1636,Vanadium(IV) fluoride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20287,T3D1636,Vanadium(IV) fluoride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20288,T3D1636,Vanadium(IV) fluoride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20289,T3D1636,Vanadium(IV) fluoride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20290,T3D1636,Vanadium(IV) fluoride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20291,T3D1636,Vanadium(IV) fluoride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20292,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20293,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20294,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20295,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20296,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20297,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20298,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20299,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20300,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20301,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20302,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20303,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20304,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20305,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20306,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20307,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20308,T3D1636,Vanadium(IV) fluoride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20309,T3D1637,Vanadyl sulfate,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20310,T3D1637,Vanadyl sulfate,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20311,T3D1637,Vanadyl sulfate,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20312,T3D1637,Vanadyl sulfate,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20313,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20314,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20315,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20316,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20317,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20318,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20319,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20320,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20321,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20322,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20323,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20324,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20325,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20326,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20327,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20328,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20329,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20330,T3D1637,Vanadyl sulfate,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20331,T3D1637,Vanadyl sulfate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20332,T3D1637,Vanadyl sulfate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20333,T3D1637,Vanadyl sulfate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20334,T3D1637,Vanadyl sulfate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20335,T3D1637,Vanadyl sulfate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20336,T3D1637,Vanadyl sulfate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20337,T3D1637,Vanadyl sulfate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20338,T3D1637,Vanadyl sulfate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20339,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20340,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20341,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20342,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20343,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20344,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20345,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20346,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20347,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20348,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20349,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20350,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20351,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20352,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20353,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20354,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20355,T3D1637,Vanadyl sulfate,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20356,T3D1638,Vanadium(IV) oxide,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20357,T3D1638,Vanadium(IV) oxide,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20358,T3D1638,Vanadium(IV) oxide,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20359,T3D1638,Vanadium(IV) oxide,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20360,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20361,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20362,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20363,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20364,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20365,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20366,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20367,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20368,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20369,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20370,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20371,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20372,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20373,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20374,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20375,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20376,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20377,T3D1638,Vanadium(IV) oxide,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20378,T3D1638,Vanadium(IV) oxide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20379,T3D1638,Vanadium(IV) oxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20380,T3D1638,Vanadium(IV) oxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20381,T3D1638,Vanadium(IV) oxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20382,T3D1638,Vanadium(IV) oxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20383,T3D1638,Vanadium(IV) oxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20384,T3D1638,Vanadium(IV) oxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20385,T3D1638,Vanadium(IV) oxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20386,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20387,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20388,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20389,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20390,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20391,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20392,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20393,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20394,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20395,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20396,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20397,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20398,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20399,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20400,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20401,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20402,T3D1638,Vanadium(IV) oxide,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20403,T3D1639,Vanadium(V) oxide,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20404,T3D1639,Vanadium(V) oxide,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20405,T3D1639,Vanadium(V) oxide,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20406,T3D1639,Vanadium(V) oxide,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20407,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20408,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20409,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20410,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20411,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20412,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20413,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20414,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20415,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20416,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20417,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20418,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20419,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20420,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20421,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20422,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20423,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20424,T3D1639,Vanadium(V) oxide,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20425,T3D1639,Vanadium(V) oxide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20426,T3D1639,Vanadium(V) oxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20427,T3D1639,Vanadium(V) oxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20428,T3D1639,Vanadium(V) oxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20429,T3D1639,Vanadium(V) oxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20430,T3D1639,Vanadium(V) oxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20431,T3D1639,Vanadium(V) oxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20432,T3D1639,Vanadium(V) oxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20433,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20434,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20435,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20436,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20437,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20438,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20439,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20440,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20441,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20442,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20443,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20444,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20445,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20446,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20447,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20448,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20449,T3D1639,Vanadium(V) oxide,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20450,T3D1640,Vanadium(V) oxytrifluoride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20451,T3D1640,Vanadium(V) oxytrifluoride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20452,T3D1640,Vanadium(V) oxytrifluoride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20453,T3D1640,Vanadium(V) oxytrifluoride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20454,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20455,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20456,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20457,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20458,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20459,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20460,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20461,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20462,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20463,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20464,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20465,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20466,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20467,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20468,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20469,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20470,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20471,T3D1640,Vanadium(V) oxytrifluoride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20472,T3D1640,Vanadium(V) oxytrifluoride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20473,T3D1640,Vanadium(V) oxytrifluoride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20474,T3D1640,Vanadium(V) oxytrifluoride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20475,T3D1640,Vanadium(V) oxytrifluoride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20476,T3D1640,Vanadium(V) oxytrifluoride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20477,T3D1640,Vanadium(V) oxytrifluoride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20478,T3D1640,Vanadium(V) oxytrifluoride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20479,T3D1640,Vanadium(V) oxytrifluoride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20480,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20481,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20482,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20483,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20484,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20485,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20486,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20487,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20488,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20489,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20490,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20491,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20492,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20493,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20494,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20495,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20496,T3D1640,Vanadium(V) oxytrifluoride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20497,T3D1641,Vanadocene dichloride,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20498,T3D1641,Vanadocene dichloride,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20499,T3D1641,Vanadocene dichloride,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20500,T3D1641,Vanadocene dichloride,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20501,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20502,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20503,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20504,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20505,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20506,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20507,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20508,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20509,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20510,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20511,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20512,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20513,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20514,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20515,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20516,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20517,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20518,T3D1641,Vanadocene dichloride,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20519,T3D1641,Vanadocene dichloride,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20520,T3D1641,Vanadocene dichloride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20521,T3D1641,Vanadocene dichloride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20522,T3D1641,Vanadocene dichloride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20523,T3D1641,Vanadocene dichloride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20524,T3D1641,Vanadocene dichloride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20525,T3D1641,Vanadocene dichloride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20526,T3D1641,Vanadocene dichloride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20527,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20528,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20529,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20530,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20531,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20532,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20533,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20534,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20535,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20536,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20537,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20538,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20539,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20540,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20541,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20542,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20543,T3D1641,Vanadocene dichloride,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20544,T3D1642,Vanadyl acetylacetonate,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20545,T3D1642,Vanadyl acetylacetonate,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20546,T3D1642,Vanadyl acetylacetonate,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20547,T3D1642,Vanadyl acetylacetonate,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20548,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20549,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20550,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20551,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20552,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20553,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20554,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20555,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20556,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20557,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20558,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20559,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20560,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20561,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20562,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20563,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20564,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20565,T3D1642,Vanadyl acetylacetonate,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20566,T3D1642,Vanadyl acetylacetonate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20567,T3D1642,Vanadyl acetylacetonate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20568,T3D1642,Vanadyl acetylacetonate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20569,T3D1642,Vanadyl acetylacetonate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20570,T3D1642,Vanadyl acetylacetonate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20571,T3D1642,Vanadyl acetylacetonate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20572,T3D1642,Vanadyl acetylacetonate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20573,T3D1642,Vanadyl acetylacetonate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20574,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20575,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20576,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20577,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20578,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20579,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20580,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20581,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20582,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20583,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20584,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20585,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20586,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20587,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20588,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20589,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20590,T3D1642,Vanadyl acetylacetonate,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20591,T3D1643,Vanadyl sulfate hydrate,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20592,T3D1643,Vanadyl sulfate hydrate,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20593,T3D1643,Vanadyl sulfate hydrate,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20594,T3D1643,Vanadyl sulfate hydrate,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20595,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20596,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20597,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20598,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20599,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20600,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20601,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20602,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20603,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20604,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20605,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20606,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20607,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20608,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20609,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20610,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20611,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20612,T3D1643,Vanadyl sulfate hydrate,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20613,T3D1643,Vanadyl sulfate hydrate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20614,T3D1643,Vanadyl sulfate hydrate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20615,T3D1643,Vanadyl sulfate hydrate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20616,T3D1643,Vanadyl sulfate hydrate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20617,T3D1643,Vanadyl sulfate hydrate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20618,T3D1643,Vanadyl sulfate hydrate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20619,T3D1643,Vanadyl sulfate hydrate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20620,T3D1643,Vanadyl sulfate hydrate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20621,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20622,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20623,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20624,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20625,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20626,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20627,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20628,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20629,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20630,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20631,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20632,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20633,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20634,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20635,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20636,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20637,T3D1643,Vanadyl sulfate hydrate,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20638,T3D1644,Ammonium vanadate,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20639,T3D1644,Ammonium vanadate,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20640,T3D1644,Ammonium vanadate,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20641,T3D1644,Ammonium vanadate,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20642,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20643,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20644,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20645,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20646,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20647,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20648,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20649,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20650,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20651,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20652,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20653,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20654,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20655,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20656,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20657,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20658,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20659,T3D1644,Ammonium vanadate,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20660,T3D1644,Ammonium vanadate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20661,T3D1644,Ammonium vanadate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20662,T3D1644,Ammonium vanadate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20663,T3D1644,Ammonium vanadate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20664,T3D1644,Ammonium vanadate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20665,T3D1644,Ammonium vanadate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20666,T3D1644,Ammonium vanadate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20667,T3D1644,Ammonium vanadate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20668,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20669,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20670,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20671,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20672,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20673,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20674,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20675,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20676,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20677,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20678,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20679,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20680,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20681,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20682,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20683,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20684,T3D1644,Ammonium vanadate,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20685,T3D1645,Ammonium metavanadate,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20686,T3D1645,Ammonium metavanadate,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20687,T3D1645,Ammonium metavanadate,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20688,T3D1645,Ammonium metavanadate,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20689,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20690,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20691,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20692,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20693,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20694,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20695,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20696,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20697,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20698,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20699,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20700,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20701,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20702,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20703,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20704,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20705,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20706,T3D1645,Ammonium metavanadate,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20707,T3D1645,Ammonium metavanadate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20708,T3D1645,Ammonium metavanadate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20709,T3D1645,Ammonium metavanadate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20710,T3D1645,Ammonium metavanadate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20711,T3D1645,Ammonium metavanadate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20712,T3D1645,Ammonium metavanadate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20713,T3D1645,Ammonium metavanadate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20714,T3D1645,Ammonium metavanadate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20715,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20716,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20717,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20718,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20719,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20720,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20721,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20722,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20723,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20724,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20725,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20726,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20727,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20728,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20729,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20730,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20731,T3D1645,Ammonium metavanadate,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20732,T3D1646,Sodium metavanadate,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20733,T3D1646,Sodium metavanadate,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20734,T3D1646,Sodium metavanadate,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20735,T3D1646,Sodium metavanadate,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20736,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20737,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20738,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20739,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20740,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20741,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20742,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20743,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20744,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20745,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20746,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20747,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20748,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20749,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20750,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20751,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20752,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20753,T3D1646,Sodium metavanadate,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20754,T3D1646,Sodium metavanadate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20755,T3D1646,Sodium metavanadate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20756,T3D1646,Sodium metavanadate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20757,T3D1646,Sodium metavanadate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20758,T3D1646,Sodium metavanadate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20759,T3D1646,Sodium metavanadate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20760,T3D1646,Sodium metavanadate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20761,T3D1646,Sodium metavanadate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20762,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20763,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20764,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20765,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20766,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20767,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20768,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20769,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20770,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20771,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20772,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20773,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20774,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20775,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20776,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20777,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20778,T3D1646,Sodium metavanadate,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20779,T3D1647,Sodium orthovanadate,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20780,T3D1647,Sodium orthovanadate,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20781,T3D1647,Sodium orthovanadate,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20782,T3D1647,Sodium orthovanadate,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20783,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20784,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20785,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20786,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20787,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20788,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20789,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20790,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20791,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20792,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20793,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20794,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20795,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20796,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20797,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20798,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20799,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20800,T3D1647,Sodium orthovanadate,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20801,T3D1647,Sodium orthovanadate,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20802,T3D1647,Sodium orthovanadate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20803,T3D1647,Sodium orthovanadate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20804,T3D1647,Sodium orthovanadate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20805,T3D1647,Sodium orthovanadate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20806,T3D1647,Sodium orthovanadate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20807,T3D1647,Sodium orthovanadate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20808,T3D1647,Sodium orthovanadate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20809,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20810,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20811,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20812,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20813,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20814,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20815,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20816,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20817,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20818,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20819,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20820,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20821,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20822,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20823,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20824,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20825,T3D1647,Sodium orthovanadate,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20826,T3D1768,Vanadium(III) bromide,Protein tyrosine phosphatase type IVA 1,Q93096,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20827,T3D1768,Vanadium(III) bromide,Protein tyrosine phosphatase type IVA 2,Q12974,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20828,T3D1768,Vanadium(III) bromide,Protein tyrosine phosphatase type IVA 3,O75365,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20829,T3D1768,Vanadium(III) bromide,Protein-tyrosine phosphatase mitochondrial 1,Q8WUK0,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20830,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase alpha,P18433,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20831,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase beta,P23467,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20832,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase delta,P23468,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20833,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase epsilon,P23469,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20834,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase eta,Q12913,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20835,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase F,P10586,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20836,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase gamma,P23470,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20837,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase H,Q9HD43,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20838,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase kappa,Q15262,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20839,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase mu,P28827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20840,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase N2,Q92932,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20841,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase O,Q16827,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20842,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase R,Q15256,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20843,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase S,Q13332,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20844,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase T,O14522,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20845,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase U,Q92729 ,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20846,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase zeta,P23471,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20847,T3D1768,Vanadium(III) bromide,Receptor-type tyrosine-protein phosphatase-like N,Q16849,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20848,T3D1768,Vanadium(III) bromide,Sodium/potassium-transporting ATPase gamma chain,P54710,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20849,T3D1768,Vanadium(III) bromide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20850,T3D1768,Vanadium(III) bromide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20851,T3D1768,Vanadium(III) bromide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20852,T3D1768,Vanadium(III) bromide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20853,T3D1768,Vanadium(III) bromide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20854,T3D1768,Vanadium(III) bromide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20855,T3D1768,Vanadium(III) bromide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,"The pentavalent form of vanadium, vanadate, is a potent inhibitor of the Ca+-ATPase and Na+,K+-ATPase of plasma membranes, which decreases intracellular ATP concentration. (S107, S112)"
20856,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 1,P18031,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20857,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 11,Q06124,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20858,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 12,Q05209,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20859,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 13,Q12923,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20860,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 14,Q15678,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20861,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 18,Q99952,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20862,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 2,P17706,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20863,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 20,Q4JDL3,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20864,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 21,Q16825,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20865,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 22,Q9Y2R2,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20866,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 23,Q9H3S7,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20867,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 3,P26045,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20868,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 4,P29074,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20869,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 5,P54829,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20870,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 6,P29350,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20871,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 7,P35236,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20872,T3D1768,Vanadium(III) bromide,Tyrosine-protein phosphatase non-receptor type 9,P43378,"Vanadium inhibits protein tyrosine phosphatases, producing insulin-like effects. (S113)"
20873,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20874,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20875,T3D0754,Cyanogen,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20876,T3D0754,Cyanogen,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20877,T3D0754,Cyanogen,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20878,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20879,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20880,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20881,T3D0754,Cyanogen,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20882,T3D0754,Cyanogen,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20883,T3D0754,Cyanogen,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20884,T3D0754,Cyanogen,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20885,T3D0754,Cyanogen,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20886,T3D0754,Cyanogen,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20887,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20888,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20889,T3D0755,Cyanogen bromide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20890,T3D0755,Cyanogen bromide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20891,T3D0755,Cyanogen bromide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20892,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20893,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20894,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20895,T3D0755,Cyanogen bromide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20896,T3D0755,Cyanogen bromide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20897,T3D0755,Cyanogen bromide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20898,T3D0755,Cyanogen bromide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20899,T3D0755,Cyanogen bromide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20900,T3D0755,Cyanogen bromide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20901,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20902,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20903,T3D0756,Cyanogen chloride,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20904,T3D0756,Cyanogen chloride,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20905,T3D0756,Cyanogen chloride,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20906,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20907,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20908,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20909,T3D0756,Cyanogen chloride,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20910,T3D0756,Cyanogen chloride,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20911,T3D0756,Cyanogen chloride,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20912,T3D0756,Cyanogen chloride,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20913,T3D0756,Cyanogen chloride,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20914,T3D0756,Cyanogen chloride,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20915,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20916,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20917,T3D0758,Cyanogen iodide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20918,T3D0758,Cyanogen iodide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20919,T3D0758,Cyanogen iodide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20920,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20921,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20922,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20923,T3D0758,Cyanogen iodide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20924,T3D0758,Cyanogen iodide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20925,T3D0758,Cyanogen iodide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20926,T3D0758,Cyanogen iodide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20927,T3D0758,Cyanogen iodide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20928,T3D0758,Cyanogen iodide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20929,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20930,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20931,T3D0759,Calcium cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20932,T3D0759,Calcium cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20933,T3D0759,Calcium cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20934,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20935,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20936,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20937,T3D0759,Calcium cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20938,T3D0759,Calcium cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20939,T3D0759,Calcium cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20940,T3D0759,Calcium cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20941,T3D0759,Calcium cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20942,T3D0759,Calcium cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20943,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20944,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20945,T3D0760,Ammonium thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20946,T3D0760,Ammonium thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20947,T3D0760,Ammonium thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20948,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20949,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20950,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20951,T3D0760,Ammonium thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20952,T3D0760,Ammonium thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20953,T3D0760,Ammonium thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20954,T3D0760,Ammonium thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20955,T3D0760,Ammonium thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20956,T3D0760,Ammonium thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20957,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20958,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20959,T3D0761,Potassium cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20960,T3D0761,Potassium cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20961,T3D0761,Potassium cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20962,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20963,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20964,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20965,T3D0761,Potassium cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20966,T3D0761,Potassium cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20967,T3D0761,Potassium cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20968,T3D0761,Potassium cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20969,T3D0761,Potassium cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20970,T3D0761,Potassium cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20971,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20972,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20973,T3D0762,Potassium ferricyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20974,T3D0762,Potassium ferricyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20975,T3D0762,Potassium ferricyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20976,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20977,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20978,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20979,T3D0762,Potassium ferricyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20980,T3D0762,Potassium ferricyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20981,T3D0762,Potassium ferricyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20982,T3D0762,Potassium ferricyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20983,T3D0762,Potassium ferricyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20984,T3D0762,Potassium ferricyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20985,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20986,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20987,T3D0763,Potassium ferrocyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20988,T3D0763,Potassium ferrocyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20989,T3D0763,Potassium ferrocyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20990,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20991,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20992,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20993,T3D0763,Potassium ferrocyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
20994,T3D0763,Potassium ferrocyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
20995,T3D0763,Potassium ferrocyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
20996,T3D0763,Potassium ferrocyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
20997,T3D0763,Potassium ferrocyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
20998,T3D0763,Potassium ferrocyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
20999,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21000,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21001,T3D0764,Potassium silver cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21002,T3D0764,Potassium silver cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21003,T3D0764,Potassium silver cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21004,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21005,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21006,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21007,T3D0764,Potassium silver cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21008,T3D0764,Potassium silver cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21009,T3D0764,Potassium silver cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21010,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21011,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21012,T3D0765,Silver cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21013,T3D0765,Silver cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21014,T3D0765,Silver cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21015,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21016,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21017,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21018,T3D0765,Silver cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21019,T3D0765,Silver cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21020,T3D0765,Silver cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21021,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21022,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21023,T3D0766,Sodium cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21024,T3D0766,Sodium cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21025,T3D0766,Sodium cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21026,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21027,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21028,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21029,T3D0766,Sodium cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21030,T3D0766,Sodium cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21031,T3D0766,Sodium cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21032,T3D0766,Sodium cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21033,T3D0766,Sodium cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21034,T3D0766,Sodium cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21035,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21036,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21037,T3D0767,Sodium ferrocyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21038,T3D0767,Sodium ferrocyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21039,T3D0767,Sodium ferrocyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21040,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21041,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21042,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21043,T3D0767,Sodium ferrocyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21044,T3D0767,Sodium ferrocyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21045,T3D0767,Sodium ferrocyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21046,T3D0767,Sodium ferrocyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21047,T3D0767,Sodium ferrocyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21048,T3D0767,Sodium ferrocyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21049,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21050,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21051,T3D0768,Sodium nitroprusside,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21052,T3D0768,Sodium nitroprusside,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21053,T3D0768,Sodium nitroprusside,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21054,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21055,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21056,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21057,T3D0768,Sodium nitroprusside,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21058,T3D0768,Sodium nitroprusside,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21059,T3D0768,Sodium nitroprusside,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21060,T3D0768,Sodium nitroprusside,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21061,T3D0768,Sodium nitroprusside,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21062,T3D0768,Sodium nitroprusside,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21063,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21064,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21065,T3D0769,Trimethylsilyl cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21066,T3D0769,Trimethylsilyl cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21067,T3D0769,Trimethylsilyl cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21068,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21069,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21070,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21071,T3D0769,Trimethylsilyl cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21072,T3D0769,Trimethylsilyl cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21073,T3D0769,Trimethylsilyl cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21074,T3D0769,Trimethylsilyl cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21075,T3D0769,Trimethylsilyl cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21076,T3D0769,Trimethylsilyl cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21077,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21078,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21079,T3D0776,Potassium cyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21080,T3D0776,Potassium cyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21081,T3D0776,Potassium cyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21082,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21083,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21084,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21085,T3D0776,Potassium cyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21086,T3D0776,Potassium cyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21087,T3D0776,Potassium cyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21088,T3D0776,Potassium cyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21089,T3D0776,Potassium cyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21090,T3D0776,Potassium cyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21091,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21092,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21093,T3D0777,Isocyanic acid,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21094,T3D0777,Isocyanic acid,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21095,T3D0777,Isocyanic acid,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21096,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21097,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21098,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21099,T3D0777,Isocyanic acid,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21100,T3D0777,Isocyanic acid,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21101,T3D0777,Isocyanic acid,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21102,T3D0777,Isocyanic acid,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21103,T3D0777,Isocyanic acid,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21104,T3D0777,Isocyanic acid,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21105,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21106,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21107,T3D0778,Allyl isothiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21108,T3D0778,Allyl isothiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21109,T3D0778,Allyl isothiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21110,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21111,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21112,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21113,T3D0778,Allyl isothiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21114,T3D0778,Allyl isothiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21115,T3D0778,Allyl isothiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21116,T3D0778,Allyl isothiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21117,T3D0778,Allyl isothiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21118,T3D0778,Allyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21119,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21120,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21121,T3D0780,Methyl isothiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21122,T3D0780,Methyl isothiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21123,T3D0780,Methyl isothiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21124,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21125,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21126,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21127,T3D0780,Methyl isothiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21128,T3D0780,Methyl isothiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21129,T3D0780,Methyl isothiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21130,T3D0780,Methyl isothiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21131,T3D0780,Methyl isothiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21132,T3D0780,Methyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21133,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21134,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21135,T3D0781,Phenyl isothiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21136,T3D0781,Phenyl isothiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21137,T3D0781,Phenyl isothiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21138,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21139,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21140,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21141,T3D0781,Phenyl isothiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21142,T3D0781,Phenyl isothiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21143,T3D0781,Phenyl isothiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21144,T3D0781,Phenyl isothiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21145,T3D0781,Phenyl isothiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21146,T3D0781,Phenyl isothiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21147,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21148,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21149,T3D0785,Guanidinium thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21150,T3D0785,Guanidinium thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21151,T3D0785,Guanidinium thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21152,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21153,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21154,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21155,T3D0785,Guanidinium thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21156,T3D0785,Guanidinium thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21157,T3D0785,Guanidinium thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21158,T3D0785,Guanidinium thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21159,T3D0785,Guanidinium thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21160,T3D0785,Guanidinium thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21161,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21162,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21163,T3D0786,Lead thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21164,T3D0786,Lead thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21165,T3D0786,Lead thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21166,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21167,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21168,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21169,T3D0786,Lead thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21170,T3D0786,Lead thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21171,T3D0786,Lead thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21172,T3D0786,Lead thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21173,T3D0786,Lead thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21174,T3D0786,Lead thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21175,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21176,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21177,T3D0787,Potassium thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21178,T3D0787,Potassium thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21179,T3D0787,Potassium thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21180,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21181,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21182,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21183,T3D0787,Potassium thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21184,T3D0787,Potassium thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21185,T3D0787,Potassium thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21186,T3D0787,Potassium thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21187,T3D0787,Potassium thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21188,T3D0787,Potassium thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21189,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21190,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21191,T3D0788,Sodium thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21192,T3D0788,Sodium thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21193,T3D0788,Sodium thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21194,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21195,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21196,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21197,T3D0788,Sodium thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21198,T3D0788,Sodium thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21199,T3D0788,Sodium thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21200,T3D0788,Sodium thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21201,T3D0788,Sodium thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21202,T3D0788,Sodium thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21203,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21204,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21205,T3D0789,Thiocyanic acid,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21206,T3D0789,Thiocyanic acid,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21207,T3D0789,Thiocyanic acid,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21208,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21209,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21210,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21211,T3D0789,Thiocyanic acid,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21212,T3D0789,Thiocyanic acid,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21213,T3D0789,Thiocyanic acid,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21214,T3D0789,Thiocyanic acid,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21215,T3D0789,Thiocyanic acid,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21216,T3D0789,Thiocyanic acid,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21217,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21218,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21219,T3D0790,Cyanuric acid,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21220,T3D0790,Cyanuric acid,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21221,T3D0790,Cyanuric acid,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21222,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21223,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21224,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21225,T3D0790,Cyanuric acid,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21226,T3D0790,Cyanuric acid,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21227,T3D0790,Cyanuric acid,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21228,T3D0790,Cyanuric acid,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21229,T3D0790,Cyanuric acid,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21230,T3D0790,Cyanuric acid,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21231,T3D1103,Barium cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21232,T3D1103,Barium cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21233,T3D1103,Barium cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21234,T3D1103,Barium cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21235,T3D1103,Barium cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21236,T3D1103,Barium cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21237,T3D1103,Barium cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21238,T3D1103,Barium cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21239,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21240,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21241,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21242,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21243,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21244,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21245,T3D1103,Barium cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21246,T3D1103,Barium cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21247,T3D1103,Barium cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21248,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21249,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21250,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21251,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21252,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21253,T3D1103,Barium cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21254,T3D1103,Barium cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21255,T3D1103,Barium cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21256,T3D1103,Barium cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21257,T3D1103,Barium cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21258,T3D1103,Barium cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21259,T3D1103,Barium cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21260,T3D1103,Barium cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21261,T3D1103,Barium cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21262,T3D1103,Barium cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21263,T3D1103,Barium cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21264,T3D1103,Barium cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21265,T3D1103,Barium cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21266,T3D1103,Barium cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21267,T3D1103,Barium cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21268,T3D1103,Barium cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21269,T3D1103,Barium cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21270,T3D1147,Manganese phthalocyanine,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21271,T3D1147,Manganese phthalocyanine,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21272,T3D1147,Manganese phthalocyanine,Catalase,P04040,Cyanide inhibits catalase. (R211)
21273,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21274,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21275,T3D1147,Manganese phthalocyanine,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21276,T3D1147,Manganese phthalocyanine,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21277,T3D1147,Manganese phthalocyanine,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21278,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21279,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21280,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21281,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21282,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21283,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21284,T3D1147,Manganese phthalocyanine,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21285,T3D1147,Manganese phthalocyanine,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21286,T3D1147,Manganese phthalocyanine,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21287,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21288,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21289,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21290,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21291,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21292,T3D1147,Manganese phthalocyanine,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21293,T3D1147,Manganese phthalocyanine,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21294,T3D1147,Manganese phthalocyanine,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21295,T3D1147,Manganese phthalocyanine,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21296,T3D1147,Manganese phthalocyanine,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21297,T3D1147,Manganese phthalocyanine,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21298,T3D1147,Manganese phthalocyanine,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21299,T3D1147,Manganese phthalocyanine,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21300,T3D1147,Manganese phthalocyanine,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21301,T3D1147,Manganese phthalocyanine,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21302,T3D1147,Manganese phthalocyanine,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21303,T3D1147,Manganese phthalocyanine,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21304,T3D1147,Manganese phthalocyanine,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21305,T3D1147,Manganese phthalocyanine,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21306,T3D1147,Manganese phthalocyanine,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21307,T3D1147,Manganese phthalocyanine,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21308,T3D1147,Manganese phthalocyanine,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21309,T3D1347,Mercuric potassium cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21310,T3D1347,Mercuric potassium cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
21311,T3D1347,Mercuric potassium cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21312,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21313,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21314,T3D1347,Mercuric potassium cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21315,T3D1347,Mercuric potassium cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21316,T3D1347,Mercuric potassium cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21317,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21318,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21319,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21320,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21321,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21322,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21323,T3D1347,Mercuric potassium cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21324,T3D1347,Mercuric potassium cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21325,T3D1347,Mercuric potassium cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21326,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21327,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21328,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21329,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21330,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21331,T3D1347,Mercuric potassium cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21332,T3D1347,Mercuric potassium cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21333,T3D1347,Mercuric potassium cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21334,T3D1347,Mercuric potassium cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21335,T3D1347,Mercuric potassium cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21336,T3D1347,Mercuric potassium cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21337,T3D1347,Mercuric potassium cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21338,T3D1347,Mercuric potassium cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21339,T3D1347,Mercuric potassium cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21340,T3D1347,Mercuric potassium cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21341,T3D1347,Mercuric potassium cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21342,T3D1347,Mercuric potassium cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21343,T3D1347,Mercuric potassium cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21344,T3D1347,Mercuric potassium cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21345,T3D1347,Mercuric potassium cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21346,T3D1347,Mercuric potassium cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21347,T3D1347,Mercuric potassium cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21348,T3D1350,Methylmercuric dicyanamide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21349,T3D1350,Methylmercuric dicyanamide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
21350,T3D1350,Methylmercuric dicyanamide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21351,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21352,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21353,T3D1350,Methylmercuric dicyanamide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21354,T3D1350,Methylmercuric dicyanamide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21355,T3D1350,Methylmercuric dicyanamide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21356,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21357,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21358,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21359,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21360,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21361,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21362,T3D1350,Methylmercuric dicyanamide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21363,T3D1350,Methylmercuric dicyanamide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21364,T3D1350,Methylmercuric dicyanamide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21365,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21366,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21367,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21368,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21369,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21370,T3D1350,Methylmercuric dicyanamide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21371,T3D1350,Methylmercuric dicyanamide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21372,T3D1350,Methylmercuric dicyanamide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21373,T3D1350,Methylmercuric dicyanamide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21374,T3D1350,Methylmercuric dicyanamide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21375,T3D1350,Methylmercuric dicyanamide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21376,T3D1350,Methylmercuric dicyanamide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21377,T3D1350,Methylmercuric dicyanamide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21378,T3D1350,Methylmercuric dicyanamide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21379,T3D1350,Methylmercuric dicyanamide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21380,T3D1350,Methylmercuric dicyanamide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21381,T3D1350,Methylmercuric dicyanamide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21382,T3D1350,Methylmercuric dicyanamide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21383,T3D1350,Methylmercuric dicyanamide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21384,T3D1350,Methylmercuric dicyanamide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21385,T3D1350,Methylmercuric dicyanamide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21386,T3D1350,Methylmercuric dicyanamide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21387,T3D1372,Cadmium cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21388,T3D1372,Cadmium cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21389,T3D1372,Cadmium cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21390,T3D1372,Cadmium cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21391,T3D1372,Cadmium cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21392,T3D1372,Cadmium cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21393,T3D1372,Cadmium cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21394,T3D1372,Cadmium cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21395,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21396,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21397,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21398,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21399,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21400,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21401,T3D1372,Cadmium cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21402,T3D1372,Cadmium cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21403,T3D1372,Cadmium cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21404,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21405,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21406,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21407,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21408,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21409,T3D1372,Cadmium cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21410,T3D1372,Cadmium cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21411,T3D1372,Cadmium cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21412,T3D1372,Cadmium cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21413,T3D1372,Cadmium cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21414,T3D1372,Cadmium cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21415,T3D1372,Cadmium cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21416,T3D1372,Cadmium cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21417,T3D1372,Cadmium cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21418,T3D1372,Cadmium cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21419,T3D1372,Cadmium cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21420,T3D1372,Cadmium cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21421,T3D1372,Cadmium cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21422,T3D1372,Cadmium cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21423,T3D1372,Cadmium cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21424,T3D1372,Cadmium cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21425,T3D1372,Cadmium cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21426,T3D1395,Cobalt(II) cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21427,T3D1395,Cobalt(II) cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21428,T3D1395,Cobalt(II) cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21429,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21430,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21431,T3D1395,Cobalt(II) cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21432,T3D1395,Cobalt(II) cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21433,T3D1395,Cobalt(II) cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21434,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21435,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21436,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21437,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21438,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21439,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21440,T3D1395,Cobalt(II) cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21441,T3D1395,Cobalt(II) cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21442,T3D1395,Cobalt(II) cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21443,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21444,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21445,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21446,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21447,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21448,T3D1395,Cobalt(II) cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21449,T3D1395,Cobalt(II) cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21450,T3D1395,Cobalt(II) cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21451,T3D1395,Cobalt(II) cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21452,T3D1395,Cobalt(II) cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21453,T3D1395,Cobalt(II) cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21454,T3D1395,Cobalt(II) cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21455,T3D1395,Cobalt(II) cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21456,T3D1395,Cobalt(II) cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21457,T3D1395,Cobalt(II) cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21458,T3D1395,Cobalt(II) cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21459,T3D1395,Cobalt(II) cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21460,T3D1395,Cobalt(II) cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21461,T3D1395,Cobalt(II) cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21462,T3D1395,Cobalt(II) cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21463,T3D1395,Cobalt(II) cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21464,T3D1395,Cobalt(II) cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21465,T3D1396,Cobalt(II) cyanide dihydrate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21466,T3D1396,Cobalt(II) cyanide dihydrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21467,T3D1396,Cobalt(II) cyanide dihydrate,Catalase,P04040,Cyanide inhibits catalase. (R211)
21468,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21469,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21470,T3D1396,Cobalt(II) cyanide dihydrate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21471,T3D1396,Cobalt(II) cyanide dihydrate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21472,T3D1396,Cobalt(II) cyanide dihydrate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21473,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21474,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21475,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21476,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21477,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21478,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21479,T3D1396,Cobalt(II) cyanide dihydrate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21480,T3D1396,Cobalt(II) cyanide dihydrate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21481,T3D1396,Cobalt(II) cyanide dihydrate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21482,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21483,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21484,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21485,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21486,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21487,T3D1396,Cobalt(II) cyanide dihydrate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21488,T3D1396,Cobalt(II) cyanide dihydrate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21489,T3D1396,Cobalt(II) cyanide dihydrate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21490,T3D1396,Cobalt(II) cyanide dihydrate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21491,T3D1396,Cobalt(II) cyanide dihydrate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21492,T3D1396,Cobalt(II) cyanide dihydrate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21493,T3D1396,Cobalt(II) cyanide dihydrate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21494,T3D1396,Cobalt(II) cyanide dihydrate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21495,T3D1396,Cobalt(II) cyanide dihydrate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21496,T3D1396,Cobalt(II) cyanide dihydrate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21497,T3D1396,Cobalt(II) cyanide dihydrate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21498,T3D1396,Cobalt(II) cyanide dihydrate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21499,T3D1396,Cobalt(II) cyanide dihydrate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21500,T3D1396,Cobalt(II) cyanide dihydrate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21501,T3D1396,Cobalt(II) cyanide dihydrate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21502,T3D1396,Cobalt(II) cyanide dihydrate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21503,T3D1396,Cobalt(II) cyanide dihydrate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21504,T3D1397,Cobalt(II) cyanide trihydrate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21505,T3D1397,Cobalt(II) cyanide trihydrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21506,T3D1397,Cobalt(II) cyanide trihydrate,Catalase,P04040,Cyanide inhibits catalase. (R211)
21507,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21508,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21509,T3D1397,Cobalt(II) cyanide trihydrate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21510,T3D1397,Cobalt(II) cyanide trihydrate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21511,T3D1397,Cobalt(II) cyanide trihydrate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21512,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21513,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21514,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21515,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21516,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21517,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21518,T3D1397,Cobalt(II) cyanide trihydrate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21519,T3D1397,Cobalt(II) cyanide trihydrate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21520,T3D1397,Cobalt(II) cyanide trihydrate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21521,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21522,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21523,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21524,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21525,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21526,T3D1397,Cobalt(II) cyanide trihydrate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21527,T3D1397,Cobalt(II) cyanide trihydrate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21528,T3D1397,Cobalt(II) cyanide trihydrate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21529,T3D1397,Cobalt(II) cyanide trihydrate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21530,T3D1397,Cobalt(II) cyanide trihydrate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21531,T3D1397,Cobalt(II) cyanide trihydrate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21532,T3D1397,Cobalt(II) cyanide trihydrate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21533,T3D1397,Cobalt(II) cyanide trihydrate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21534,T3D1397,Cobalt(II) cyanide trihydrate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21535,T3D1397,Cobalt(II) cyanide trihydrate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21536,T3D1397,Cobalt(II) cyanide trihydrate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21537,T3D1397,Cobalt(II) cyanide trihydrate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21538,T3D1397,Cobalt(II) cyanide trihydrate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21539,T3D1397,Cobalt(II) cyanide trihydrate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21540,T3D1397,Cobalt(II) cyanide trihydrate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21541,T3D1397,Cobalt(II) cyanide trihydrate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21542,T3D1397,Cobalt(II) cyanide trihydrate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21543,T3D1422,Nickel potassium cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21544,T3D1422,Nickel potassium cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21545,T3D1422,Nickel potassium cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21546,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21547,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21548,T3D1422,Nickel potassium cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21549,T3D1422,Nickel potassium cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21550,T3D1422,Nickel potassium cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21551,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21552,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21553,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21554,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21555,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21556,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21557,T3D1422,Nickel potassium cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21558,T3D1422,Nickel potassium cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21559,T3D1422,Nickel potassium cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21560,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21561,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21562,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21563,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21564,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21565,T3D1422,Nickel potassium cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21566,T3D1422,Nickel potassium cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21567,T3D1422,Nickel potassium cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21568,T3D1422,Nickel potassium cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21569,T3D1422,Nickel potassium cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21570,T3D1422,Nickel potassium cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21571,T3D1422,Nickel potassium cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21572,T3D1422,Nickel potassium cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21573,T3D1422,Nickel potassium cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21574,T3D1422,Nickel potassium cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21575,T3D1422,Nickel potassium cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21576,T3D1422,Nickel potassium cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21577,T3D1422,Nickel potassium cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21578,T3D1422,Nickel potassium cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21579,T3D1422,Nickel potassium cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21580,T3D1422,Nickel potassium cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21581,T3D1422,Nickel potassium cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21582,T3D0746,Zinc thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21583,T3D0746,Zinc thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21584,T3D0746,Zinc thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
21585,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21586,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21587,T3D0746,Zinc thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21588,T3D0746,Zinc thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21589,T3D0746,Zinc thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21590,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21591,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21592,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21593,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21594,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21595,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21596,T3D0746,Zinc thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21597,T3D0746,Zinc thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21598,T3D0746,Zinc thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21599,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21600,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21601,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21602,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21603,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21604,T3D0746,Zinc thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21605,T3D0746,Zinc thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21606,T3D0746,Zinc thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21607,T3D0746,Zinc thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21608,T3D0746,Zinc thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21609,T3D0746,Zinc thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21610,T3D0746,Zinc thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21611,T3D0746,Zinc thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21612,T3D0746,Zinc thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21613,T3D0746,Zinc thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21614,T3D0746,Zinc thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21615,T3D0746,Zinc thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21616,T3D0746,Zinc thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21617,T3D0746,Zinc thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21618,T3D0746,Zinc thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21619,T3D0746,Zinc thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21620,T3D1648,Palladium(II) cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21621,T3D1648,Palladium(II) cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21622,T3D1648,Palladium(II) cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21623,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21624,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21625,T3D1648,Palladium(II) cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21626,T3D1648,Palladium(II) cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21627,T3D1648,Palladium(II) cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21628,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21629,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21630,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21631,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21632,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21633,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21634,T3D1648,Palladium(II) cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21635,T3D1648,Palladium(II) cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21636,T3D1648,Palladium(II) cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21637,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21638,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21639,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21640,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21641,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21642,T3D1648,Palladium(II) cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21643,T3D1648,Palladium(II) cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21644,T3D1648,Palladium(II) cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21645,T3D1648,Palladium(II) cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21646,T3D1648,Palladium(II) cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21647,T3D1648,Palladium(II) cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21648,T3D1648,Palladium(II) cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21649,T3D1648,Palladium(II) cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21650,T3D1648,Palladium(II) cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21651,T3D1648,Palladium(II) cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21652,T3D1648,Palladium(II) cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21653,T3D1648,Palladium(II) cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21654,T3D1648,Palladium(II) cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21655,T3D1648,Palladium(II) cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21656,T3D1648,Palladium(II) cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21657,T3D1648,Palladium(II) cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21658,T3D1648,Palladium(II) cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21659,T3D1649,Fluorescein isothiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21660,T3D1649,Fluorescein isothiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21661,T3D1649,Fluorescein isothiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
21662,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21663,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21664,T3D1649,Fluorescein isothiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21665,T3D1649,Fluorescein isothiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21666,T3D1649,Fluorescein isothiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21667,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21668,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21669,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21670,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21671,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21672,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21673,T3D1649,Fluorescein isothiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21674,T3D1649,Fluorescein isothiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21675,T3D1649,Fluorescein isothiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21676,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21677,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21678,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21679,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21680,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21681,T3D1649,Fluorescein isothiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21682,T3D1649,Fluorescein isothiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21683,T3D1649,Fluorescein isothiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21684,T3D1649,Fluorescein isothiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21685,T3D1649,Fluorescein isothiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21686,T3D1649,Fluorescein isothiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21687,T3D1649,Fluorescein isothiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21688,T3D1649,Fluorescein isothiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21689,T3D1649,Fluorescein isothiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21690,T3D1649,Fluorescein isothiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21691,T3D1649,Fluorescein isothiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21692,T3D1649,Fluorescein isothiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21693,T3D1649,Fluorescein isothiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21694,T3D1649,Fluorescein isothiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21695,T3D1649,Fluorescein isothiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21696,T3D1649,Fluorescein isothiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21697,T3D1649,Fluorescein isothiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21698,T3D1650,tert-Butyl isocyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21699,T3D1650,tert-Butyl isocyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21700,T3D1650,tert-Butyl isocyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21701,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21702,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21703,T3D1650,tert-Butyl isocyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21704,T3D1650,tert-Butyl isocyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21705,T3D1650,tert-Butyl isocyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21706,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21707,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21708,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21709,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21710,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21711,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21712,T3D1650,tert-Butyl isocyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21713,T3D1650,tert-Butyl isocyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21714,T3D1650,tert-Butyl isocyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21715,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21716,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21717,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21718,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21719,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21720,T3D1650,tert-Butyl isocyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21721,T3D1650,tert-Butyl isocyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21722,T3D1650,tert-Butyl isocyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21723,T3D1650,tert-Butyl isocyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21724,T3D1650,tert-Butyl isocyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21725,T3D1650,tert-Butyl isocyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21726,T3D1650,tert-Butyl isocyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21727,T3D1650,tert-Butyl isocyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21728,T3D1650,tert-Butyl isocyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21729,T3D1650,tert-Butyl isocyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21730,T3D1650,tert-Butyl isocyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21731,T3D1650,tert-Butyl isocyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21732,T3D1650,tert-Butyl isocyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21733,T3D1650,tert-Butyl isocyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21734,T3D1650,tert-Butyl isocyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21735,T3D1650,tert-Butyl isocyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21736,T3D1650,tert-Butyl isocyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21737,T3D1651,Hydrogen isocyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21738,T3D1651,Hydrogen isocyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21739,T3D1651,Hydrogen isocyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21740,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21741,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21742,T3D1651,Hydrogen isocyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21743,T3D1651,Hydrogen isocyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21744,T3D1651,Hydrogen isocyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21745,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21746,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21747,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21748,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21749,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21750,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21751,T3D1651,Hydrogen isocyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21752,T3D1651,Hydrogen isocyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21753,T3D1651,Hydrogen isocyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21754,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21755,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21756,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21757,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21758,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21759,T3D1651,Hydrogen isocyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21760,T3D1651,Hydrogen isocyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21761,T3D1651,Hydrogen isocyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21762,T3D1651,Hydrogen isocyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21763,T3D1651,Hydrogen isocyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21764,T3D1651,Hydrogen isocyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21765,T3D1651,Hydrogen isocyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21766,T3D1651,Hydrogen isocyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21767,T3D1651,Hydrogen isocyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21768,T3D1651,Hydrogen isocyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21769,T3D1651,Hydrogen isocyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21770,T3D1651,Hydrogen isocyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21771,T3D1651,Hydrogen isocyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21772,T3D1651,Hydrogen isocyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21773,T3D1651,Hydrogen isocyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21774,T3D1651,Hydrogen isocyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21775,T3D1651,Hydrogen isocyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21776,T3D1652,Methyl isocyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21777,T3D1652,Methyl isocyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21778,T3D1652,Methyl isocyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21779,T3D1652,Methyl isocyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21780,T3D1652,Methyl isocyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21781,T3D1652,Methyl isocyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21782,T3D1652,Methyl isocyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21783,T3D1652,Methyl isocyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21784,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21785,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21786,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21787,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21788,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21789,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21790,T3D1652,Methyl isocyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21791,T3D1652,Methyl isocyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21792,T3D1652,Methyl isocyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21793,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21794,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21795,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21796,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21797,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21798,T3D1652,Methyl isocyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21799,T3D1652,Methyl isocyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21800,T3D1652,Methyl isocyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21801,T3D1652,Methyl isocyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21802,T3D1652,Methyl isocyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21803,T3D1652,Methyl isocyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21804,T3D1652,Methyl isocyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21805,T3D1652,Methyl isocyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21806,T3D1652,Methyl isocyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21807,T3D1652,Methyl isocyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21808,T3D1652,Methyl isocyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21809,T3D1652,Methyl isocyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21810,T3D1652,Methyl isocyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21811,T3D1652,Methyl isocyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21812,T3D1652,Methyl isocyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21813,T3D1652,Methyl isocyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21814,T3D1652,Methyl isocyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21815,T3D1653,Toluenesulfonylmethyl isocyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21816,T3D1653,Toluenesulfonylmethyl isocyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21817,T3D1653,Toluenesulfonylmethyl isocyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21818,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21819,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21820,T3D1653,Toluenesulfonylmethyl isocyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21821,T3D1653,Toluenesulfonylmethyl isocyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21822,T3D1653,Toluenesulfonylmethyl isocyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21823,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21824,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21825,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21826,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21827,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21828,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21829,T3D1653,Toluenesulfonylmethyl isocyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21830,T3D1653,Toluenesulfonylmethyl isocyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21831,T3D1653,Toluenesulfonylmethyl isocyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21832,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21833,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21834,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21835,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21836,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21837,T3D1653,Toluenesulfonylmethyl isocyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21838,T3D1653,Toluenesulfonylmethyl isocyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21839,T3D1653,Toluenesulfonylmethyl isocyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21840,T3D1653,Toluenesulfonylmethyl isocyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21841,T3D1653,Toluenesulfonylmethyl isocyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21842,T3D1653,Toluenesulfonylmethyl isocyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21843,T3D1653,Toluenesulfonylmethyl isocyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21844,T3D1653,Toluenesulfonylmethyl isocyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21845,T3D1653,Toluenesulfonylmethyl isocyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21846,T3D1653,Toluenesulfonylmethyl isocyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21847,T3D1653,Toluenesulfonylmethyl isocyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21848,T3D1653,Toluenesulfonylmethyl isocyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21849,T3D1653,Toluenesulfonylmethyl isocyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21850,T3D1653,Toluenesulfonylmethyl isocyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21851,T3D1653,Toluenesulfonylmethyl isocyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21852,T3D1653,Toluenesulfonylmethyl isocyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21853,T3D1653,Toluenesulfonylmethyl isocyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21854,T3D1654,Trifluoromethyl isocyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21855,T3D1654,Trifluoromethyl isocyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21856,T3D1654,Trifluoromethyl isocyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
21857,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21858,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21859,T3D1654,Trifluoromethyl isocyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21860,T3D1654,Trifluoromethyl isocyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21861,T3D1654,Trifluoromethyl isocyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21862,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21863,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21864,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21865,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21866,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21867,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21868,T3D1654,Trifluoromethyl isocyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21869,T3D1654,Trifluoromethyl isocyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21870,T3D1654,Trifluoromethyl isocyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21871,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21872,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21873,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21874,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21875,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21876,T3D1654,Trifluoromethyl isocyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21877,T3D1654,Trifluoromethyl isocyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21878,T3D1654,Trifluoromethyl isocyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21879,T3D1654,Trifluoromethyl isocyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21880,T3D1654,Trifluoromethyl isocyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21881,T3D1654,Trifluoromethyl isocyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21882,T3D1654,Trifluoromethyl isocyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21883,T3D1654,Trifluoromethyl isocyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21884,T3D1654,Trifluoromethyl isocyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21885,T3D1654,Trifluoromethyl isocyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21886,T3D1654,Trifluoromethyl isocyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21887,T3D1654,Trifluoromethyl isocyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21888,T3D1654,Trifluoromethyl isocyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21889,T3D1654,Trifluoromethyl isocyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21890,T3D1654,Trifluoromethyl isocyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21891,T3D1654,Trifluoromethyl isocyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21892,T3D1654,Trifluoromethyl isocyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21893,T3D1655,Xantocillin,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21894,T3D1655,Xantocillin,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21895,T3D1655,Xantocillin,Catalase,P04040,Cyanide inhibits catalase. (R211)
21896,T3D1655,Xantocillin,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21897,T3D1655,Xantocillin,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21898,T3D1655,Xantocillin,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21899,T3D1655,Xantocillin,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21900,T3D1655,Xantocillin,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21901,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21902,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21903,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21904,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21905,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21906,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21907,T3D1655,Xantocillin,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21908,T3D1655,Xantocillin,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21909,T3D1655,Xantocillin,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21910,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21911,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21912,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21913,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21914,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21915,T3D1655,Xantocillin,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21916,T3D1655,Xantocillin,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21917,T3D1655,Xantocillin,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21918,T3D1655,Xantocillin,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21919,T3D1655,Xantocillin,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21920,T3D1655,Xantocillin,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21921,T3D1655,Xantocillin,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21922,T3D1655,Xantocillin,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21923,T3D1655,Xantocillin,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21924,T3D1655,Xantocillin,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21925,T3D1655,Xantocillin,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21926,T3D1655,Xantocillin,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21927,T3D1655,Xantocillin,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21928,T3D1655,Xantocillin,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21929,T3D1655,Xantocillin,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21930,T3D1655,Xantocillin,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21931,T3D1655,Xantocillin,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21932,T3D1656,Potassium ferrocyanide trihydrate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21933,T3D1656,Potassium ferrocyanide trihydrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21934,T3D1656,Potassium ferrocyanide trihydrate,Catalase,P04040,Cyanide inhibits catalase. (R211)
21935,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21936,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21937,T3D1656,Potassium ferrocyanide trihydrate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21938,T3D1656,Potassium ferrocyanide trihydrate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21939,T3D1656,Potassium ferrocyanide trihydrate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21940,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21941,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21942,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21943,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21944,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21945,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21946,T3D1656,Potassium ferrocyanide trihydrate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21947,T3D1656,Potassium ferrocyanide trihydrate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21948,T3D1656,Potassium ferrocyanide trihydrate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21949,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21950,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21951,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21952,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21953,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21954,T3D1656,Potassium ferrocyanide trihydrate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21955,T3D1656,Potassium ferrocyanide trihydrate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21956,T3D1656,Potassium ferrocyanide trihydrate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21957,T3D1656,Potassium ferrocyanide trihydrate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21958,T3D1656,Potassium ferrocyanide trihydrate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21959,T3D1656,Potassium ferrocyanide trihydrate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21960,T3D1656,Potassium ferrocyanide trihydrate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
21961,T3D1656,Potassium ferrocyanide trihydrate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
21962,T3D1656,Potassium ferrocyanide trihydrate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
21963,T3D1656,Potassium ferrocyanide trihydrate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
21964,T3D1656,Potassium ferrocyanide trihydrate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
21965,T3D1656,Potassium ferrocyanide trihydrate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
21966,T3D1656,Potassium ferrocyanide trihydrate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
21967,T3D1656,Potassium ferrocyanide trihydrate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
21968,T3D1656,Potassium ferrocyanide trihydrate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
21969,T3D1656,Potassium ferrocyanide trihydrate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21970,T3D1656,Potassium ferrocyanide trihydrate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
21971,T3D1657,Sodium ferrocyanide decahydrate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
21972,T3D1657,Sodium ferrocyanide decahydrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
21973,T3D1657,Sodium ferrocyanide decahydrate,Catalase,P04040,Cyanide inhibits catalase. (R211)
21974,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21975,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21976,T3D1657,Sodium ferrocyanide decahydrate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21977,T3D1657,Sodium ferrocyanide decahydrate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21978,T3D1657,Sodium ferrocyanide decahydrate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21979,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21980,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21981,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21982,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21983,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21984,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21985,T3D1657,Sodium ferrocyanide decahydrate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21986,T3D1657,Sodium ferrocyanide decahydrate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21987,T3D1657,Sodium ferrocyanide decahydrate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21988,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21989,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21990,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21991,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21992,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21993,T3D1657,Sodium ferrocyanide decahydrate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
21994,T3D1657,Sodium ferrocyanide decahydrate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
21995,T3D1657,Sodium ferrocyanide decahydrate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
21996,T3D1657,Sodium ferrocyanide decahydrate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
21997,T3D1657,Sodium ferrocyanide decahydrate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
21998,T3D1657,Sodium ferrocyanide decahydrate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
21999,T3D1657,Sodium ferrocyanide decahydrate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22000,T3D1657,Sodium ferrocyanide decahydrate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22001,T3D1657,Sodium ferrocyanide decahydrate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22002,T3D1657,Sodium ferrocyanide decahydrate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22003,T3D1657,Sodium ferrocyanide decahydrate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22004,T3D1657,Sodium ferrocyanide decahydrate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22005,T3D1657,Sodium ferrocyanide decahydrate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22006,T3D1657,Sodium ferrocyanide decahydrate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22007,T3D1657,Sodium ferrocyanide decahydrate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22008,T3D1657,Sodium ferrocyanide decahydrate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22009,T3D1657,Sodium ferrocyanide decahydrate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22010,T3D1658,Sodium nitroprusside dihydrate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22011,T3D1658,Sodium nitroprusside dihydrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22012,T3D1658,Sodium nitroprusside dihydrate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22013,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22014,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22015,T3D1658,Sodium nitroprusside dihydrate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22016,T3D1658,Sodium nitroprusside dihydrate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22017,T3D1658,Sodium nitroprusside dihydrate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22018,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22019,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22020,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22021,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22022,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22023,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22024,T3D1658,Sodium nitroprusside dihydrate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22025,T3D1658,Sodium nitroprusside dihydrate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22026,T3D1658,Sodium nitroprusside dihydrate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22027,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22028,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22029,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22030,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22031,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22032,T3D1658,Sodium nitroprusside dihydrate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22033,T3D1658,Sodium nitroprusside dihydrate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22034,T3D1658,Sodium nitroprusside dihydrate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22035,T3D1658,Sodium nitroprusside dihydrate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22036,T3D1658,Sodium nitroprusside dihydrate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22037,T3D1658,Sodium nitroprusside dihydrate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22038,T3D1658,Sodium nitroprusside dihydrate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22039,T3D1658,Sodium nitroprusside dihydrate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22040,T3D1658,Sodium nitroprusside dihydrate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22041,T3D1658,Sodium nitroprusside dihydrate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22042,T3D1658,Sodium nitroprusside dihydrate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22043,T3D1658,Sodium nitroprusside dihydrate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22044,T3D1658,Sodium nitroprusside dihydrate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22045,T3D1658,Sodium nitroprusside dihydrate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22046,T3D1658,Sodium nitroprusside dihydrate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22047,T3D1658,Sodium nitroprusside dihydrate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22048,T3D1658,Sodium nitroprusside dihydrate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22049,T3D1659,Phenyl isocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22050,T3D1659,Phenyl isocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22051,T3D1659,Phenyl isocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22052,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22053,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22054,T3D1659,Phenyl isocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22055,T3D1659,Phenyl isocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22056,T3D1659,Phenyl isocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22057,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22058,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22059,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22060,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22061,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22062,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22063,T3D1659,Phenyl isocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22064,T3D1659,Phenyl isocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22065,T3D1659,Phenyl isocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22066,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22067,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22068,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22069,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22070,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22071,T3D1659,Phenyl isocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22072,T3D1659,Phenyl isocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22073,T3D1659,Phenyl isocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22074,T3D1659,Phenyl isocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22075,T3D1659,Phenyl isocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22076,T3D1659,Phenyl isocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22077,T3D1659,Phenyl isocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22078,T3D1659,Phenyl isocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22079,T3D1659,Phenyl isocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22080,T3D1659,Phenyl isocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22081,T3D1659,Phenyl isocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22082,T3D1659,Phenyl isocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22083,T3D1659,Phenyl isocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22084,T3D1659,Phenyl isocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22085,T3D1659,Phenyl isocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22086,T3D1659,Phenyl isocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22087,T3D1659,Phenyl isocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22088,T3D1660,Chlorosulfonyl isocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22089,T3D1660,Chlorosulfonyl isocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22090,T3D1660,Chlorosulfonyl isocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22091,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22092,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22093,T3D1660,Chlorosulfonyl isocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22094,T3D1660,Chlorosulfonyl isocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22095,T3D1660,Chlorosulfonyl isocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22096,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22097,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22098,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22099,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22100,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22101,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22102,T3D1660,Chlorosulfonyl isocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22103,T3D1660,Chlorosulfonyl isocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22104,T3D1660,Chlorosulfonyl isocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22105,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22106,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22107,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22108,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22109,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22110,T3D1660,Chlorosulfonyl isocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22111,T3D1660,Chlorosulfonyl isocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22112,T3D1660,Chlorosulfonyl isocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22113,T3D1660,Chlorosulfonyl isocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22114,T3D1660,Chlorosulfonyl isocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22115,T3D1660,Chlorosulfonyl isocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22116,T3D1660,Chlorosulfonyl isocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22117,T3D1660,Chlorosulfonyl isocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22118,T3D1660,Chlorosulfonyl isocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22119,T3D1660,Chlorosulfonyl isocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22120,T3D1660,Chlorosulfonyl isocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22121,T3D1660,Chlorosulfonyl isocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22122,T3D1660,Chlorosulfonyl isocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22123,T3D1660,Chlorosulfonyl isocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22124,T3D1660,Chlorosulfonyl isocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22125,T3D1660,Chlorosulfonyl isocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22126,T3D1660,Chlorosulfonyl isocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22127,T3D1661,Hexamethylene diisocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22128,T3D1661,Hexamethylene diisocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22129,T3D1661,Hexamethylene diisocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22130,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22131,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22132,T3D1661,Hexamethylene diisocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22133,T3D1661,Hexamethylene diisocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22134,T3D1661,Hexamethylene diisocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22135,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22136,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22137,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22138,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22139,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22140,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22141,T3D1661,Hexamethylene diisocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22142,T3D1661,Hexamethylene diisocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22143,T3D1661,Hexamethylene diisocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22144,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22145,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22146,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22147,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22148,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22149,T3D1661,Hexamethylene diisocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22150,T3D1661,Hexamethylene diisocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22151,T3D1661,Hexamethylene diisocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22152,T3D1661,Hexamethylene diisocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22153,T3D1661,Hexamethylene diisocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22154,T3D1661,Hexamethylene diisocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22155,T3D1661,Hexamethylene diisocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22156,T3D1661,Hexamethylene diisocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22157,T3D1661,Hexamethylene diisocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22158,T3D1661,Hexamethylene diisocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22159,T3D1661,Hexamethylene diisocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22160,T3D1661,Hexamethylene diisocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22161,T3D1661,Hexamethylene diisocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22162,T3D1661,Hexamethylene diisocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22163,T3D1661,Hexamethylene diisocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22164,T3D1661,Hexamethylene diisocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22165,T3D1661,Hexamethylene diisocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22166,T3D1662,Isophorone diisocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22167,T3D1662,Isophorone diisocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22168,T3D1662,Isophorone diisocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22169,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22170,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22171,T3D1662,Isophorone diisocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22172,T3D1662,Isophorone diisocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22173,T3D1662,Isophorone diisocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22174,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22175,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22176,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22177,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22178,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22179,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22180,T3D1662,Isophorone diisocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22181,T3D1662,Isophorone diisocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22182,T3D1662,Isophorone diisocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22183,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22184,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22185,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22186,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22187,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22188,T3D1662,Isophorone diisocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22189,T3D1662,Isophorone diisocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22190,T3D1662,Isophorone diisocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22191,T3D1662,Isophorone diisocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22192,T3D1662,Isophorone diisocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22193,T3D1662,Isophorone diisocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22194,T3D1662,Isophorone diisocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22195,T3D1662,Isophorone diisocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22196,T3D1662,Isophorone diisocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22197,T3D1662,Isophorone diisocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22198,T3D1662,Isophorone diisocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22199,T3D1662,Isophorone diisocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22200,T3D1662,Isophorone diisocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22201,T3D1662,Isophorone diisocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22202,T3D1662,Isophorone diisocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22203,T3D1662,Isophorone diisocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22204,T3D1662,Isophorone diisocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22205,T3D1663,Methyl isocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22206,T3D1663,Methyl isocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22207,T3D1663,Methyl isocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22208,T3D1663,Methyl isocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22209,T3D1663,Methyl isocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22210,T3D1663,Methyl isocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22211,T3D1663,Methyl isocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22212,T3D1663,Methyl isocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22213,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22214,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22215,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22216,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22217,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22218,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22219,T3D1663,Methyl isocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22220,T3D1663,Methyl isocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22221,T3D1663,Methyl isocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22222,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22223,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22224,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22225,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22226,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22227,T3D1663,Methyl isocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22228,T3D1663,Methyl isocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22229,T3D1663,Methyl isocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22230,T3D1663,Methyl isocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22231,T3D1663,Methyl isocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22232,T3D1663,Methyl isocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22233,T3D1663,Methyl isocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22234,T3D1663,Methyl isocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22235,T3D1663,Methyl isocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22236,T3D1663,Methyl isocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22237,T3D1663,Methyl isocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22238,T3D1663,Methyl isocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22239,T3D1663,Methyl isocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22240,T3D1663,Methyl isocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22241,T3D1663,Methyl isocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22242,T3D1663,Methyl isocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22243,T3D1663,Methyl isocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22244,T3D1664,Methylene diphenyl diisocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22245,T3D1664,Methylene diphenyl diisocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22246,T3D1664,Methylene diphenyl diisocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22247,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22248,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22249,T3D1664,Methylene diphenyl diisocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22250,T3D1664,Methylene diphenyl diisocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22251,T3D1664,Methylene diphenyl diisocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22252,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22253,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22254,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22255,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22256,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22257,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22258,T3D1664,Methylene diphenyl diisocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22259,T3D1664,Methylene diphenyl diisocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22260,T3D1664,Methylene diphenyl diisocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22261,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22262,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22263,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22264,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22265,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22266,T3D1664,Methylene diphenyl diisocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22267,T3D1664,Methylene diphenyl diisocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22268,T3D1664,Methylene diphenyl diisocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22269,T3D1664,Methylene diphenyl diisocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22270,T3D1664,Methylene diphenyl diisocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22271,T3D1664,Methylene diphenyl diisocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22272,T3D1664,Methylene diphenyl diisocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22273,T3D1664,Methylene diphenyl diisocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22274,T3D1664,Methylene diphenyl diisocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22275,T3D1664,Methylene diphenyl diisocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22276,T3D1664,Methylene diphenyl diisocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22277,T3D1664,Methylene diphenyl diisocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22278,T3D1664,Methylene diphenyl diisocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22279,T3D1664,Methylene diphenyl diisocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22280,T3D1664,Methylene diphenyl diisocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22281,T3D1664,Methylene diphenyl diisocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22282,T3D1664,Methylene diphenyl diisocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22283,T3D1665,Toluene diisocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22284,T3D1665,Toluene diisocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22285,T3D1665,Toluene diisocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22286,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22287,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22288,T3D1665,Toluene diisocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22289,T3D1665,Toluene diisocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22290,T3D1665,Toluene diisocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22291,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22292,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22293,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22294,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22295,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22296,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22297,T3D1665,Toluene diisocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22298,T3D1665,Toluene diisocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22299,T3D1665,Toluene diisocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22300,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22301,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22302,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22303,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22304,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22305,T3D1665,Toluene diisocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22306,T3D1665,Toluene diisocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22307,T3D1665,Toluene diisocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22308,T3D1665,Toluene diisocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22309,T3D1665,Toluene diisocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22310,T3D1665,Toluene diisocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22311,T3D1665,Toluene diisocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22312,T3D1665,Toluene diisocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22313,T3D1665,Toluene diisocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22314,T3D1665,Toluene diisocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22315,T3D1665,Toluene diisocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22316,T3D1665,Toluene diisocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22317,T3D1665,Toluene diisocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22318,T3D1665,Toluene diisocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22319,T3D1665,Toluene diisocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22320,T3D1665,Toluene diisocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22321,T3D1665,Toluene diisocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22322,T3D1666,n-Butyl isocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22323,T3D1666,n-Butyl isocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22324,T3D1666,n-Butyl isocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22325,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22326,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22327,T3D1666,n-Butyl isocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22328,T3D1666,n-Butyl isocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22329,T3D1666,n-Butyl isocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22330,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22331,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22332,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22333,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22334,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22335,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22336,T3D1666,n-Butyl isocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22337,T3D1666,n-Butyl isocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22338,T3D1666,n-Butyl isocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22339,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22340,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22341,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22342,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22343,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22344,T3D1666,n-Butyl isocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22345,T3D1666,n-Butyl isocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22346,T3D1666,n-Butyl isocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22347,T3D1666,n-Butyl isocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22348,T3D1666,n-Butyl isocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22349,T3D1666,n-Butyl isocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22350,T3D1666,n-Butyl isocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22351,T3D1666,n-Butyl isocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22352,T3D1666,n-Butyl isocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22353,T3D1666,n-Butyl isocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22354,T3D1666,n-Butyl isocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22355,T3D1666,n-Butyl isocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22356,T3D1666,n-Butyl isocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22357,T3D1666,n-Butyl isocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22358,T3D1666,n-Butyl isocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22359,T3D1666,n-Butyl isocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22360,T3D1666,n-Butyl isocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22361,T3D1667,"2,4-Toluene diisocyanate","Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22362,T3D1667,"2,4-Toluene diisocyanate","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22363,T3D1667,"2,4-Toluene diisocyanate",Catalase,P04040,Cyanide inhibits catalase. (R211)
22364,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22365,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22366,T3D1667,"2,4-Toluene diisocyanate",Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22367,T3D1667,"2,4-Toluene diisocyanate",Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22368,T3D1667,"2,4-Toluene diisocyanate",Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22369,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22370,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22371,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22372,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22373,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22374,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22375,T3D1667,"2,4-Toluene diisocyanate",Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22376,T3D1667,"2,4-Toluene diisocyanate",Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22377,T3D1667,"2,4-Toluene diisocyanate",Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22378,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22379,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22380,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22381,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22382,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22383,T3D1667,"2,4-Toluene diisocyanate","Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22384,T3D1667,"2,4-Toluene diisocyanate",Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22385,T3D1667,"2,4-Toluene diisocyanate",Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22386,T3D1667,"2,4-Toluene diisocyanate",Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22387,T3D1667,"2,4-Toluene diisocyanate",Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22388,T3D1667,"2,4-Toluene diisocyanate",Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22389,T3D1667,"2,4-Toluene diisocyanate",Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22390,T3D1667,"2,4-Toluene diisocyanate",Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22391,T3D1667,"2,4-Toluene diisocyanate","Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22392,T3D1667,"2,4-Toluene diisocyanate","Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22393,T3D1667,"2,4-Toluene diisocyanate",Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22394,T3D1667,"2,4-Toluene diisocyanate","Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22395,T3D1667,"2,4-Toluene diisocyanate","Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22396,T3D1667,"2,4-Toluene diisocyanate","Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22397,T3D1667,"2,4-Toluene diisocyanate","Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22398,T3D1667,"2,4-Toluene diisocyanate",Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22399,T3D1667,"2,4-Toluene diisocyanate",Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22400,T3D1668,"2,6-Toluene diisocyanate","Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22401,T3D1668,"2,6-Toluene diisocyanate","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22402,T3D1668,"2,6-Toluene diisocyanate",Catalase,P04040,Cyanide inhibits catalase. (R211)
22403,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22404,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22405,T3D1668,"2,6-Toluene diisocyanate",Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22406,T3D1668,"2,6-Toluene diisocyanate",Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22407,T3D1668,"2,6-Toluene diisocyanate",Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22408,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22409,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22410,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22411,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22412,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22413,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22414,T3D1668,"2,6-Toluene diisocyanate",Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22415,T3D1668,"2,6-Toluene diisocyanate",Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22416,T3D1668,"2,6-Toluene diisocyanate",Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22417,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22418,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22419,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22420,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22421,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22422,T3D1668,"2,6-Toluene diisocyanate","Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22423,T3D1668,"2,6-Toluene diisocyanate",Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22424,T3D1668,"2,6-Toluene diisocyanate",Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22425,T3D1668,"2,6-Toluene diisocyanate",Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22426,T3D1668,"2,6-Toluene diisocyanate",Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22427,T3D1668,"2,6-Toluene diisocyanate",Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22428,T3D1668,"2,6-Toluene diisocyanate",Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22429,T3D1668,"2,6-Toluene diisocyanate",Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22430,T3D1668,"2,6-Toluene diisocyanate","Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22431,T3D1668,"2,6-Toluene diisocyanate","Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22432,T3D1668,"2,6-Toluene diisocyanate",Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22433,T3D1668,"2,6-Toluene diisocyanate","Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22434,T3D1668,"2,6-Toluene diisocyanate","Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22435,T3D1668,"2,6-Toluene diisocyanate","Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22436,T3D1668,"2,6-Toluene diisocyanate","Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22437,T3D1668,"2,6-Toluene diisocyanate",Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22438,T3D1668,"2,6-Toluene diisocyanate",Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22439,T3D1669,"3,4-Dichlorophenyl isocyanate","Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22440,T3D1669,"3,4-Dichlorophenyl isocyanate","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22441,T3D1669,"3,4-Dichlorophenyl isocyanate",Catalase,P04040,Cyanide inhibits catalase. (R211)
22442,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22443,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22444,T3D1669,"3,4-Dichlorophenyl isocyanate",Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22445,T3D1669,"3,4-Dichlorophenyl isocyanate",Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22446,T3D1669,"3,4-Dichlorophenyl isocyanate",Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22447,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22448,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22449,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22450,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22451,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22452,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22453,T3D1669,"3,4-Dichlorophenyl isocyanate",Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22454,T3D1669,"3,4-Dichlorophenyl isocyanate",Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22455,T3D1669,"3,4-Dichlorophenyl isocyanate",Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22456,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22457,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22458,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22459,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22460,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22461,T3D1669,"3,4-Dichlorophenyl isocyanate","Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22462,T3D1669,"3,4-Dichlorophenyl isocyanate",Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22463,T3D1669,"3,4-Dichlorophenyl isocyanate",Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22464,T3D1669,"3,4-Dichlorophenyl isocyanate",Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22465,T3D1669,"3,4-Dichlorophenyl isocyanate",Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22466,T3D1669,"3,4-Dichlorophenyl isocyanate",Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22467,T3D1669,"3,4-Dichlorophenyl isocyanate",Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22468,T3D1669,"3,4-Dichlorophenyl isocyanate",Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22469,T3D1669,"3,4-Dichlorophenyl isocyanate","Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22470,T3D1669,"3,4-Dichlorophenyl isocyanate","Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22471,T3D1669,"3,4-Dichlorophenyl isocyanate",Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22472,T3D1669,"3,4-Dichlorophenyl isocyanate","Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22473,T3D1669,"3,4-Dichlorophenyl isocyanate","Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22474,T3D1669,"3,4-Dichlorophenyl isocyanate","Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22475,T3D1669,"3,4-Dichlorophenyl isocyanate","Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22476,T3D1669,"3,4-Dichlorophenyl isocyanate",Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22477,T3D1669,"3,4-Dichlorophenyl isocyanate",Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22478,T3D1670,Methacryloyloxyethyl isocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22479,T3D1670,Methacryloyloxyethyl isocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22480,T3D1670,Methacryloyloxyethyl isocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22481,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22482,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22483,T3D1670,Methacryloyloxyethyl isocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22484,T3D1670,Methacryloyloxyethyl isocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22485,T3D1670,Methacryloyloxyethyl isocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22486,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22487,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22488,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22489,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22490,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22491,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22492,T3D1670,Methacryloyloxyethyl isocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22493,T3D1670,Methacryloyloxyethyl isocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22494,T3D1670,Methacryloyloxyethyl isocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22495,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22496,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22497,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22498,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22499,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22500,T3D1670,Methacryloyloxyethyl isocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22501,T3D1670,Methacryloyloxyethyl isocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22502,T3D1670,Methacryloyloxyethyl isocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22503,T3D1670,Methacryloyloxyethyl isocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22504,T3D1670,Methacryloyloxyethyl isocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22505,T3D1670,Methacryloyloxyethyl isocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22506,T3D1670,Methacryloyloxyethyl isocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22507,T3D1670,Methacryloyloxyethyl isocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22508,T3D1670,Methacryloyloxyethyl isocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22509,T3D1670,Methacryloyloxyethyl isocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22510,T3D1670,Methacryloyloxyethyl isocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22511,T3D1670,Methacryloyloxyethyl isocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22512,T3D1670,Methacryloyloxyethyl isocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22513,T3D1670,Methacryloyloxyethyl isocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22514,T3D1670,Methacryloyloxyethyl isocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22515,T3D1670,Methacryloyloxyethyl isocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22516,T3D1670,Methacryloyloxyethyl isocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22517,T3D1671,Polymethylene polyphenyl isocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22518,T3D1671,Polymethylene polyphenyl isocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22519,T3D1671,Polymethylene polyphenyl isocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22520,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22521,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22522,T3D1671,Polymethylene polyphenyl isocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22523,T3D1671,Polymethylene polyphenyl isocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22524,T3D1671,Polymethylene polyphenyl isocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22525,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22526,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22527,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22528,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22529,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22530,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22531,T3D1671,Polymethylene polyphenyl isocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22532,T3D1671,Polymethylene polyphenyl isocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22533,T3D1671,Polymethylene polyphenyl isocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22534,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22535,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22536,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22537,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22538,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22539,T3D1671,Polymethylene polyphenyl isocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22540,T3D1671,Polymethylene polyphenyl isocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22541,T3D1671,Polymethylene polyphenyl isocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22542,T3D1671,Polymethylene polyphenyl isocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22543,T3D1671,Polymethylene polyphenyl isocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22544,T3D1671,Polymethylene polyphenyl isocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22545,T3D1671,Polymethylene polyphenyl isocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22546,T3D1671,Polymethylene polyphenyl isocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22547,T3D1671,Polymethylene polyphenyl isocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22548,T3D1671,Polymethylene polyphenyl isocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22549,T3D1671,Polymethylene polyphenyl isocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22550,T3D1671,Polymethylene polyphenyl isocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22551,T3D1671,Polymethylene polyphenyl isocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22552,T3D1671,Polymethylene polyphenyl isocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22553,T3D1671,Polymethylene polyphenyl isocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22554,T3D1671,Polymethylene polyphenyl isocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22555,T3D1671,Polymethylene polyphenyl isocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22556,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22557,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22558,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Catalase,P04040,Cyanide inhibits catalase. (R211)
22559,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22560,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22561,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22562,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22563,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22564,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22565,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22566,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22567,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22568,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22569,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22570,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22571,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22572,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22573,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22574,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22575,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22576,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22577,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22578,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22579,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22580,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22581,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22582,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22583,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22584,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22585,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22586,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22587,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22588,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22589,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22590,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22591,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22592,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate","Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22593,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22594,T3D1672,"3,3'-Dimethoxybenzidine-4,4'-diisocyanate",Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22595,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22596,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22597,T3D1673,Methylene bis(4-cyclohexylisocyanate),Catalase,P04040,Cyanide inhibits catalase. (R211)
22598,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22599,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22600,T3D1673,Methylene bis(4-cyclohexylisocyanate),Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22601,T3D1673,Methylene bis(4-cyclohexylisocyanate),Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22602,T3D1673,Methylene bis(4-cyclohexylisocyanate),Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22603,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22604,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22605,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22606,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22607,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22608,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22609,T3D1673,Methylene bis(4-cyclohexylisocyanate),Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22610,T3D1673,Methylene bis(4-cyclohexylisocyanate),Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22611,T3D1673,Methylene bis(4-cyclohexylisocyanate),Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22612,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22613,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22614,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22615,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22616,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22617,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22618,T3D1673,Methylene bis(4-cyclohexylisocyanate),Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22619,T3D1673,Methylene bis(4-cyclohexylisocyanate),Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22620,T3D1673,Methylene bis(4-cyclohexylisocyanate),Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22621,T3D1673,Methylene bis(4-cyclohexylisocyanate),Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22622,T3D1673,Methylene bis(4-cyclohexylisocyanate),Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22623,T3D1673,Methylene bis(4-cyclohexylisocyanate),Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22624,T3D1673,Methylene bis(4-cyclohexylisocyanate),Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22625,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22626,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22627,T3D1673,Methylene bis(4-cyclohexylisocyanate),Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22628,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22629,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22630,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22631,T3D1673,Methylene bis(4-cyclohexylisocyanate),"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22632,T3D1673,Methylene bis(4-cyclohexylisocyanate),Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22633,T3D1673,Methylene bis(4-cyclohexylisocyanate),Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22634,T3D1674,Methyl thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22635,T3D1674,Methyl thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22636,T3D1674,Methyl thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22637,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22638,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22639,T3D1674,Methyl thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22640,T3D1674,Methyl thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22641,T3D1674,Methyl thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22642,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22643,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22644,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22645,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22646,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22647,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22648,T3D1674,Methyl thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22649,T3D1674,Methyl thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22650,T3D1674,Methyl thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22651,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22652,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22653,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22654,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22655,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22656,T3D1674,Methyl thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22657,T3D1674,Methyl thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22658,T3D1674,Methyl thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22659,T3D1674,Methyl thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22660,T3D1674,Methyl thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22661,T3D1674,Methyl thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22662,T3D1674,Methyl thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22663,T3D1674,Methyl thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22664,T3D1674,Methyl thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22665,T3D1674,Methyl thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22666,T3D1674,Methyl thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22667,T3D1674,Methyl thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22668,T3D1674,Methyl thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22669,T3D1674,Methyl thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22670,T3D1674,Methyl thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22671,T3D1674,Methyl thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22672,T3D1674,Methyl thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22673,T3D1675,Ethyl thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22674,T3D1675,Ethyl thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22675,T3D1675,Ethyl thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22676,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22677,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22678,T3D1675,Ethyl thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22679,T3D1675,Ethyl thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22680,T3D1675,Ethyl thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22681,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22682,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22683,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22684,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22685,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22686,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22687,T3D1675,Ethyl thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22688,T3D1675,Ethyl thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22689,T3D1675,Ethyl thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22690,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22691,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22692,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22693,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22694,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22695,T3D1675,Ethyl thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22696,T3D1675,Ethyl thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22697,T3D1675,Ethyl thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22698,T3D1675,Ethyl thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22699,T3D1675,Ethyl thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22700,T3D1675,Ethyl thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22701,T3D1675,Ethyl thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22702,T3D1675,Ethyl thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22703,T3D1675,Ethyl thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22704,T3D1675,Ethyl thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22705,T3D1675,Ethyl thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22706,T3D1675,Ethyl thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22707,T3D1675,Ethyl thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22708,T3D1675,Ethyl thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22709,T3D1675,Ethyl thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22710,T3D1675,Ethyl thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22711,T3D1675,Ethyl thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22712,T3D1676,Methylene thiocyanate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22713,T3D1676,Methylene thiocyanate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22714,T3D1676,Methylene thiocyanate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22715,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22716,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22717,T3D1676,Methylene thiocyanate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22718,T3D1676,Methylene thiocyanate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22719,T3D1676,Methylene thiocyanate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22720,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22721,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22722,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22723,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22724,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22725,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22726,T3D1676,Methylene thiocyanate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22727,T3D1676,Methylene thiocyanate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22728,T3D1676,Methylene thiocyanate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22729,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22730,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22731,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22732,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22733,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22734,T3D1676,Methylene thiocyanate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22735,T3D1676,Methylene thiocyanate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22736,T3D1676,Methylene thiocyanate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22737,T3D1676,Methylene thiocyanate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22738,T3D1676,Methylene thiocyanate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22739,T3D1676,Methylene thiocyanate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22740,T3D1676,Methylene thiocyanate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22741,T3D1676,Methylene thiocyanate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22742,T3D1676,Methylene thiocyanate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22743,T3D1676,Methylene thiocyanate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22744,T3D1676,Methylene thiocyanate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22745,T3D1676,Methylene thiocyanate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22746,T3D1676,Methylene thiocyanate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22747,T3D1676,Methylene thiocyanate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22748,T3D1676,Methylene thiocyanate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22749,T3D1676,Methylene thiocyanate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22750,T3D1676,Methylene thiocyanate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22751,T3D1677,Isobornyl thiocyanoacetate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22752,T3D1677,Isobornyl thiocyanoacetate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22753,T3D1677,Isobornyl thiocyanoacetate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22754,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22755,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22756,T3D1677,Isobornyl thiocyanoacetate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22757,T3D1677,Isobornyl thiocyanoacetate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22758,T3D1677,Isobornyl thiocyanoacetate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22759,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22760,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22761,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22762,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22763,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22764,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22765,T3D1677,Isobornyl thiocyanoacetate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22766,T3D1677,Isobornyl thiocyanoacetate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22767,T3D1677,Isobornyl thiocyanoacetate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22768,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22769,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22770,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22771,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22772,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22773,T3D1677,Isobornyl thiocyanoacetate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22774,T3D1677,Isobornyl thiocyanoacetate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22775,T3D1677,Isobornyl thiocyanoacetate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22776,T3D1677,Isobornyl thiocyanoacetate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22777,T3D1677,Isobornyl thiocyanoacetate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22778,T3D1677,Isobornyl thiocyanoacetate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22779,T3D1677,Isobornyl thiocyanoacetate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22780,T3D1677,Isobornyl thiocyanoacetate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22781,T3D1677,Isobornyl thiocyanoacetate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22782,T3D1677,Isobornyl thiocyanoacetate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22783,T3D1677,Isobornyl thiocyanoacetate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22784,T3D1677,Isobornyl thiocyanoacetate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22785,T3D1677,Isobornyl thiocyanoacetate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22786,T3D1677,Isobornyl thiocyanoacetate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22787,T3D1677,Isobornyl thiocyanoacetate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22788,T3D1677,Isobornyl thiocyanoacetate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22789,T3D1677,Isobornyl thiocyanoacetate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22790,T3D1678,Acetone cyanohydrin,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22791,T3D1678,Acetone cyanohydrin,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22792,T3D1678,Acetone cyanohydrin,Catalase,P04040,Cyanide inhibits catalase. (R211)
22793,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22794,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22795,T3D1678,Acetone cyanohydrin,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22796,T3D1678,Acetone cyanohydrin,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22797,T3D1678,Acetone cyanohydrin,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22798,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22799,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22800,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22801,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22802,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22803,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22804,T3D1678,Acetone cyanohydrin,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22805,T3D1678,Acetone cyanohydrin,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22806,T3D1678,Acetone cyanohydrin,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22807,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22808,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22809,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22810,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22811,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22812,T3D1678,Acetone cyanohydrin,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22813,T3D1678,Acetone cyanohydrin,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22814,T3D1678,Acetone cyanohydrin,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22815,T3D1678,Acetone cyanohydrin,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22816,T3D1678,Acetone cyanohydrin,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22817,T3D1678,Acetone cyanohydrin,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22818,T3D1678,Acetone cyanohydrin,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22819,T3D1678,Acetone cyanohydrin,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22820,T3D1678,Acetone cyanohydrin,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22821,T3D1678,Acetone cyanohydrin,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22822,T3D1678,Acetone cyanohydrin,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22823,T3D1678,Acetone cyanohydrin,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22824,T3D1678,Acetone cyanohydrin,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22825,T3D1678,Acetone cyanohydrin,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22826,T3D1678,Acetone cyanohydrin,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22827,T3D1678,Acetone cyanohydrin,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22828,T3D1678,Acetone cyanohydrin,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22829,T3D1679,Cyanoacetamide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22830,T3D1679,Cyanoacetamide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22831,T3D1679,Cyanoacetamide,Catalase,P04040,Cyanide inhibits catalase. (R211)
22832,T3D1679,Cyanoacetamide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22833,T3D1679,Cyanoacetamide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22834,T3D1679,Cyanoacetamide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22835,T3D1679,Cyanoacetamide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22836,T3D1679,Cyanoacetamide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22837,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22838,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22839,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22840,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22841,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22842,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22843,T3D1679,Cyanoacetamide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22844,T3D1679,Cyanoacetamide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22845,T3D1679,Cyanoacetamide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22846,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22847,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22848,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22849,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22850,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22851,T3D1679,Cyanoacetamide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22852,T3D1679,Cyanoacetamide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22853,T3D1679,Cyanoacetamide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22854,T3D1679,Cyanoacetamide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22855,T3D1679,Cyanoacetamide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22856,T3D1679,Cyanoacetamide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22857,T3D1679,Cyanoacetamide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22858,T3D1679,Cyanoacetamide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22859,T3D1679,Cyanoacetamide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22860,T3D1679,Cyanoacetamide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22861,T3D1679,Cyanoacetamide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22862,T3D1679,Cyanoacetamide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22863,T3D1679,Cyanoacetamide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22864,T3D1679,Cyanoacetamide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22865,T3D1679,Cyanoacetamide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22866,T3D1679,Cyanoacetamide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22867,T3D1679,Cyanoacetamide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22868,T3D1680,Ethyl cyanoacetate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22869,T3D1680,Ethyl cyanoacetate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22870,T3D1680,Ethyl cyanoacetate,Catalase,P04040,Cyanide inhibits catalase. (R211)
22871,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22872,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22873,T3D1680,Ethyl cyanoacetate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22874,T3D1680,Ethyl cyanoacetate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22875,T3D1680,Ethyl cyanoacetate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22876,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22877,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22878,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22879,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22880,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22881,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22882,T3D1680,Ethyl cyanoacetate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22883,T3D1680,Ethyl cyanoacetate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22884,T3D1680,Ethyl cyanoacetate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22885,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22886,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22887,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22888,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22889,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22890,T3D1680,Ethyl cyanoacetate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22891,T3D1680,Ethyl cyanoacetate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22892,T3D1680,Ethyl cyanoacetate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22893,T3D1680,Ethyl cyanoacetate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22894,T3D1680,Ethyl cyanoacetate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22895,T3D1680,Ethyl cyanoacetate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22896,T3D1680,Ethyl cyanoacetate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22897,T3D1680,Ethyl cyanoacetate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22898,T3D1680,Ethyl cyanoacetate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22899,T3D1680,Ethyl cyanoacetate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22900,T3D1680,Ethyl cyanoacetate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22901,T3D1680,Ethyl cyanoacetate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22902,T3D1680,Ethyl cyanoacetate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22903,T3D1680,Ethyl cyanoacetate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22904,T3D1680,Ethyl cyanoacetate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22905,T3D1680,Ethyl cyanoacetate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22906,T3D1680,Ethyl cyanoacetate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22907,T3D1681,"Phenylene-1,4-diisothiocyanate","Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22908,T3D1681,"Phenylene-1,4-diisothiocyanate","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22909,T3D1681,"Phenylene-1,4-diisothiocyanate",Catalase,P04040,Cyanide inhibits catalase. (R211)
22910,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22911,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22912,T3D1681,"Phenylene-1,4-diisothiocyanate",Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22913,T3D1681,"Phenylene-1,4-diisothiocyanate",Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22914,T3D1681,"Phenylene-1,4-diisothiocyanate",Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22915,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22916,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22917,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22918,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22919,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22920,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22921,T3D1681,"Phenylene-1,4-diisothiocyanate",Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22922,T3D1681,"Phenylene-1,4-diisothiocyanate",Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22923,T3D1681,"Phenylene-1,4-diisothiocyanate",Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22924,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22925,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22926,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22927,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22928,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22929,T3D1681,"Phenylene-1,4-diisothiocyanate","Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22930,T3D1681,"Phenylene-1,4-diisothiocyanate",Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22931,T3D1681,"Phenylene-1,4-diisothiocyanate",Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22932,T3D1681,"Phenylene-1,4-diisothiocyanate",Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22933,T3D1681,"Phenylene-1,4-diisothiocyanate",Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22934,T3D1681,"Phenylene-1,4-diisothiocyanate",Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22935,T3D1681,"Phenylene-1,4-diisothiocyanate",Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22936,T3D1681,"Phenylene-1,4-diisothiocyanate",Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22937,T3D1681,"Phenylene-1,4-diisothiocyanate","Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22938,T3D1681,"Phenylene-1,4-diisothiocyanate","Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22939,T3D1681,"Phenylene-1,4-diisothiocyanate",Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22940,T3D1681,"Phenylene-1,4-diisothiocyanate","Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22941,T3D1681,"Phenylene-1,4-diisothiocyanate","Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22942,T3D1681,"Phenylene-1,4-diisothiocyanate","Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22943,T3D1681,"Phenylene-1,4-diisothiocyanate","Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22944,T3D1681,"Phenylene-1,4-diisothiocyanate",Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22945,T3D1681,"Phenylene-1,4-diisothiocyanate",Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22946,T3D1682,Ethylene cyanohydrin,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22947,T3D1682,Ethylene cyanohydrin,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22948,T3D1682,Ethylene cyanohydrin,Catalase,P04040,Cyanide inhibits catalase. (R211)
22949,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22950,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22951,T3D1682,Ethylene cyanohydrin,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22952,T3D1682,Ethylene cyanohydrin,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22953,T3D1682,Ethylene cyanohydrin,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22954,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22955,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22956,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22957,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22958,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22959,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22960,T3D1682,Ethylene cyanohydrin,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22961,T3D1682,Ethylene cyanohydrin,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22962,T3D1682,Ethylene cyanohydrin,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22963,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22964,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22965,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22966,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22967,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22968,T3D1682,Ethylene cyanohydrin,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22969,T3D1682,Ethylene cyanohydrin,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
22970,T3D1682,Ethylene cyanohydrin,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22971,T3D1682,Ethylene cyanohydrin,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
22972,T3D1682,Ethylene cyanohydrin,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
22973,T3D1682,Ethylene cyanohydrin,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
22974,T3D1682,Ethylene cyanohydrin,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
22975,T3D1682,Ethylene cyanohydrin,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
22976,T3D1682,Ethylene cyanohydrin,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
22977,T3D1682,Ethylene cyanohydrin,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
22978,T3D1682,Ethylene cyanohydrin,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
22979,T3D1682,Ethylene cyanohydrin,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
22980,T3D1682,Ethylene cyanohydrin,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
22981,T3D1682,Ethylene cyanohydrin,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
22982,T3D1682,Ethylene cyanohydrin,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
22983,T3D1682,Ethylene cyanohydrin,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
22984,T3D1682,Ethylene cyanohydrin,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
22985,T3D1683,Cyanoacetic acid,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
22986,T3D1683,Cyanoacetic acid,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
22987,T3D1683,Cyanoacetic acid,Catalase,P04040,Cyanide inhibits catalase. (R211)
22988,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22989,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22990,T3D1683,Cyanoacetic acid,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22991,T3D1683,Cyanoacetic acid,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22992,T3D1683,Cyanoacetic acid,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22993,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22994,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22995,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22996,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22997,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22998,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
22999,T3D1683,Cyanoacetic acid,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23000,T3D1683,Cyanoacetic acid,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23001,T3D1683,Cyanoacetic acid,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23002,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23003,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23004,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23005,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23006,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23007,T3D1683,Cyanoacetic acid,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23008,T3D1683,Cyanoacetic acid,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23009,T3D1683,Cyanoacetic acid,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23010,T3D1683,Cyanoacetic acid,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23011,T3D1683,Cyanoacetic acid,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23012,T3D1683,Cyanoacetic acid,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23013,T3D1683,Cyanoacetic acid,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23014,T3D1683,Cyanoacetic acid,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23015,T3D1683,Cyanoacetic acid,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23016,T3D1683,Cyanoacetic acid,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23017,T3D1683,Cyanoacetic acid,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23018,T3D1683,Cyanoacetic acid,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23019,T3D1683,Cyanoacetic acid,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23020,T3D1683,Cyanoacetic acid,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23021,T3D1683,Cyanoacetic acid,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23022,T3D1683,Cyanoacetic acid,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23023,T3D1683,Cyanoacetic acid,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23024,T3D1684,Ferric hexacyanoferrate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23025,T3D1684,Ferric hexacyanoferrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23026,T3D1684,Ferric hexacyanoferrate,Catalase,P04040,Cyanide inhibits catalase. (R211)
23027,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23028,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23029,T3D1684,Ferric hexacyanoferrate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23030,T3D1684,Ferric hexacyanoferrate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23031,T3D1684,Ferric hexacyanoferrate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23032,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23033,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23034,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23035,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23036,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23037,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23038,T3D1684,Ferric hexacyanoferrate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23039,T3D1684,Ferric hexacyanoferrate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23040,T3D1684,Ferric hexacyanoferrate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23041,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23042,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23043,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23044,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23045,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23046,T3D1684,Ferric hexacyanoferrate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23047,T3D1684,Ferric hexacyanoferrate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23048,T3D1684,Ferric hexacyanoferrate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23049,T3D1684,Ferric hexacyanoferrate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23050,T3D1684,Ferric hexacyanoferrate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23051,T3D1684,Ferric hexacyanoferrate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23052,T3D1684,Ferric hexacyanoferrate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23053,T3D1684,Ferric hexacyanoferrate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23054,T3D1684,Ferric hexacyanoferrate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23055,T3D1684,Ferric hexacyanoferrate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23056,T3D1684,Ferric hexacyanoferrate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23057,T3D1684,Ferric hexacyanoferrate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23058,T3D1684,Ferric hexacyanoferrate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23059,T3D1684,Ferric hexacyanoferrate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23060,T3D1684,Ferric hexacyanoferrate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23061,T3D1684,Ferric hexacyanoferrate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23062,T3D1684,Ferric hexacyanoferrate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23063,T3D1685,Acetonitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23064,T3D1685,Acetonitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23065,T3D1685,Acetonitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23066,T3D1685,Acetonitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23067,T3D1685,Acetonitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23068,T3D1685,Acetonitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23069,T3D1685,Acetonitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23070,T3D1685,Acetonitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23071,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23072,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23073,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23074,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23075,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23076,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23077,T3D1685,Acetonitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23078,T3D1685,Acetonitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23079,T3D1685,Acetonitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23080,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23081,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23082,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23083,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23084,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23085,T3D1685,Acetonitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23086,T3D1685,Acetonitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23087,T3D1685,Acetonitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23088,T3D1685,Acetonitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23089,T3D1685,Acetonitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23090,T3D1685,Acetonitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23091,T3D1685,Acetonitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23092,T3D1685,Acetonitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23093,T3D1685,Acetonitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23094,T3D1685,Acetonitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23095,T3D1685,Acetonitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23096,T3D1685,Acetonitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23097,T3D1685,Acetonitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23098,T3D1685,Acetonitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23099,T3D1685,Acetonitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23100,T3D1685,Acetonitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23101,T3D1685,Acetonitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23102,T3D1686,Mandelonitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23103,T3D1686,Mandelonitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23104,T3D1686,Mandelonitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23105,T3D1686,Mandelonitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23106,T3D1686,Mandelonitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23107,T3D1686,Mandelonitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23108,T3D1686,Mandelonitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23109,T3D1686,Mandelonitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23110,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23111,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23112,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23113,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23114,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23115,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23116,T3D1686,Mandelonitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23117,T3D1686,Mandelonitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23118,T3D1686,Mandelonitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23119,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23120,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23121,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23122,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23123,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23124,T3D1686,Mandelonitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23125,T3D1686,Mandelonitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23126,T3D1686,Mandelonitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23127,T3D1686,Mandelonitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23128,T3D1686,Mandelonitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23129,T3D1686,Mandelonitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23130,T3D1686,Mandelonitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23131,T3D1686,Mandelonitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23132,T3D1686,Mandelonitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23133,T3D1686,Mandelonitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23134,T3D1686,Mandelonitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23135,T3D1686,Mandelonitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23136,T3D1686,Mandelonitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23137,T3D1686,Mandelonitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23138,T3D1686,Mandelonitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23139,T3D1686,Mandelonitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23140,T3D1686,Mandelonitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23141,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23142,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23143,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Catalase,P04040,Cyanide inhibits catalase. (R211)
23144,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23145,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23146,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23147,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23148,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23149,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23150,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23151,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23152,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23153,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23154,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23155,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23156,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23157,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23158,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23159,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23160,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23161,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23162,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23163,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23164,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23165,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23166,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23167,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23168,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23169,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23170,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23171,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23172,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23173,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23174,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23175,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23176,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23177,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)","Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23178,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23179,T3D1687,"1,1'-Azobis(cyclohexanecarbonitrile)",Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23180,T3D1688,Acrylonitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23181,T3D1688,Acrylonitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23182,T3D1688,Acrylonitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23183,T3D1688,Acrylonitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23184,T3D1688,Acrylonitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23185,T3D1688,Acrylonitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23186,T3D1688,Acrylonitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23187,T3D1688,Acrylonitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23188,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23189,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23190,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23191,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23192,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23193,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23194,T3D1688,Acrylonitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23195,T3D1688,Acrylonitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23196,T3D1688,Acrylonitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23197,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23198,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23199,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23200,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23201,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23202,T3D1688,Acrylonitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23203,T3D1688,Acrylonitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23204,T3D1688,Acrylonitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23205,T3D1688,Acrylonitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23206,T3D1688,Acrylonitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23207,T3D1688,Acrylonitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23208,T3D1688,Acrylonitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23209,T3D1688,Acrylonitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23210,T3D1688,Acrylonitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23211,T3D1688,Acrylonitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23212,T3D1688,Acrylonitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23213,T3D1688,Acrylonitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23214,T3D1688,Acrylonitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23215,T3D1688,Acrylonitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23216,T3D1688,Acrylonitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23217,T3D1688,Acrylonitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23218,T3D1688,Acrylonitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23219,T3D1689,Adiponitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23220,T3D1689,Adiponitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23221,T3D1689,Adiponitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23222,T3D1689,Adiponitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23223,T3D1689,Adiponitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23224,T3D1689,Adiponitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23225,T3D1689,Adiponitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23226,T3D1689,Adiponitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23227,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23228,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23229,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23230,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23231,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23232,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23233,T3D1689,Adiponitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23234,T3D1689,Adiponitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23235,T3D1689,Adiponitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23236,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23237,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23238,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23239,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23240,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23241,T3D1689,Adiponitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23242,T3D1689,Adiponitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23243,T3D1689,Adiponitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23244,T3D1689,Adiponitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23245,T3D1689,Adiponitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23246,T3D1689,Adiponitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23247,T3D1689,Adiponitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23248,T3D1689,Adiponitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23249,T3D1689,Adiponitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23250,T3D1689,Adiponitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23251,T3D1689,Adiponitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23252,T3D1689,Adiponitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23253,T3D1689,Adiponitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23254,T3D1689,Adiponitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23255,T3D1689,Adiponitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23256,T3D1689,Adiponitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23257,T3D1689,Adiponitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23258,T3D1690,Aminopropionitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23259,T3D1690,Aminopropionitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23260,T3D1690,Aminopropionitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23261,T3D1690,Aminopropionitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23262,T3D1690,Aminopropionitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23263,T3D1690,Aminopropionitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23264,T3D1690,Aminopropionitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23265,T3D1690,Aminopropionitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23266,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23267,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23268,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23269,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23270,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23271,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23272,T3D1690,Aminopropionitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23273,T3D1690,Aminopropionitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23274,T3D1690,Aminopropionitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23275,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23276,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23277,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23278,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23279,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23280,T3D1690,Aminopropionitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23281,T3D1690,Aminopropionitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23282,T3D1690,Aminopropionitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23283,T3D1690,Aminopropionitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23284,T3D1690,Aminopropionitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23285,T3D1690,Aminopropionitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23286,T3D1690,Aminopropionitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23287,T3D1690,Aminopropionitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23288,T3D1690,Aminopropionitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23289,T3D1690,Aminopropionitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23290,T3D1690,Aminopropionitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23291,T3D1690,Aminopropionitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23292,T3D1690,Aminopropionitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23293,T3D1690,Aminopropionitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23294,T3D1690,Aminopropionitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23295,T3D1690,Aminopropionitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23296,T3D1690,Aminopropionitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23297,T3D1691,Benzonitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23298,T3D1691,Benzonitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23299,T3D1691,Benzonitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23300,T3D1691,Benzonitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23301,T3D1691,Benzonitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23302,T3D1691,Benzonitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23303,T3D1691,Benzonitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23304,T3D1691,Benzonitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23305,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23306,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23307,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23308,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23309,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23310,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23311,T3D1691,Benzonitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23312,T3D1691,Benzonitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23313,T3D1691,Benzonitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23314,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23315,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23316,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23317,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23318,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23319,T3D1691,Benzonitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23320,T3D1691,Benzonitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23321,T3D1691,Benzonitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23322,T3D1691,Benzonitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23323,T3D1691,Benzonitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23324,T3D1691,Benzonitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23325,T3D1691,Benzonitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23326,T3D1691,Benzonitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23327,T3D1691,Benzonitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23328,T3D1691,Benzonitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23329,T3D1691,Benzonitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23330,T3D1691,Benzonitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23331,T3D1691,Benzonitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23332,T3D1691,Benzonitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23333,T3D1691,Benzonitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23334,T3D1691,Benzonitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23335,T3D1691,Benzonitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23336,T3D1692,Benzyl cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23337,T3D1692,Benzyl cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23338,T3D1692,Benzyl cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
23339,T3D1692,Benzyl cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23340,T3D1692,Benzyl cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23341,T3D1692,Benzyl cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23342,T3D1692,Benzyl cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23343,T3D1692,Benzyl cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23344,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23345,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23346,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23347,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23348,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23349,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23350,T3D1692,Benzyl cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23351,T3D1692,Benzyl cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23352,T3D1692,Benzyl cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23353,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23354,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23355,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23356,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23357,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23358,T3D1692,Benzyl cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23359,T3D1692,Benzyl cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23360,T3D1692,Benzyl cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23361,T3D1692,Benzyl cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23362,T3D1692,Benzyl cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23363,T3D1692,Benzyl cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23364,T3D1692,Benzyl cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23365,T3D1692,Benzyl cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23366,T3D1692,Benzyl cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23367,T3D1692,Benzyl cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23368,T3D1692,Benzyl cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23369,T3D1692,Benzyl cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23370,T3D1692,Benzyl cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23371,T3D1692,Benzyl cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23372,T3D1692,Benzyl cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23373,T3D1692,Benzyl cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23374,T3D1692,Benzyl cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23375,T3D1693,Bromobenzyl cyanide,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23376,T3D1693,Bromobenzyl cyanide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23377,T3D1693,Bromobenzyl cyanide,Catalase,P04040,Cyanide inhibits catalase. (R211)
23378,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23379,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23380,T3D1693,Bromobenzyl cyanide,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23381,T3D1693,Bromobenzyl cyanide,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23382,T3D1693,Bromobenzyl cyanide,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23383,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23384,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23385,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23386,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23387,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23388,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23389,T3D1693,Bromobenzyl cyanide,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23390,T3D1693,Bromobenzyl cyanide,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23391,T3D1693,Bromobenzyl cyanide,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23392,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23393,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23394,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23395,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23396,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23397,T3D1693,Bromobenzyl cyanide,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23398,T3D1693,Bromobenzyl cyanide,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23399,T3D1693,Bromobenzyl cyanide,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23400,T3D1693,Bromobenzyl cyanide,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23401,T3D1693,Bromobenzyl cyanide,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23402,T3D1693,Bromobenzyl cyanide,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23403,T3D1693,Bromobenzyl cyanide,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23404,T3D1693,Bromobenzyl cyanide,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23405,T3D1693,Bromobenzyl cyanide,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23406,T3D1693,Bromobenzyl cyanide,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23407,T3D1693,Bromobenzyl cyanide,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23408,T3D1693,Bromobenzyl cyanide,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23409,T3D1693,Bromobenzyl cyanide,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23410,T3D1693,Bromobenzyl cyanide,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23411,T3D1693,Bromobenzyl cyanide,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23412,T3D1693,Bromobenzyl cyanide,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23413,T3D1693,Bromobenzyl cyanide,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23414,T3D1694,Bromoxynil,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23415,T3D1694,Bromoxynil,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23416,T3D1694,Bromoxynil,Catalase,P04040,Cyanide inhibits catalase. (R211)
23417,T3D1694,Bromoxynil,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23418,T3D1694,Bromoxynil,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23419,T3D1694,Bromoxynil,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23420,T3D1694,Bromoxynil,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23421,T3D1694,Bromoxynil,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23422,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23423,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23424,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23425,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23426,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23427,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23428,T3D1694,Bromoxynil,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23429,T3D1694,Bromoxynil,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23430,T3D1694,Bromoxynil,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23431,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23432,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23433,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23434,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23435,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23436,T3D1694,Bromoxynil,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23437,T3D1694,Bromoxynil,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23438,T3D1694,Bromoxynil,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23439,T3D1694,Bromoxynil,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23440,T3D1694,Bromoxynil,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23441,T3D1694,Bromoxynil,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23442,T3D1694,Bromoxynil,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23443,T3D1694,Bromoxynil,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23444,T3D1694,Bromoxynil,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23445,T3D1694,Bromoxynil,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23446,T3D1694,Bromoxynil,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23447,T3D1694,Bromoxynil,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23448,T3D1694,Bromoxynil,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23449,T3D1694,Bromoxynil,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23450,T3D1694,Bromoxynil,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23451,T3D1694,Bromoxynil,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23452,T3D1694,Bromoxynil,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23453,T3D1695,Butyl cyanoacrylate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23454,T3D1695,Butyl cyanoacrylate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23455,T3D1695,Butyl cyanoacrylate,Catalase,P04040,Cyanide inhibits catalase. (R211)
23456,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23457,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23458,T3D1695,Butyl cyanoacrylate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23459,T3D1695,Butyl cyanoacrylate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23460,T3D1695,Butyl cyanoacrylate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23461,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23462,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23463,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23464,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23465,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23466,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23467,T3D1695,Butyl cyanoacrylate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23468,T3D1695,Butyl cyanoacrylate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23469,T3D1695,Butyl cyanoacrylate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23470,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23471,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23472,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23473,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23474,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23475,T3D1695,Butyl cyanoacrylate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23476,T3D1695,Butyl cyanoacrylate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23477,T3D1695,Butyl cyanoacrylate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23478,T3D1695,Butyl cyanoacrylate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23479,T3D1695,Butyl cyanoacrylate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23480,T3D1695,Butyl cyanoacrylate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23481,T3D1695,Butyl cyanoacrylate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23482,T3D1695,Butyl cyanoacrylate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23483,T3D1695,Butyl cyanoacrylate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23484,T3D1695,Butyl cyanoacrylate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23485,T3D1695,Butyl cyanoacrylate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23486,T3D1695,Butyl cyanoacrylate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23487,T3D1695,Butyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23488,T3D1695,Butyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23489,T3D1695,Butyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23490,T3D1695,Butyl cyanoacrylate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23491,T3D1695,Butyl cyanoacrylate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23492,T3D1696,Butyronitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23493,T3D1696,Butyronitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23494,T3D1696,Butyronitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23495,T3D1696,Butyronitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23496,T3D1696,Butyronitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23497,T3D1696,Butyronitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23498,T3D1696,Butyronitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23499,T3D1696,Butyronitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23500,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23501,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23502,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23503,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23504,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23505,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23506,T3D1696,Butyronitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23507,T3D1696,Butyronitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23508,T3D1696,Butyronitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23509,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23510,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23511,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23512,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23513,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23514,T3D1696,Butyronitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23515,T3D1696,Butyronitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23516,T3D1696,Butyronitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23517,T3D1696,Butyronitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23518,T3D1696,Butyronitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23519,T3D1696,Butyronitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23520,T3D1696,Butyronitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23521,T3D1696,Butyronitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23522,T3D1696,Butyronitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23523,T3D1696,Butyronitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23524,T3D1696,Butyronitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23525,T3D1696,Butyronitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23526,T3D1696,Butyronitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23527,T3D1696,Butyronitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23528,T3D1696,Butyronitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23529,T3D1696,Butyronitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23530,T3D1696,Butyronitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23531,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23532,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23533,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Catalase,P04040,Cyanide inhibits catalase. (R211)
23534,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23535,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23536,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23537,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23538,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23539,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23540,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23541,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23542,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23543,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23544,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23545,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23546,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23547,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23548,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23549,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23550,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23551,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23552,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23553,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23554,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23555,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23556,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23557,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23558,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23559,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23560,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23561,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23562,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23563,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23564,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23565,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23566,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23567,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23568,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23569,T3D1697,Carbonyl cyanide m-chlorophenyl hydrazone,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23570,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23571,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23572,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Catalase,P04040,Cyanide inhibits catalase. (R211)
23573,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23574,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23575,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23576,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23577,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23578,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23579,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23580,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23581,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23582,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23583,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23584,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23585,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23586,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23587,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23588,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23589,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23590,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23591,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23592,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23593,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23594,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23595,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23596,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23597,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23598,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23599,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23600,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23601,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23602,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23603,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23604,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23605,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23606,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23607,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23608,T3D1698,Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23609,T3D1699,Chlorfenapyr,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23610,T3D1699,Chlorfenapyr,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23611,T3D1699,Chlorfenapyr,Catalase,P04040,Cyanide inhibits catalase. (R211)
23612,T3D1699,Chlorfenapyr,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23613,T3D1699,Chlorfenapyr,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23614,T3D1699,Chlorfenapyr,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23615,T3D1699,Chlorfenapyr,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23616,T3D1699,Chlorfenapyr,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23617,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23618,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23619,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23620,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23621,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23622,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23623,T3D1699,Chlorfenapyr,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23624,T3D1699,Chlorfenapyr,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23625,T3D1699,Chlorfenapyr,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23626,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23627,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23628,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23629,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23630,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23631,T3D1699,Chlorfenapyr,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23632,T3D1699,Chlorfenapyr,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23633,T3D1699,Chlorfenapyr,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23634,T3D1699,Chlorfenapyr,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23635,T3D1699,Chlorfenapyr,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23636,T3D1699,Chlorfenapyr,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23637,T3D1699,Chlorfenapyr,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23638,T3D1699,Chlorfenapyr,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23639,T3D1699,Chlorfenapyr,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23640,T3D1699,Chlorfenapyr,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23641,T3D1699,Chlorfenapyr,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23642,T3D1699,Chlorfenapyr,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23643,T3D1699,Chlorfenapyr,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23644,T3D1699,Chlorfenapyr,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23645,T3D1699,Chlorfenapyr,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23646,T3D1699,Chlorfenapyr,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23647,T3D1699,Chlorfenapyr,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23648,T3D1700,Chlorothalonil,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23649,T3D1700,Chlorothalonil,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23650,T3D1700,Chlorothalonil,Catalase,P04040,Cyanide inhibits catalase. (R211)
23651,T3D1700,Chlorothalonil,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23652,T3D1700,Chlorothalonil,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23653,T3D1700,Chlorothalonil,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23654,T3D1700,Chlorothalonil,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23655,T3D1700,Chlorothalonil,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23656,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23657,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23658,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23659,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23660,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23661,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23662,T3D1700,Chlorothalonil,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23663,T3D1700,Chlorothalonil,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23664,T3D1700,Chlorothalonil,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23665,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23666,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23667,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23668,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23669,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23670,T3D1700,Chlorothalonil,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23671,T3D1700,Chlorothalonil,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23672,T3D1700,Chlorothalonil,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23673,T3D1700,Chlorothalonil,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23674,T3D1700,Chlorothalonil,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23675,T3D1700,Chlorothalonil,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23676,T3D1700,Chlorothalonil,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23677,T3D1700,Chlorothalonil,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23678,T3D1700,Chlorothalonil,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23679,T3D1700,Chlorothalonil,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23680,T3D1700,Chlorothalonil,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23681,T3D1700,Chlorothalonil,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23682,T3D1700,Chlorothalonil,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23683,T3D1700,Chlorothalonil,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23684,T3D1700,Chlorothalonil,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23685,T3D1700,Chlorothalonil,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23686,T3D1700,Chlorothalonil,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23687,T3D1701,"2,6-Dichlorobenzonitrile","Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23688,T3D1701,"2,6-Dichlorobenzonitrile","Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23689,T3D1701,"2,6-Dichlorobenzonitrile",Catalase,P04040,Cyanide inhibits catalase. (R211)
23690,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23691,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23692,T3D1701,"2,6-Dichlorobenzonitrile",Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23693,T3D1701,"2,6-Dichlorobenzonitrile",Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23694,T3D1701,"2,6-Dichlorobenzonitrile",Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23695,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23696,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23697,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23698,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23699,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23700,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23701,T3D1701,"2,6-Dichlorobenzonitrile",Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23702,T3D1701,"2,6-Dichlorobenzonitrile",Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23703,T3D1701,"2,6-Dichlorobenzonitrile",Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23704,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23705,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23706,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23707,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23708,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23709,T3D1701,"2,6-Dichlorobenzonitrile","Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23710,T3D1701,"2,6-Dichlorobenzonitrile",Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23711,T3D1701,"2,6-Dichlorobenzonitrile",Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23712,T3D1701,"2,6-Dichlorobenzonitrile",Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23713,T3D1701,"2,6-Dichlorobenzonitrile",Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23714,T3D1701,"2,6-Dichlorobenzonitrile",Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23715,T3D1701,"2,6-Dichlorobenzonitrile",Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23716,T3D1701,"2,6-Dichlorobenzonitrile",Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23717,T3D1701,"2,6-Dichlorobenzonitrile","Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23718,T3D1701,"2,6-Dichlorobenzonitrile","Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23719,T3D1701,"2,6-Dichlorobenzonitrile",Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23720,T3D1701,"2,6-Dichlorobenzonitrile","Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23721,T3D1701,"2,6-Dichlorobenzonitrile","Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23722,T3D1701,"2,6-Dichlorobenzonitrile","Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23723,T3D1701,"2,6-Dichlorobenzonitrile","Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23724,T3D1701,"2,6-Dichlorobenzonitrile",Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23725,T3D1701,"2,6-Dichlorobenzonitrile",Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23726,T3D1702,Ethyl cyanoacrylate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23727,T3D1702,Ethyl cyanoacrylate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23728,T3D1702,Ethyl cyanoacrylate,Catalase,P04040,Cyanide inhibits catalase. (R211)
23729,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23730,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23731,T3D1702,Ethyl cyanoacrylate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23732,T3D1702,Ethyl cyanoacrylate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23733,T3D1702,Ethyl cyanoacrylate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23734,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23735,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23736,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23737,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23738,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23739,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23740,T3D1702,Ethyl cyanoacrylate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23741,T3D1702,Ethyl cyanoacrylate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23742,T3D1702,Ethyl cyanoacrylate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23743,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23744,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23745,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23746,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23747,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23748,T3D1702,Ethyl cyanoacrylate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23749,T3D1702,Ethyl cyanoacrylate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23750,T3D1702,Ethyl cyanoacrylate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23751,T3D1702,Ethyl cyanoacrylate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23752,T3D1702,Ethyl cyanoacrylate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23753,T3D1702,Ethyl cyanoacrylate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23754,T3D1702,Ethyl cyanoacrylate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23755,T3D1702,Ethyl cyanoacrylate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23756,T3D1702,Ethyl cyanoacrylate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23757,T3D1702,Ethyl cyanoacrylate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23758,T3D1702,Ethyl cyanoacrylate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23759,T3D1702,Ethyl cyanoacrylate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23760,T3D1702,Ethyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23761,T3D1702,Ethyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23762,T3D1702,Ethyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23763,T3D1702,Ethyl cyanoacrylate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23764,T3D1702,Ethyl cyanoacrylate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23765,T3D1037,Fenvalerate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23766,T3D1037,Fenvalerate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23767,T3D1037,Fenvalerate,Catalase,P04040,Cyanide inhibits catalase. (R211)
23768,T3D1037,Fenvalerate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23769,T3D1037,Fenvalerate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23770,T3D1037,Fenvalerate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23771,T3D1037,Fenvalerate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23772,T3D1037,Fenvalerate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23773,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23774,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23775,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23776,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23777,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23778,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23779,T3D1037,Fenvalerate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23780,T3D1037,Fenvalerate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23781,T3D1037,Fenvalerate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23782,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23783,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23784,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23785,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23786,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23787,T3D1037,Fenvalerate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23788,T3D1037,Fenvalerate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23789,T3D1037,Fenvalerate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23790,T3D1037,Fenvalerate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23791,T3D1037,Fenvalerate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23792,T3D1037,Fenvalerate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23793,T3D1037,Fenvalerate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23794,T3D1037,Fenvalerate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23795,T3D1037,Fenvalerate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23796,T3D1037,Fenvalerate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23797,T3D1037,Fenvalerate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23798,T3D1037,Fenvalerate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23799,T3D1037,Fenvalerate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23800,T3D1037,Fenvalerate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23801,T3D1037,Fenvalerate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23802,T3D1037,Fenvalerate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23803,T3D1037,Fenvalerate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23804,T3D1703,Glutaronitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23805,T3D1703,Glutaronitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23806,T3D1703,Glutaronitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23807,T3D1703,Glutaronitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23808,T3D1703,Glutaronitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23809,T3D1703,Glutaronitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23810,T3D1703,Glutaronitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23811,T3D1703,Glutaronitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23812,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23813,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23814,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23815,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23816,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23817,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23818,T3D1703,Glutaronitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23819,T3D1703,Glutaronitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23820,T3D1703,Glutaronitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23821,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23822,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23823,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23824,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23825,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23826,T3D1703,Glutaronitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23827,T3D1703,Glutaronitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23828,T3D1703,Glutaronitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23829,T3D1703,Glutaronitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23830,T3D1703,Glutaronitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23831,T3D1703,Glutaronitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23832,T3D1703,Glutaronitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23833,T3D1703,Glutaronitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23834,T3D1703,Glutaronitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23835,T3D1703,Glutaronitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23836,T3D1703,Glutaronitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23837,T3D1703,Glutaronitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23838,T3D1703,Glutaronitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23839,T3D1703,Glutaronitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23840,T3D1703,Glutaronitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23841,T3D1703,Glutaronitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23842,T3D1703,Glutaronitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23843,T3D1704,Malononitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23844,T3D1704,Malononitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23845,T3D1704,Malononitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23846,T3D1704,Malononitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23847,T3D1704,Malononitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23848,T3D1704,Malononitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23849,T3D1704,Malononitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23850,T3D1704,Malononitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23851,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23852,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23853,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23854,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23855,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23856,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23857,T3D1704,Malononitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23858,T3D1704,Malononitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23859,T3D1704,Malononitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23860,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23861,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23862,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23863,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23864,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23865,T3D1704,Malononitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23866,T3D1704,Malononitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23867,T3D1704,Malononitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23868,T3D1704,Malononitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23869,T3D1704,Malononitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23870,T3D1704,Malononitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23871,T3D1704,Malononitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23872,T3D1704,Malononitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23873,T3D1704,Malononitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23874,T3D1704,Malononitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23875,T3D1704,Malononitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23876,T3D1704,Malononitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23877,T3D1704,Malononitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23878,T3D1704,Malononitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23879,T3D1704,Malononitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23880,T3D1704,Malononitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23881,T3D1704,Malononitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23882,T3D1705,Methyl cyanoacrylate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23883,T3D1705,Methyl cyanoacrylate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23884,T3D1705,Methyl cyanoacrylate,Catalase,P04040,Cyanide inhibits catalase. (R211)
23885,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23886,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23887,T3D1705,Methyl cyanoacrylate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23888,T3D1705,Methyl cyanoacrylate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23889,T3D1705,Methyl cyanoacrylate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23890,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23891,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23892,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23893,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23894,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23895,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23896,T3D1705,Methyl cyanoacrylate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23897,T3D1705,Methyl cyanoacrylate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23898,T3D1705,Methyl cyanoacrylate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23899,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23900,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23901,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23902,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23903,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23904,T3D1705,Methyl cyanoacrylate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23905,T3D1705,Methyl cyanoacrylate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23906,T3D1705,Methyl cyanoacrylate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23907,T3D1705,Methyl cyanoacrylate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23908,T3D1705,Methyl cyanoacrylate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23909,T3D1705,Methyl cyanoacrylate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23910,T3D1705,Methyl cyanoacrylate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23911,T3D1705,Methyl cyanoacrylate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23912,T3D1705,Methyl cyanoacrylate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23913,T3D1705,Methyl cyanoacrylate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23914,T3D1705,Methyl cyanoacrylate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23915,T3D1705,Methyl cyanoacrylate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23916,T3D1705,Methyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23917,T3D1705,Methyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23918,T3D1705,Methyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23919,T3D1705,Methyl cyanoacrylate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23920,T3D1705,Methyl cyanoacrylate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23921,T3D1706,Octyl cyanoacrylate,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23922,T3D1706,Octyl cyanoacrylate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23923,T3D1706,Octyl cyanoacrylate,Catalase,P04040,Cyanide inhibits catalase. (R211)
23924,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23925,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23926,T3D1706,Octyl cyanoacrylate,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23927,T3D1706,Octyl cyanoacrylate,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23928,T3D1706,Octyl cyanoacrylate,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23929,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23930,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23931,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23932,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23933,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23934,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23935,T3D1706,Octyl cyanoacrylate,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23936,T3D1706,Octyl cyanoacrylate,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23937,T3D1706,Octyl cyanoacrylate,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23938,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23939,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23940,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23941,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23942,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23943,T3D1706,Octyl cyanoacrylate,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23944,T3D1706,Octyl cyanoacrylate,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23945,T3D1706,Octyl cyanoacrylate,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23946,T3D1706,Octyl cyanoacrylate,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23947,T3D1706,Octyl cyanoacrylate,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23948,T3D1706,Octyl cyanoacrylate,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23949,T3D1706,Octyl cyanoacrylate,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23950,T3D1706,Octyl cyanoacrylate,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23951,T3D1706,Octyl cyanoacrylate,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23952,T3D1706,Octyl cyanoacrylate,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23953,T3D1706,Octyl cyanoacrylate,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23954,T3D1706,Octyl cyanoacrylate,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23955,T3D1706,Octyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23956,T3D1706,Octyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23957,T3D1706,Octyl cyanoacrylate,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23958,T3D1706,Octyl cyanoacrylate,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23959,T3D1706,Octyl cyanoacrylate,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23960,T3D1707,Phthalonitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
23961,T3D1707,Phthalonitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
23962,T3D1707,Phthalonitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
23963,T3D1707,Phthalonitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23964,T3D1707,Phthalonitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23965,T3D1707,Phthalonitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23966,T3D1707,Phthalonitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23967,T3D1707,Phthalonitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23968,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23969,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23970,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23971,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23972,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23973,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23974,T3D1707,Phthalonitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23975,T3D1707,Phthalonitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23976,T3D1707,Phthalonitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23977,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23978,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23979,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23980,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23981,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23982,T3D1707,Phthalonitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
23983,T3D1707,Phthalonitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
23984,T3D1707,Phthalonitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23985,T3D1707,Phthalonitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
23986,T3D1707,Phthalonitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
23987,T3D1707,Phthalonitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
23988,T3D1707,Phthalonitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
23989,T3D1707,Phthalonitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
23990,T3D1707,Phthalonitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
23991,T3D1707,Phthalonitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
23992,T3D1707,Phthalonitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
23993,T3D1707,Phthalonitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
23994,T3D1707,Phthalonitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
23995,T3D1707,Phthalonitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
23996,T3D1707,Phthalonitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
23997,T3D1707,Phthalonitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
23998,T3D1707,Phthalonitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
23999,T3D1708,Propionitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
24000,T3D1708,Propionitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
24001,T3D1708,Propionitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
24002,T3D1708,Propionitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24003,T3D1708,Propionitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24004,T3D1708,Propionitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24005,T3D1708,Propionitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24006,T3D1708,Propionitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24007,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24008,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24009,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24010,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24011,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24012,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24013,T3D1708,Propionitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24014,T3D1708,Propionitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24015,T3D1708,Propionitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24016,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24017,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24018,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24019,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24020,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24021,T3D1708,Propionitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24022,T3D1708,Propionitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
24023,T3D1708,Propionitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24024,T3D1708,Propionitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
24025,T3D1708,Propionitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
24026,T3D1708,Propionitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
24027,T3D1708,Propionitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
24028,T3D1708,Propionitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
24029,T3D1708,Propionitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
24030,T3D1708,Propionitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
24031,T3D1708,Propionitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
24032,T3D1708,Propionitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
24033,T3D1708,Propionitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
24034,T3D1708,Propionitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
24035,T3D1708,Propionitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
24036,T3D1708,Propionitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24037,T3D1708,Propionitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
24038,T3D1709,Ranelic acid,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
24039,T3D1709,Ranelic acid,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
24040,T3D1709,Ranelic acid,Catalase,P04040,Cyanide inhibits catalase. (R211)
24041,T3D1709,Ranelic acid,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24042,T3D1709,Ranelic acid,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24043,T3D1709,Ranelic acid,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24044,T3D1709,Ranelic acid,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24045,T3D1709,Ranelic acid,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24046,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24047,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24048,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24049,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24050,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24051,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24052,T3D1709,Ranelic acid,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24053,T3D1709,Ranelic acid,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24054,T3D1709,Ranelic acid,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24055,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24056,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24057,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24058,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24059,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24060,T3D1709,Ranelic acid,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24061,T3D1709,Ranelic acid,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
24062,T3D1709,Ranelic acid,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24063,T3D1709,Ranelic acid,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
24064,T3D1709,Ranelic acid,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
24065,T3D1709,Ranelic acid,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
24066,T3D1709,Ranelic acid,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
24067,T3D1709,Ranelic acid,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
24068,T3D1709,Ranelic acid,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
24069,T3D1709,Ranelic acid,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
24070,T3D1709,Ranelic acid,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
24071,T3D1709,Ranelic acid,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
24072,T3D1709,Ranelic acid,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
24073,T3D1709,Ranelic acid,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
24074,T3D1709,Ranelic acid,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
24075,T3D1709,Ranelic acid,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24076,T3D1709,Ranelic acid,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
24077,T3D1710,Succinonitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
24078,T3D1710,Succinonitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
24079,T3D1710,Succinonitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
24080,T3D1710,Succinonitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24081,T3D1710,Succinonitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24082,T3D1710,Succinonitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24083,T3D1710,Succinonitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24084,T3D1710,Succinonitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24085,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24086,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24087,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24088,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24089,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24090,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24091,T3D1710,Succinonitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24092,T3D1710,Succinonitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24093,T3D1710,Succinonitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24094,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24095,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24096,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24097,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24098,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24099,T3D1710,Succinonitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24100,T3D1710,Succinonitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
24101,T3D1710,Succinonitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24102,T3D1710,Succinonitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
24103,T3D1710,Succinonitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
24104,T3D1710,Succinonitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
24105,T3D1710,Succinonitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
24106,T3D1710,Succinonitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
24107,T3D1710,Succinonitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
24108,T3D1710,Succinonitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
24109,T3D1710,Succinonitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
24110,T3D1710,Succinonitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
24111,T3D1710,Succinonitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
24112,T3D1710,Succinonitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
24113,T3D1710,Succinonitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
24114,T3D1710,Succinonitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24115,T3D1710,Succinonitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
24116,T3D1711,Tetracyanoquinodimethane,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
24117,T3D1711,Tetracyanoquinodimethane,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
24118,T3D1711,Tetracyanoquinodimethane,Catalase,P04040,Cyanide inhibits catalase. (R211)
24119,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24120,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24121,T3D1711,Tetracyanoquinodimethane,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24122,T3D1711,Tetracyanoquinodimethane,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24123,T3D1711,Tetracyanoquinodimethane,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24124,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24125,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24126,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24127,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24128,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24129,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24130,T3D1711,Tetracyanoquinodimethane,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24131,T3D1711,Tetracyanoquinodimethane,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24132,T3D1711,Tetracyanoquinodimethane,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24133,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24134,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24135,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24136,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24137,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24138,T3D1711,Tetracyanoquinodimethane,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24139,T3D1711,Tetracyanoquinodimethane,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
24140,T3D1711,Tetracyanoquinodimethane,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24141,T3D1711,Tetracyanoquinodimethane,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
24142,T3D1711,Tetracyanoquinodimethane,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
24143,T3D1711,Tetracyanoquinodimethane,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
24144,T3D1711,Tetracyanoquinodimethane,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
24145,T3D1711,Tetracyanoquinodimethane,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
24146,T3D1711,Tetracyanoquinodimethane,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
24147,T3D1711,Tetracyanoquinodimethane,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
24148,T3D1711,Tetracyanoquinodimethane,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
24149,T3D1711,Tetracyanoquinodimethane,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
24150,T3D1711,Tetracyanoquinodimethane,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
24151,T3D1711,Tetracyanoquinodimethane,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
24152,T3D1711,Tetracyanoquinodimethane,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
24153,T3D1711,Tetracyanoquinodimethane,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24154,T3D1711,Tetracyanoquinodimethane,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
24155,T3D1712,Tetracyanoethylene,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
24156,T3D1712,Tetracyanoethylene,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
24157,T3D1712,Tetracyanoethylene,Catalase,P04040,Cyanide inhibits catalase. (R211)
24158,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24159,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24160,T3D1712,Tetracyanoethylene,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24161,T3D1712,Tetracyanoethylene,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24162,T3D1712,Tetracyanoethylene,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24163,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24164,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24165,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24166,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24167,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24168,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24169,T3D1712,Tetracyanoethylene,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24170,T3D1712,Tetracyanoethylene,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24171,T3D1712,Tetracyanoethylene,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24172,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24173,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24174,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24175,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24176,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24177,T3D1712,Tetracyanoethylene,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24178,T3D1712,Tetracyanoethylene,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
24179,T3D1712,Tetracyanoethylene,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24180,T3D1712,Tetracyanoethylene,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
24181,T3D1712,Tetracyanoethylene,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
24182,T3D1712,Tetracyanoethylene,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
24183,T3D1712,Tetracyanoethylene,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
24184,T3D1712,Tetracyanoethylene,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
24185,T3D1712,Tetracyanoethylene,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
24186,T3D1712,Tetracyanoethylene,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
24187,T3D1712,Tetracyanoethylene,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
24188,T3D1712,Tetracyanoethylene,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
24189,T3D1712,Tetracyanoethylene,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
24190,T3D1712,Tetracyanoethylene,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
24191,T3D1712,Tetracyanoethylene,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
24192,T3D1712,Tetracyanoethylene,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24193,T3D1712,Tetracyanoethylene,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
24194,T3D1713,Tetramethylsuccinonitrile,"Alkaline phosphatase, placental-like",P10696,Cyanide inhibits alkaline phosphatases. (R210)
24195,T3D1713,Tetramethylsuccinonitrile,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,Cyanide inhibits alkaline phosphatases. (R210)
24196,T3D1713,Tetramethylsuccinonitrile,Catalase,P04040,Cyanide inhibits catalase. (R211)
24197,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase polypeptide 7A1, mitochondrial",P24310,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24198,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase polypeptide 7A2, mitochondrial",P14406,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24199,T3D1713,Tetramethylsuccinonitrile,Cytochrome c oxidase subunit 1,P00395,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24200,T3D1713,Tetramethylsuccinonitrile,Cytochrome c oxidase subunit 2,P00403,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24201,T3D1713,Tetramethylsuccinonitrile,Cytochrome c oxidase subunit 3,P00414,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24202,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 4 isoform 1, mitochondrial",P13073,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24203,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 4 isoform 2, mitochondrial",Q96KJ9,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24204,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 5A, mitochondrial",P20674,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24205,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 5B, mitochondrial",P10606,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24206,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 6A1, mitochondrial",P12074,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24207,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 6A2, mitochondrial ",Q02221,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24208,T3D1713,Tetramethylsuccinonitrile,Cytochrome c oxidase subunit 6B1,P14854,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24209,T3D1713,Tetramethylsuccinonitrile,Cytochrome c oxidase subunit 6B2,Q6YFQ2,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24210,T3D1713,Tetramethylsuccinonitrile,Cytochrome c oxidase subunit 6C,P09669,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24211,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 7A3, mitochondrial",O60397,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24212,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 7B, mitochondrial",P24311,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24213,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 7B2, mitochondrial ",Q8TF08,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24214,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 7C, mitochondrial",P15954,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24215,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 8A, mitochondrial",P10176,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24216,T3D1713,Tetramethylsuccinonitrile,"Cytochrome c oxidase subunit 8C, mitochondrial",Q7Z4L0,"Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. (R173)"
24217,T3D1713,Tetramethylsuccinonitrile,Epididymal secretory glutathione peroxidase,O75715,Cyanide inhibits glutathione peroxidases. (R212)
24218,T3D1713,Tetramethylsuccinonitrile,Extracellular superoxide dismutase [Cu-Zn],P08294,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24219,T3D1713,Tetramethylsuccinonitrile,Glutathione peroxidase 1,P07203,Cyanide inhibits glutathione peroxidases. (R212)
24220,T3D1713,Tetramethylsuccinonitrile,Glutathione peroxidase 2,P18283,Cyanide inhibits glutathione peroxidases. (R212)
24221,T3D1713,Tetramethylsuccinonitrile,Glutathione peroxidase 3,P22352,Cyanide inhibits glutathione peroxidases. (R212)
24222,T3D1713,Tetramethylsuccinonitrile,Glutathione peroxidase 6,P59796,Cyanide inhibits glutathione peroxidases. (R212)
24223,T3D1713,Tetramethylsuccinonitrile,Glutathione peroxidase 7,Q96SL4,Cyanide inhibits glutathione peroxidases. (R212)
24224,T3D1713,Tetramethylsuccinonitrile,"Glutathione reductase, mitochondrial",P00390,Cyanide inhibits glutathione reductase. (R213)
24225,T3D1713,Tetramethylsuccinonitrile,"Phospholipid hydroperoxide glutathione peroxidase, mitochondrial",P36969,Cyanide inhibits glutathione peroxidases. (R212)
24226,T3D1713,Tetramethylsuccinonitrile,Probable glutathione peroxidase 8,Q8TED1 ,Cyanide inhibits glutathione peroxidases. (R212)
24227,T3D1713,Tetramethylsuccinonitrile,"Succinate dehydrogenase cytochrome b560 subunit, mitochondrial",Q99643,Cyanide inhibits succinate dehydrogenases. (R213)
24228,T3D1713,Tetramethylsuccinonitrile,"Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial",O14521,Cyanide inhibits succinate dehydrogenases. (R213)
24229,T3D1713,Tetramethylsuccinonitrile,"Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial",P31040,Cyanide inhibits succinate dehydrogenases. (R213)
24230,T3D1713,Tetramethylsuccinonitrile,"Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial",P21912,Cyanide inhibits succinate dehydrogenases. (R213)
24231,T3D1713,Tetramethylsuccinonitrile,Superoxide dismutase [Cu-Zn],P00441,Cyanide inhibits superoxide dismutase [Cu-Zn]. (R209)
24232,T3D1713,Tetramethylsuccinonitrile,Tyrosinase,P14679,Cyanide inhibits tyrosinase. (R214)
24233,T3D0276,Arsenic trisulfide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24234,T3D0276,Arsenic trisulfide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24235,T3D0276,Arsenic trisulfide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24236,T3D0276,Arsenic trisulfide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24237,T3D0276,Arsenic trisulfide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24238,T3D0276,Arsenic trisulfide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24239,T3D0276,Arsenic trisulfide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24240,T3D0276,Arsenic trisulfide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24241,T3D0276,Arsenic trisulfide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24242,T3D0276,Arsenic trisulfide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24243,T3D0276,Arsenic trisulfide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24244,T3D0276,Arsenic trisulfide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24245,T3D0276,Arsenic trisulfide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24246,T3D0276,Arsenic trisulfide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24247,T3D0276,Arsenic trisulfide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24248,T3D0276,Arsenic trisulfide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24249,T3D0276,Arsenic trisulfide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24250,T3D0276,Arsenic trisulfide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24251,T3D0276,Arsenic trisulfide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24252,T3D0276,Arsenic trisulfide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24253,T3D0276,Arsenic trisulfide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24254,T3D0276,Arsenic trisulfide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24255,T3D0276,Arsenic trisulfide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24256,T3D0276,Arsenic trisulfide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24257,T3D0276,Arsenic trisulfide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24258,T3D0276,Arsenic trisulfide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24259,T3D0276,Arsenic trisulfide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24260,T3D0277,Arsenic disulfide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24261,T3D0277,Arsenic disulfide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24262,T3D0277,Arsenic disulfide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24263,T3D0277,Arsenic disulfide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24264,T3D0277,Arsenic disulfide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24265,T3D0277,Arsenic disulfide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24266,T3D0277,Arsenic disulfide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24267,T3D0277,Arsenic disulfide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24268,T3D0277,Arsenic disulfide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24269,T3D0277,Arsenic disulfide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24270,T3D0277,Arsenic disulfide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24271,T3D0277,Arsenic disulfide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24272,T3D0277,Arsenic disulfide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24273,T3D0277,Arsenic disulfide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24274,T3D0277,Arsenic disulfide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24275,T3D0277,Arsenic disulfide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24276,T3D0277,Arsenic disulfide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24277,T3D0277,Arsenic disulfide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24278,T3D0277,Arsenic disulfide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24279,T3D0277,Arsenic disulfide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24280,T3D0277,Arsenic disulfide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24281,T3D0277,Arsenic disulfide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24282,T3D0277,Arsenic disulfide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24283,T3D0277,Arsenic disulfide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24284,T3D0277,Arsenic disulfide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24285,T3D0277,Arsenic disulfide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24286,T3D0277,Arsenic disulfide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24287,T3D0278,Arsenic pentasulfide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24288,T3D0278,Arsenic pentasulfide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24289,T3D0278,Arsenic pentasulfide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24290,T3D0278,Arsenic pentasulfide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24291,T3D0278,Arsenic pentasulfide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24292,T3D0278,Arsenic pentasulfide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24293,T3D0278,Arsenic pentasulfide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24294,T3D0278,Arsenic pentasulfide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24295,T3D0278,Arsenic pentasulfide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24296,T3D0278,Arsenic pentasulfide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24297,T3D0278,Arsenic pentasulfide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24298,T3D0278,Arsenic pentasulfide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24299,T3D0278,Arsenic pentasulfide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24300,T3D0278,Arsenic pentasulfide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24301,T3D0278,Arsenic pentasulfide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24302,T3D0278,Arsenic pentasulfide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24303,T3D0278,Arsenic pentasulfide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24304,T3D0278,Arsenic pentasulfide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24305,T3D0278,Arsenic pentasulfide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24306,T3D0278,Arsenic pentasulfide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24307,T3D0278,Arsenic pentasulfide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24308,T3D0278,Arsenic pentasulfide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24309,T3D0278,Arsenic pentasulfide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24310,T3D0278,Arsenic pentasulfide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24311,T3D0278,Arsenic pentasulfide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24312,T3D0278,Arsenic pentasulfide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24313,T3D0279,Arsenic trichloride,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24314,T3D0279,Arsenic trichloride,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24315,T3D0279,Arsenic trichloride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24316,T3D0279,Arsenic trichloride,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24317,T3D0279,Arsenic trichloride,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24318,T3D0279,Arsenic trichloride,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24319,T3D0279,Arsenic trichloride,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24320,T3D0279,Arsenic trichloride,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24321,T3D0279,Arsenic trichloride,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24322,T3D0279,Arsenic trichloride,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24323,T3D0279,Arsenic trichloride,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24324,T3D0279,Arsenic trichloride,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24325,T3D0279,Arsenic trichloride,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24326,T3D0279,Arsenic trichloride,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24327,T3D0279,Arsenic trichloride,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24328,T3D0279,Arsenic trichloride,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24329,T3D0279,Arsenic trichloride,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24330,T3D0279,Arsenic trichloride,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24331,T3D0279,Arsenic trichloride,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24332,T3D0279,Arsenic trichloride,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24333,T3D0279,Arsenic trichloride,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24334,T3D0279,Arsenic trichloride,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24335,T3D0279,Arsenic trichloride,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24336,T3D0279,Arsenic trichloride,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24337,T3D0279,Arsenic trichloride,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24338,T3D0279,Arsenic trichloride,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24339,T3D0279,Arsenic trichloride,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24340,T3D0282,Arsenous acid,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24341,T3D0282,Arsenous acid,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24342,T3D0282,Arsenous acid,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24343,T3D0282,Arsenous acid,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24344,T3D0282,Arsenous acid,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24345,T3D0282,Arsenous acid,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24346,T3D0282,Arsenous acid,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24347,T3D0282,Arsenous acid,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24348,T3D0282,Arsenous acid,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24349,T3D0282,Arsenous acid,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24350,T3D0282,Arsenous acid,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24351,T3D0282,Arsenous acid,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24352,T3D0282,Arsenous acid,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24353,T3D0282,Arsenous acid,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24354,T3D0282,Arsenous acid,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24355,T3D0282,Arsenous acid,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24356,T3D0282,Arsenous acid,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24357,T3D0282,Arsenous acid,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24358,T3D0282,Arsenous acid,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24359,T3D0282,Arsenous acid,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24360,T3D0282,Arsenous acid,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24361,T3D0282,Arsenous acid,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24362,T3D0282,Arsenous acid,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24363,T3D0282,Arsenous acid,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24364,T3D0282,Arsenous acid,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24365,T3D0282,Arsenous acid,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24366,T3D0283,Arsenenic acid,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24367,T3D0283,Arsenenic acid,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24368,T3D0283,Arsenenic acid,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24369,T3D0283,Arsenenic acid,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24370,T3D0283,Arsenenic acid,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24371,T3D0283,Arsenenic acid,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24372,T3D0283,Arsenenic acid,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24373,T3D0283,Arsenenic acid,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24374,T3D0283,Arsenenic acid,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24375,T3D0283,Arsenenic acid,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24376,T3D0283,Arsenenic acid,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24377,T3D0283,Arsenenic acid,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24378,T3D0283,Arsenenic acid,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24379,T3D0283,Arsenenic acid,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24380,T3D0283,Arsenenic acid,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24381,T3D0283,Arsenenic acid,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24382,T3D0283,Arsenenic acid,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24383,T3D0283,Arsenenic acid,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24384,T3D0283,Arsenenic acid,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24385,T3D0283,Arsenenic acid,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24386,T3D0283,Arsenenic acid,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24387,T3D0283,Arsenenic acid,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24388,T3D0283,Arsenenic acid,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24389,T3D0283,Arsenenic acid,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24390,T3D0283,Arsenenic acid,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24391,T3D0283,Arsenenic acid,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24392,T3D0283,Arsenenic acid,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24393,T3D0285,Ammonium arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24394,T3D0285,Ammonium arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24395,T3D0285,Ammonium arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24396,T3D0285,Ammonium arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24397,T3D0285,Ammonium arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24398,T3D0285,Ammonium arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24399,T3D0285,Ammonium arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24400,T3D0285,Ammonium arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24401,T3D0285,Ammonium arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24402,T3D0285,Ammonium arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24403,T3D0285,Ammonium arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24404,T3D0285,Ammonium arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24405,T3D0285,Ammonium arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24406,T3D0285,Ammonium arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24407,T3D0285,Ammonium arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24408,T3D0285,Ammonium arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24409,T3D0285,Ammonium arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24410,T3D0285,Ammonium arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24411,T3D0285,Ammonium arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24412,T3D0285,Ammonium arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24413,T3D0285,Ammonium arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24414,T3D0285,Ammonium arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24415,T3D0285,Ammonium arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24416,T3D0285,Ammonium arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24417,T3D0285,Ammonium arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24418,T3D0285,Ammonium arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24419,T3D0285,Ammonium arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24420,T3D0286,Copper(II) arsenite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
24421,T3D0286,Copper(II) arsenite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
24422,T3D0286,Copper(II) arsenite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
24423,T3D0286,Copper(II) arsenite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
24424,T3D0286,Copper(II) arsenite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
24425,T3D0286,Copper(II) arsenite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
24426,T3D0286,Copper(II) arsenite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24427,T3D0286,Copper(II) arsenite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
24428,T3D0286,Copper(II) arsenite,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
24429,T3D0286,Copper(II) arsenite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
24430,T3D0286,Copper(II) arsenite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
24431,T3D0286,Copper(II) arsenite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
24432,T3D0286,Copper(II) arsenite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
24433,T3D0286,Copper(II) arsenite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24434,T3D0286,Copper(II) arsenite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24435,T3D0286,Copper(II) arsenite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24436,T3D0286,Copper(II) arsenite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24437,T3D0286,Copper(II) arsenite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24438,T3D0286,Copper(II) arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24439,T3D0286,Copper(II) arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24440,T3D0286,Copper(II) arsenite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24441,T3D0286,Copper(II) arsenite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24442,T3D0286,Copper(II) arsenite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24443,T3D0286,Copper(II) arsenite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24444,T3D0286,Copper(II) arsenite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24445,T3D0286,Copper(II) arsenite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24446,T3D0286,Copper(II) arsenite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24447,T3D0286,Copper(II) arsenite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24448,T3D0286,Copper(II) arsenite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24449,T3D0286,Copper(II) arsenite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24450,T3D0286,Copper(II) arsenite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24451,T3D0286,Copper(II) arsenite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24452,T3D0286,Copper(II) arsenite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24453,T3D0286,Copper(II) arsenite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24454,T3D0286,Copper(II) arsenite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24455,T3D0286,Copper(II) arsenite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24456,T3D0286,Copper(II) arsenite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24457,T3D0286,Copper(II) arsenite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24458,T3D0286,Copper(II) arsenite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24459,T3D0286,Copper(II) arsenite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24460,T3D0286,Copper(II) arsenite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24461,T3D0286,Copper(II) arsenite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24462,T3D0287,Gallium arsenide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24463,T3D0287,Gallium arsenide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24464,T3D0287,Gallium arsenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24465,T3D0287,Gallium arsenide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24466,T3D0287,Gallium arsenide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24467,T3D0287,Gallium arsenide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24468,T3D0287,Gallium arsenide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24469,T3D0287,Gallium arsenide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24470,T3D0287,Gallium arsenide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24471,T3D0287,Gallium arsenide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24472,T3D0287,Gallium arsenide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24473,T3D0287,Gallium arsenide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24474,T3D0287,Gallium arsenide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24475,T3D0287,Gallium arsenide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24476,T3D0287,Gallium arsenide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24477,T3D0287,Gallium arsenide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24478,T3D0287,Gallium arsenide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24479,T3D0287,Gallium arsenide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24480,T3D0287,Gallium arsenide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24481,T3D0287,Gallium arsenide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24482,T3D0287,Gallium arsenide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24483,T3D0287,Gallium arsenide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24484,T3D0287,Gallium arsenide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24485,T3D0287,Gallium arsenide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24486,T3D0287,Gallium arsenide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24487,T3D0287,Gallium arsenide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24488,T3D0287,Gallium arsenide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24489,T3D0288,Copper arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24490,T3D0288,Copper arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24491,T3D0288,Copper arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24492,T3D0288,Copper arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24493,T3D0288,Copper arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24494,T3D0288,Copper arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24495,T3D0288,Copper arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24496,T3D0288,Copper arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24497,T3D0288,Copper arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24498,T3D0288,Copper arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24499,T3D0288,Copper arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24500,T3D0288,Copper arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24501,T3D0288,Copper arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24502,T3D0288,Copper arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24503,T3D0288,Copper arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24504,T3D0288,Copper arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24505,T3D0288,Copper arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24506,T3D0288,Copper arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24507,T3D0288,Copper arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24508,T3D0288,Copper arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24509,T3D0288,Copper arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24510,T3D0288,Copper arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24511,T3D0288,Copper arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24512,T3D0288,Copper arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24513,T3D0288,Copper arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24514,T3D0288,Copper arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24515,T3D0288,Copper arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24516,T3D0289,Copper arsenate hydroxide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24517,T3D0289,Copper arsenate hydroxide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24518,T3D0289,Copper arsenate hydroxide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24519,T3D0289,Copper arsenate hydroxide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24520,T3D0289,Copper arsenate hydroxide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24521,T3D0289,Copper arsenate hydroxide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24522,T3D0289,Copper arsenate hydroxide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24523,T3D0289,Copper arsenate hydroxide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24524,T3D0289,Copper arsenate hydroxide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24525,T3D0289,Copper arsenate hydroxide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24526,T3D0289,Copper arsenate hydroxide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24527,T3D0289,Copper arsenate hydroxide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24528,T3D0289,Copper arsenate hydroxide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24529,T3D0289,Copper arsenate hydroxide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24530,T3D0289,Copper arsenate hydroxide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24531,T3D0289,Copper arsenate hydroxide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24532,T3D0289,Copper arsenate hydroxide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24533,T3D0289,Copper arsenate hydroxide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24534,T3D0289,Copper arsenate hydroxide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24535,T3D0289,Copper arsenate hydroxide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24536,T3D0289,Copper arsenate hydroxide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24537,T3D0289,Copper arsenate hydroxide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24538,T3D0289,Copper arsenate hydroxide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24539,T3D0289,Copper arsenate hydroxide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24540,T3D0289,Copper arsenate hydroxide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24541,T3D0289,Copper arsenate hydroxide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24542,T3D0289,Copper arsenate hydroxide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24543,T3D0290,Potassium arsenite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24544,T3D0290,Potassium arsenite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24545,T3D0290,Potassium arsenite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24546,T3D0290,Potassium arsenite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24547,T3D0290,Potassium arsenite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24548,T3D0290,Potassium arsenite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24549,T3D0290,Potassium arsenite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24550,T3D0290,Potassium arsenite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24551,T3D0290,Potassium arsenite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24552,T3D0290,Potassium arsenite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24553,T3D0290,Potassium arsenite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24554,T3D0290,Potassium arsenite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24555,T3D0290,Potassium arsenite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24556,T3D0290,Potassium arsenite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24557,T3D0290,Potassium arsenite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24558,T3D0290,Potassium arsenite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24559,T3D0290,Potassium arsenite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24560,T3D0290,Potassium arsenite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24561,T3D0290,Potassium arsenite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24562,T3D0290,Potassium arsenite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24563,T3D0290,Potassium arsenite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24564,T3D0290,Potassium arsenite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24565,T3D0290,Potassium arsenite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24566,T3D0290,Potassium arsenite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24567,T3D0290,Potassium arsenite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24568,T3D0290,Potassium arsenite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24569,T3D0290,Potassium arsenite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24570,T3D0292,Arsenic pentoxide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24571,T3D0292,Arsenic pentoxide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24572,T3D0292,Arsenic pentoxide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24573,T3D0292,Arsenic pentoxide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24574,T3D0292,Arsenic pentoxide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24575,T3D0292,Arsenic pentoxide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24576,T3D0292,Arsenic pentoxide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24577,T3D0292,Arsenic pentoxide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24578,T3D0292,Arsenic pentoxide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24579,T3D0292,Arsenic pentoxide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24580,T3D0292,Arsenic pentoxide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24581,T3D0292,Arsenic pentoxide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24582,T3D0292,Arsenic pentoxide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24583,T3D0292,Arsenic pentoxide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24584,T3D0292,Arsenic pentoxide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24585,T3D0292,Arsenic pentoxide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24586,T3D0292,Arsenic pentoxide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24587,T3D0292,Arsenic pentoxide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24588,T3D0292,Arsenic pentoxide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24589,T3D0292,Arsenic pentoxide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24590,T3D0292,Arsenic pentoxide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24591,T3D0292,Arsenic pentoxide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24592,T3D0292,Arsenic pentoxide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24593,T3D0292,Arsenic pentoxide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24594,T3D0292,Arsenic pentoxide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24595,T3D0292,Arsenic pentoxide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24596,T3D0292,Arsenic pentoxide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24597,T3D0293,Magnesium arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24598,T3D0293,Magnesium arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24599,T3D0293,Magnesium arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24600,T3D0293,Magnesium arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24601,T3D0293,Magnesium arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24602,T3D0293,Magnesium arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24603,T3D0293,Magnesium arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24604,T3D0293,Magnesium arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24605,T3D0293,Magnesium arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24606,T3D0293,Magnesium arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24607,T3D0293,Magnesium arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24608,T3D0293,Magnesium arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24609,T3D0293,Magnesium arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24610,T3D0293,Magnesium arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24611,T3D0293,Magnesium arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24612,T3D0293,Magnesium arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24613,T3D0293,Magnesium arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24614,T3D0293,Magnesium arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24615,T3D0293,Magnesium arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24616,T3D0293,Magnesium arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24617,T3D0293,Magnesium arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24618,T3D0293,Magnesium arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24619,T3D0293,Magnesium arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24620,T3D0293,Magnesium arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24621,T3D0293,Magnesium arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24622,T3D0293,Magnesium arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24623,T3D0293,Magnesium arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24624,T3D0294,Manganese arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24625,T3D0294,Manganese arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24626,T3D0294,Manganese arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24627,T3D0294,Manganese arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24628,T3D0294,Manganese arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24629,T3D0294,Manganese arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24630,T3D0294,Manganese arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24631,T3D0294,Manganese arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24632,T3D0294,Manganese arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24633,T3D0294,Manganese arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24634,T3D0294,Manganese arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24635,T3D0294,Manganese arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24636,T3D0294,Manganese arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24637,T3D0294,Manganese arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24638,T3D0294,Manganese arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24639,T3D0294,Manganese arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24640,T3D0294,Manganese arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24641,T3D0294,Manganese arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24642,T3D0294,Manganese arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24643,T3D0294,Manganese arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24644,T3D0294,Manganese arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24645,T3D0294,Manganese arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24646,T3D0294,Manganese arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24647,T3D0294,Manganese arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24648,T3D0294,Manganese arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24649,T3D0294,Manganese arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24650,T3D0294,Manganese arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24651,T3D0296,Lead arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24652,T3D0296,Lead arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24653,T3D0296,Lead arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24654,T3D0296,Lead arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24655,T3D0296,Lead arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24656,T3D0296,Lead arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24657,T3D0296,Lead arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24658,T3D0296,Lead arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24659,T3D0296,Lead arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24660,T3D0296,Lead arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24661,T3D0296,Lead arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24662,T3D0296,Lead arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24663,T3D0296,Lead arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24664,T3D0296,Lead arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24665,T3D0296,Lead arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24666,T3D0296,Lead arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24667,T3D0296,Lead arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24668,T3D0296,Lead arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24669,T3D0296,Lead arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24670,T3D0296,Lead arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24671,T3D0296,Lead arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24672,T3D0296,Lead arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24673,T3D0296,Lead arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24674,T3D0296,Lead arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24675,T3D0296,Lead arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24676,T3D0296,Lead arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24677,T3D0296,Lead arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24678,T3D0297,Potassium arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24679,T3D0297,Potassium arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24680,T3D0297,Potassium arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24681,T3D0297,Potassium arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24682,T3D0297,Potassium arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24683,T3D0297,Potassium arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24684,T3D0297,Potassium arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24685,T3D0297,Potassium arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24686,T3D0297,Potassium arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24687,T3D0297,Potassium arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24688,T3D0297,Potassium arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24689,T3D0297,Potassium arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24690,T3D0297,Potassium arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24691,T3D0297,Potassium arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24692,T3D0297,Potassium arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24693,T3D0297,Potassium arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24694,T3D0297,Potassium arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24695,T3D0297,Potassium arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24696,T3D0297,Potassium arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24697,T3D0297,Potassium arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24698,T3D0297,Potassium arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24699,T3D0297,Potassium arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24700,T3D0297,Potassium arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24701,T3D0297,Potassium arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24702,T3D0297,Potassium arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24703,T3D0297,Potassium arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24704,T3D0297,Potassium arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24705,T3D0298,Sodium arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24706,T3D0298,Sodium arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24707,T3D0298,Sodium arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24708,T3D0298,Sodium arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24709,T3D0298,Sodium arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24710,T3D0298,Sodium arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24711,T3D0298,Sodium arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24712,T3D0298,Sodium arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24713,T3D0298,Sodium arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24714,T3D0298,Sodium arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24715,T3D0298,Sodium arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24716,T3D0298,Sodium arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24717,T3D0298,Sodium arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24718,T3D0298,Sodium arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24719,T3D0298,Sodium arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24720,T3D0298,Sodium arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24721,T3D0298,Sodium arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24722,T3D0298,Sodium arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24723,T3D0298,Sodium arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24724,T3D0298,Sodium arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24725,T3D0298,Sodium arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24726,T3D0298,Sodium arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24727,T3D0298,Sodium arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24728,T3D0298,Sodium arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24729,T3D0298,Sodium arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24730,T3D0298,Sodium arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24731,T3D0298,Sodium arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24732,T3D0299,Zinc arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24733,T3D0299,Zinc arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24734,T3D0299,Zinc arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24735,T3D0299,Zinc arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24736,T3D0299,Zinc arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24737,T3D0299,Zinc arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24738,T3D0299,Zinc arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24739,T3D0299,Zinc arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24740,T3D0299,Zinc arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24741,T3D0299,Zinc arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24742,T3D0299,Zinc arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24743,T3D0299,Zinc arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24744,T3D0299,Zinc arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24745,T3D0299,Zinc arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24746,T3D0299,Zinc arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24747,T3D0299,Zinc arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24748,T3D0299,Zinc arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24749,T3D0299,Zinc arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24750,T3D0299,Zinc arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24751,T3D0299,Zinc arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24752,T3D0299,Zinc arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24753,T3D0299,Zinc arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24754,T3D0299,Zinc arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24755,T3D0299,Zinc arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24756,T3D0299,Zinc arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24757,T3D0299,Zinc arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24758,T3D0299,Zinc arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24759,T3D0301,Arsenobetaine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24760,T3D0301,Arsenobetaine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24761,T3D0301,Arsenobetaine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24762,T3D0301,Arsenobetaine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24763,T3D0301,Arsenobetaine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24764,T3D0301,Arsenobetaine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24765,T3D0301,Arsenobetaine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24766,T3D0301,Arsenobetaine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24767,T3D0301,Arsenobetaine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24768,T3D0301,Arsenobetaine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24769,T3D0301,Arsenobetaine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24770,T3D0301,Arsenobetaine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24771,T3D0301,Arsenobetaine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24772,T3D0301,Arsenobetaine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24773,T3D0301,Arsenobetaine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24774,T3D0301,Arsenobetaine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24775,T3D0301,Arsenobetaine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24776,T3D0301,Arsenobetaine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24777,T3D0301,Arsenobetaine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24778,T3D0301,Arsenobetaine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24779,T3D0301,Arsenobetaine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24780,T3D0301,Arsenobetaine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24781,T3D0301,Arsenobetaine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24782,T3D0301,Arsenobetaine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24783,T3D0301,Arsenobetaine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24784,T3D0301,Arsenobetaine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24785,T3D0301,Arsenobetaine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24786,T3D0302,Arsenocholine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24787,T3D0302,Arsenocholine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24788,T3D0302,Arsenocholine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24789,T3D0302,Arsenocholine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24790,T3D0302,Arsenocholine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24791,T3D0302,Arsenocholine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24792,T3D0302,Arsenocholine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24793,T3D0302,Arsenocholine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24794,T3D0302,Arsenocholine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24795,T3D0302,Arsenocholine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24796,T3D0302,Arsenocholine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24797,T3D0302,Arsenocholine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24798,T3D0302,Arsenocholine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24799,T3D0302,Arsenocholine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24800,T3D0302,Arsenocholine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24801,T3D0302,Arsenocholine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24802,T3D0302,Arsenocholine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24803,T3D0302,Arsenocholine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24804,T3D0302,Arsenocholine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24805,T3D0302,Arsenocholine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24806,T3D0302,Arsenocholine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24807,T3D0302,Arsenocholine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24808,T3D0302,Arsenocholine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24809,T3D0302,Arsenocholine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24810,T3D0302,Arsenocholine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24811,T3D0302,Arsenocholine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24812,T3D0302,Arsenocholine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24813,T3D0303,Methylarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24814,T3D0303,Methylarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24815,T3D0303,Methylarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24816,T3D0303,Methylarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24817,T3D0303,Methylarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24818,T3D0303,Methylarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24819,T3D0303,Methylarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24820,T3D0303,Methylarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24821,T3D0303,Methylarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24822,T3D0303,Methylarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24823,T3D0303,Methylarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24824,T3D0303,Methylarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24825,T3D0303,Methylarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24826,T3D0303,Methylarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24827,T3D0303,Methylarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24828,T3D0303,Methylarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24829,T3D0303,Methylarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24830,T3D0303,Methylarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24831,T3D0303,Methylarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24832,T3D0303,Methylarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24833,T3D0303,Methylarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24834,T3D0303,Methylarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24835,T3D0303,Methylarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24836,T3D0303,Methylarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24837,T3D0303,Methylarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24838,T3D0303,Methylarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24839,T3D0303,Methylarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24840,T3D0304,Dimethylarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24841,T3D0304,Dimethylarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24842,T3D0304,Dimethylarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24843,T3D0304,Dimethylarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24844,T3D0304,Dimethylarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24845,T3D0304,Dimethylarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24846,T3D0304,Dimethylarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24847,T3D0304,Dimethylarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24848,T3D0304,Dimethylarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24849,T3D0304,Dimethylarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24850,T3D0304,Dimethylarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24851,T3D0304,Dimethylarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24852,T3D0304,Dimethylarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24853,T3D0304,Dimethylarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24854,T3D0304,Dimethylarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24855,T3D0304,Dimethylarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24856,T3D0304,Dimethylarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24857,T3D0304,Dimethylarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24858,T3D0304,Dimethylarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24859,T3D0304,Dimethylarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24860,T3D0304,Dimethylarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24861,T3D0304,Dimethylarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24862,T3D0304,Dimethylarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24863,T3D0304,Dimethylarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24864,T3D0304,Dimethylarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24865,T3D0304,Dimethylarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24866,T3D0304,Dimethylarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24867,T3D0305,Trimethylarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24868,T3D0305,Trimethylarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24869,T3D0305,Trimethylarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24870,T3D0305,Trimethylarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24871,T3D0305,Trimethylarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24872,T3D0305,Trimethylarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24873,T3D0305,Trimethylarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24874,T3D0305,Trimethylarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24875,T3D0305,Trimethylarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24876,T3D0305,Trimethylarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24877,T3D0305,Trimethylarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24878,T3D0305,Trimethylarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24879,T3D0305,Trimethylarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24880,T3D0305,Trimethylarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24881,T3D0305,Trimethylarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24882,T3D0305,Trimethylarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24883,T3D0305,Trimethylarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24884,T3D0305,Trimethylarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24885,T3D0305,Trimethylarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24886,T3D0305,Trimethylarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24887,T3D0305,Trimethylarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24888,T3D0305,Trimethylarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24889,T3D0305,Trimethylarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24890,T3D0305,Trimethylarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24891,T3D0305,Trimethylarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24892,T3D0305,Trimethylarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24893,T3D0305,Trimethylarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24894,T3D0307,Methylarsonic acid,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24895,T3D0307,Methylarsonic acid,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24896,T3D0307,Methylarsonic acid,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24897,T3D0307,Methylarsonic acid,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24898,T3D0307,Methylarsonic acid,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24899,T3D0307,Methylarsonic acid,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24900,T3D0307,Methylarsonic acid,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24901,T3D0307,Methylarsonic acid,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24902,T3D0307,Methylarsonic acid,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24903,T3D0307,Methylarsonic acid,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24904,T3D0307,Methylarsonic acid,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24905,T3D0307,Methylarsonic acid,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24906,T3D0307,Methylarsonic acid,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24907,T3D0307,Methylarsonic acid,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24908,T3D0307,Methylarsonic acid,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24909,T3D0307,Methylarsonic acid,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24910,T3D0307,Methylarsonic acid,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24911,T3D0307,Methylarsonic acid,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24912,T3D0307,Methylarsonic acid,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24913,T3D0307,Methylarsonic acid,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24914,T3D0307,Methylarsonic acid,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24915,T3D0307,Methylarsonic acid,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24916,T3D0307,Methylarsonic acid,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24917,T3D0307,Methylarsonic acid,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24918,T3D0307,Methylarsonic acid,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24919,T3D0307,Methylarsonic acid,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24920,T3D0307,Methylarsonic acid,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24921,T3D0308,"Methylarsonic acid, disodium salt",Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24922,T3D0308,"Methylarsonic acid, disodium salt",Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24923,T3D0308,"Methylarsonic acid, disodium salt",Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24924,T3D0308,"Methylarsonic acid, disodium salt",Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24925,T3D0308,"Methylarsonic acid, disodium salt",Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24926,T3D0308,"Methylarsonic acid, disodium salt","Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24927,T3D0308,"Methylarsonic acid, disodium salt","Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24928,T3D0308,"Methylarsonic acid, disodium salt","Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24929,T3D0308,"Methylarsonic acid, disodium salt",Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24930,T3D0308,"Methylarsonic acid, disodium salt",Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24931,T3D0308,"Methylarsonic acid, disodium salt",Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24932,T3D0308,"Methylarsonic acid, disodium salt",Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24933,T3D0308,"Methylarsonic acid, disodium salt",Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24934,T3D0308,"Methylarsonic acid, disodium salt",Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24935,T3D0308,"Methylarsonic acid, disodium salt",Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24936,T3D0308,"Methylarsonic acid, disodium salt",Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24937,T3D0308,"Methylarsonic acid, disodium salt",Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24938,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24939,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24940,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24941,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24942,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24943,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24944,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24945,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24946,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24947,T3D0308,"Methylarsonic acid, disodium salt",Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24948,T3D0309,"Methylarsonic acid, monosodium salt",Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24949,T3D0309,"Methylarsonic acid, monosodium salt",Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24950,T3D0309,"Methylarsonic acid, monosodium salt",Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24951,T3D0309,"Methylarsonic acid, monosodium salt",Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24952,T3D0309,"Methylarsonic acid, monosodium salt",Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24953,T3D0309,"Methylarsonic acid, monosodium salt","Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24954,T3D0309,"Methylarsonic acid, monosodium salt","Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24955,T3D0309,"Methylarsonic acid, monosodium salt","Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24956,T3D0309,"Methylarsonic acid, monosodium salt",Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24957,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24958,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24959,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24960,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24961,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24962,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24963,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24964,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24965,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24966,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24967,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24968,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24969,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24970,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24971,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24972,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24973,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24974,T3D0309,"Methylarsonic acid, monosodium salt",Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24975,T3D0310,Benzenearsonic acid,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
24976,T3D0310,Benzenearsonic acid,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
24977,T3D0310,Benzenearsonic acid,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
24978,T3D0310,Benzenearsonic acid,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
24979,T3D0310,Benzenearsonic acid,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
24980,T3D0310,Benzenearsonic acid,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
24981,T3D0310,Benzenearsonic acid,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24982,T3D0310,Benzenearsonic acid,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
24983,T3D0310,Benzenearsonic acid,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
24984,T3D0310,Benzenearsonic acid,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
24985,T3D0310,Benzenearsonic acid,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24986,T3D0310,Benzenearsonic acid,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
24987,T3D0310,Benzenearsonic acid,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
24988,T3D0310,Benzenearsonic acid,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
24989,T3D0310,Benzenearsonic acid,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
24990,T3D0310,Benzenearsonic acid,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
24991,T3D0310,Benzenearsonic acid,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24992,T3D0310,Benzenearsonic acid,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24993,T3D0310,Benzenearsonic acid,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
24994,T3D0310,Benzenearsonic acid,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24995,T3D0310,Benzenearsonic acid,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24996,T3D0310,Benzenearsonic acid,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24997,T3D0310,Benzenearsonic acid,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
24998,T3D0310,Benzenearsonic acid,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
24999,T3D0310,Benzenearsonic acid,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25000,T3D0310,Benzenearsonic acid,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25001,T3D0310,Benzenearsonic acid,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25002,T3D0310,Benzenearsonic acid,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25003,T3D0310,Benzenearsonic acid,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25004,T3D0310,Benzenearsonic acid,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25005,T3D0310,Benzenearsonic acid,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25006,T3D0310,Benzenearsonic acid,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25007,T3D0310,Benzenearsonic acid,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25008,T3D0310,Benzenearsonic acid,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25009,T3D0310,Benzenearsonic acid,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25010,T3D0310,Benzenearsonic acid,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25011,T3D0310,Benzenearsonic acid,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25012,T3D0310,Benzenearsonic acid,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25013,T3D0310,Benzenearsonic acid,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25014,T3D0310,Benzenearsonic acid,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25015,T3D0310,Benzenearsonic acid,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25016,T3D0310,Benzenearsonic acid,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25017,T3D0310,Benzenearsonic acid,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25018,T3D0310,Benzenearsonic acid,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25019,T3D0318,Trimethylarsine oxide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25020,T3D0318,Trimethylarsine oxide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25021,T3D0318,Trimethylarsine oxide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25022,T3D0318,Trimethylarsine oxide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25023,T3D0318,Trimethylarsine oxide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25024,T3D0318,Trimethylarsine oxide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25025,T3D0318,Trimethylarsine oxide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25026,T3D0318,Trimethylarsine oxide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25027,T3D0318,Trimethylarsine oxide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25028,T3D0318,Trimethylarsine oxide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25029,T3D0318,Trimethylarsine oxide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25030,T3D0318,Trimethylarsine oxide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25031,T3D0318,Trimethylarsine oxide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25032,T3D0318,Trimethylarsine oxide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25033,T3D0318,Trimethylarsine oxide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25034,T3D0318,Trimethylarsine oxide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25035,T3D0318,Trimethylarsine oxide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25036,T3D0318,Trimethylarsine oxide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25037,T3D0318,Trimethylarsine oxide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25038,T3D0318,Trimethylarsine oxide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25039,T3D0318,Trimethylarsine oxide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25040,T3D0318,Trimethylarsine oxide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25041,T3D0318,Trimethylarsine oxide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25042,T3D0318,Trimethylarsine oxide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25043,T3D0318,Trimethylarsine oxide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25044,T3D0318,Trimethylarsine oxide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25045,T3D0318,Trimethylarsine oxide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25046,T3D1185,Chromated copper arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25047,T3D1185,Chromated copper arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25048,T3D1185,Chromated copper arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25049,T3D1185,Chromated copper arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25050,T3D1185,Chromated copper arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25051,T3D1185,Chromated copper arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25052,T3D1185,Chromated copper arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25053,T3D1185,Chromated copper arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25054,T3D1185,Chromated copper arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25055,T3D1185,Chromated copper arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25056,T3D1185,Chromated copper arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25057,T3D1185,Chromated copper arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25058,T3D1185,Chromated copper arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25059,T3D1185,Chromated copper arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25060,T3D1185,Chromated copper arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25061,T3D1185,Chromated copper arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25062,T3D1185,Chromated copper arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25063,T3D1185,Chromated copper arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25064,T3D1185,Chromated copper arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25065,T3D1185,Chromated copper arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25066,T3D1185,Chromated copper arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25067,T3D1185,Chromated copper arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25068,T3D1185,Chromated copper arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25069,T3D1185,Chromated copper arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25070,T3D1185,Chromated copper arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25071,T3D1185,Chromated copper arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25072,T3D1185,Chromated copper arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25073,T3D1185,Chromated copper arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25074,T3D1185,Chromated copper arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25075,T3D1185,Chromated copper arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25076,T3D1185,Chromated copper arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25077,T3D1185,Chromated copper arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25078,T3D1185,Chromated copper arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25079,T3D1185,Chromated copper arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25080,T3D1185,Chromated copper arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25081,T3D1185,Chromated copper arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25082,T3D1185,Chromated copper arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25083,T3D1185,Chromated copper arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25084,T3D1185,Chromated copper arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25085,T3D1185,Chromated copper arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25086,T3D1185,Chromated copper arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25087,T3D1185,Chromated copper arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25088,T3D1185,Chromated copper arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25089,T3D1218,Scheele's Green,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25090,T3D1218,Scheele's Green,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25091,T3D1218,Scheele's Green,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25092,T3D1218,Scheele's Green,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25093,T3D1218,Scheele's Green,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25094,T3D1218,Scheele's Green,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25095,T3D1218,Scheele's Green,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25096,T3D1218,Scheele's Green,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25097,T3D1218,Scheele's Green,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25098,T3D1218,Scheele's Green,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25099,T3D1218,Scheele's Green,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25100,T3D1218,Scheele's Green,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25101,T3D1218,Scheele's Green,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25102,T3D1218,Scheele's Green,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25103,T3D1218,Scheele's Green,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25104,T3D1218,Scheele's Green,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25105,T3D1218,Scheele's Green,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25106,T3D1218,Scheele's Green,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25107,T3D1218,Scheele's Green,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25108,T3D1218,Scheele's Green,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25109,T3D1218,Scheele's Green,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25110,T3D1218,Scheele's Green,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25111,T3D1218,Scheele's Green,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25112,T3D1218,Scheele's Green,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25113,T3D1218,Scheele's Green,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25114,T3D1218,Scheele's Green,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25115,T3D1218,Scheele's Green,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25116,T3D1218,Scheele's Green,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25117,T3D1218,Scheele's Green,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25118,T3D1218,Scheele's Green,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25119,T3D1218,Scheele's Green,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25120,T3D1218,Scheele's Green,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25121,T3D1218,Scheele's Green,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25122,T3D1218,Scheele's Green,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25123,T3D1218,Scheele's Green,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25124,T3D1218,Scheele's Green,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25125,T3D1218,Scheele's Green,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25126,T3D1218,Scheele's Green,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25127,T3D1218,Scheele's Green,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25128,T3D1218,Scheele's Green,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25129,T3D1218,Scheele's Green,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25130,T3D1218,Scheele's Green,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25131,T3D1218,Scheele's Green,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25132,T3D1219,Copper(II) acetoarsenite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25133,T3D1219,Copper(II) acetoarsenite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25134,T3D1219,Copper(II) acetoarsenite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25135,T3D1219,Copper(II) acetoarsenite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25136,T3D1219,Copper(II) acetoarsenite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25137,T3D1219,Copper(II) acetoarsenite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25138,T3D1219,Copper(II) acetoarsenite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25139,T3D1219,Copper(II) acetoarsenite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25140,T3D1219,Copper(II) acetoarsenite,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25141,T3D1219,Copper(II) acetoarsenite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25142,T3D1219,Copper(II) acetoarsenite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25143,T3D1219,Copper(II) acetoarsenite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25144,T3D1219,Copper(II) acetoarsenite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25145,T3D1219,Copper(II) acetoarsenite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25146,T3D1219,Copper(II) acetoarsenite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25147,T3D1219,Copper(II) acetoarsenite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25148,T3D1219,Copper(II) acetoarsenite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25149,T3D1219,Copper(II) acetoarsenite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25150,T3D1219,Copper(II) acetoarsenite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25151,T3D1219,Copper(II) acetoarsenite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25152,T3D1219,Copper(II) acetoarsenite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25153,T3D1219,Copper(II) acetoarsenite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25154,T3D1219,Copper(II) acetoarsenite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25155,T3D1219,Copper(II) acetoarsenite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25156,T3D1219,Copper(II) acetoarsenite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25157,T3D1219,Copper(II) acetoarsenite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25158,T3D1219,Copper(II) acetoarsenite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25159,T3D1219,Copper(II) acetoarsenite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25160,T3D1219,Copper(II) acetoarsenite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25161,T3D1219,Copper(II) acetoarsenite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25162,T3D1219,Copper(II) acetoarsenite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25163,T3D1219,Copper(II) acetoarsenite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25164,T3D1219,Copper(II) acetoarsenite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25165,T3D1219,Copper(II) acetoarsenite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25166,T3D1219,Copper(II) acetoarsenite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25167,T3D1219,Copper(II) acetoarsenite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25168,T3D1219,Copper(II) acetoarsenite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25169,T3D1219,Copper(II) acetoarsenite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25170,T3D1219,Copper(II) acetoarsenite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25171,T3D1219,Copper(II) acetoarsenite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25172,T3D1219,Copper(II) acetoarsenite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25173,T3D1219,Copper(II) acetoarsenite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25174,T3D1219,Copper(II) acetoarsenite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25175,T3D1288,Arsenious acid,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25176,T3D1288,Arsenious acid,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25177,T3D1288,Arsenious acid,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25178,T3D1288,Arsenious acid,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25179,T3D1288,Arsenious acid,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25180,T3D1288,Arsenious acid,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25181,T3D1288,Arsenious acid,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25182,T3D1288,Arsenious acid,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25183,T3D1288,Arsenious acid,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25184,T3D1288,Arsenious acid,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25185,T3D1288,Arsenious acid,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25186,T3D1288,Arsenious acid,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25187,T3D1288,Arsenious acid,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25188,T3D1288,Arsenious acid,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25189,T3D1288,Arsenious acid,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25190,T3D1288,Arsenious acid,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25191,T3D1288,Arsenious acid,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25192,T3D1288,Arsenious acid,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25193,T3D1288,Arsenious acid,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25194,T3D1288,Arsenious acid,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25195,T3D1288,Arsenious acid,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25196,T3D1288,Arsenious acid,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25197,T3D1288,Arsenious acid,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25198,T3D1288,Arsenious acid,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25199,T3D1288,Arsenious acid,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25200,T3D1288,Arsenious acid,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25201,T3D1288,Arsenious acid,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25202,T3D1288,Arsenious acid,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25203,T3D1288,Arsenious acid,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25204,T3D1288,Arsenious acid,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25205,T3D1288,Arsenious acid,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25206,T3D1288,Arsenious acid,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25207,T3D1288,Arsenious acid,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25208,T3D1288,Arsenious acid,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25209,T3D1288,Arsenious acid,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25210,T3D1288,Arsenious acid,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25211,T3D1288,Arsenious acid,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25212,T3D1288,Arsenious acid,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25213,T3D1288,Arsenious acid,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25214,T3D1288,Arsenious acid,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25215,T3D1288,Arsenious acid,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25216,T3D1288,Arsenious acid,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25217,T3D1288,Arsenious acid,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25218,T3D1288,Arsenious acid,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25219,T3D1289,Aluminium arsenide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25220,T3D1289,Aluminium arsenide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25221,T3D1289,Aluminium arsenide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25222,T3D1289,Aluminium arsenide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25223,T3D1289,Aluminium arsenide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25224,T3D1289,Aluminium arsenide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25225,T3D1289,Aluminium arsenide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25226,T3D1289,Aluminium arsenide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25227,T3D1289,Aluminium arsenide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25228,T3D1289,Aluminium arsenide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25229,T3D1289,Aluminium arsenide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25230,T3D1289,Aluminium arsenide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25231,T3D1289,Aluminium arsenide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25232,T3D1289,Aluminium arsenide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25233,T3D1289,Aluminium arsenide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25234,T3D1289,Aluminium arsenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25235,T3D1289,Aluminium arsenide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25236,T3D1289,Aluminium arsenide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25237,T3D1289,Aluminium arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25238,T3D1289,Aluminium arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25239,T3D1289,Aluminium arsenide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25240,T3D1289,Aluminium arsenide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25241,T3D1289,Aluminium arsenide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25242,T3D1289,Aluminium arsenide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25243,T3D1289,Aluminium arsenide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25244,T3D1289,Aluminium arsenide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25245,T3D1289,Aluminium arsenide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25246,T3D1289,Aluminium arsenide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25247,T3D1289,Aluminium arsenide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25248,T3D1289,Aluminium arsenide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25249,T3D1289,Aluminium arsenide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25250,T3D1289,Aluminium arsenide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25251,T3D1289,Aluminium arsenide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25252,T3D1289,Aluminium arsenide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25253,T3D1289,Aluminium arsenide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25254,T3D1289,Aluminium arsenide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25255,T3D1289,Aluminium arsenide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25256,T3D1289,Aluminium arsenide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25257,T3D1289,Aluminium arsenide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25258,T3D1289,Aluminium arsenide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25259,T3D1289,Aluminium arsenide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25260,T3D1289,Aluminium arsenide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25261,T3D1289,Aluminium arsenide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25262,T3D1290,Boron arsenide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25263,T3D1290,Boron arsenide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25264,T3D1290,Boron arsenide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25265,T3D1290,Boron arsenide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25266,T3D1290,Boron arsenide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25267,T3D1290,Boron arsenide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25268,T3D1290,Boron arsenide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25269,T3D1290,Boron arsenide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25270,T3D1290,Boron arsenide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25271,T3D1290,Boron arsenide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25272,T3D1290,Boron arsenide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25273,T3D1290,Boron arsenide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25274,T3D1290,Boron arsenide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25275,T3D1290,Boron arsenide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25276,T3D1290,Boron arsenide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25277,T3D1290,Boron arsenide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25278,T3D1290,Boron arsenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25279,T3D1290,Boron arsenide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25280,T3D1290,Boron arsenide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25281,T3D1290,Boron arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25282,T3D1290,Boron arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25283,T3D1290,Boron arsenide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25284,T3D1290,Boron arsenide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25285,T3D1290,Boron arsenide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25286,T3D1290,Boron arsenide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25287,T3D1290,Boron arsenide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25288,T3D1290,Boron arsenide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25289,T3D1290,Boron arsenide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25290,T3D1290,Boron arsenide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25291,T3D1290,Boron arsenide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25292,T3D1290,Boron arsenide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25293,T3D1290,Boron arsenide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25294,T3D1290,Boron arsenide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25295,T3D1290,Boron arsenide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25296,T3D1290,Boron arsenide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25297,T3D1290,Boron arsenide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25298,T3D1290,Boron arsenide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25299,T3D1290,Boron arsenide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25300,T3D1290,Boron arsenide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25301,T3D1290,Boron arsenide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25302,T3D1290,Boron arsenide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25303,T3D1290,Boron arsenide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25304,T3D1290,Boron arsenide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25305,T3D1290,Boron arsenide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25306,T3D1291,Indium arsenide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25307,T3D1291,Indium arsenide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25308,T3D1291,Indium arsenide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25309,T3D1291,Indium arsenide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25310,T3D1291,Indium arsenide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25311,T3D1291,Indium arsenide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25312,T3D1291,Indium arsenide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25313,T3D1291,Indium arsenide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25314,T3D1291,Indium arsenide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25315,T3D1291,Indium arsenide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25316,T3D1291,Indium arsenide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25317,T3D1291,Indium arsenide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25318,T3D1291,Indium arsenide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25319,T3D1291,Indium arsenide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25320,T3D1291,Indium arsenide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25321,T3D1291,Indium arsenide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25322,T3D1291,Indium arsenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25323,T3D1291,Indium arsenide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25324,T3D1291,Indium arsenide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25325,T3D1291,Indium arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25326,T3D1291,Indium arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25327,T3D1291,Indium arsenide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25328,T3D1291,Indium arsenide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25329,T3D1291,Indium arsenide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25330,T3D1291,Indium arsenide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25331,T3D1291,Indium arsenide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25332,T3D1291,Indium arsenide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25333,T3D1291,Indium arsenide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25334,T3D1291,Indium arsenide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25335,T3D1291,Indium arsenide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25336,T3D1291,Indium arsenide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25337,T3D1291,Indium arsenide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25338,T3D1291,Indium arsenide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25339,T3D1291,Indium arsenide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25340,T3D1291,Indium arsenide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25341,T3D1291,Indium arsenide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25342,T3D1291,Indium arsenide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25343,T3D1291,Indium arsenide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25344,T3D1291,Indium arsenide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25345,T3D1291,Indium arsenide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25346,T3D1291,Indium arsenide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25347,T3D1291,Indium arsenide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25348,T3D1291,Indium arsenide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25349,T3D1291,Indium arsenide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25350,T3D1292,Yttrium(III) arsenide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25351,T3D1292,Yttrium(III) arsenide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25352,T3D1292,Yttrium(III) arsenide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25353,T3D1292,Yttrium(III) arsenide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25354,T3D1292,Yttrium(III) arsenide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25355,T3D1292,Yttrium(III) arsenide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25356,T3D1292,Yttrium(III) arsenide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25357,T3D1292,Yttrium(III) arsenide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25358,T3D1292,Yttrium(III) arsenide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25359,T3D1292,Yttrium(III) arsenide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25360,T3D1292,Yttrium(III) arsenide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25361,T3D1292,Yttrium(III) arsenide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25362,T3D1292,Yttrium(III) arsenide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25363,T3D1292,Yttrium(III) arsenide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25364,T3D1292,Yttrium(III) arsenide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25365,T3D1292,Yttrium(III) arsenide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25366,T3D1292,Yttrium(III) arsenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25367,T3D1292,Yttrium(III) arsenide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25368,T3D1292,Yttrium(III) arsenide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25369,T3D1292,Yttrium(III) arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25370,T3D1292,Yttrium(III) arsenide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25371,T3D1292,Yttrium(III) arsenide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25372,T3D1292,Yttrium(III) arsenide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25373,T3D1292,Yttrium(III) arsenide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25374,T3D1292,Yttrium(III) arsenide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25375,T3D1292,Yttrium(III) arsenide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25376,T3D1292,Yttrium(III) arsenide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25377,T3D1292,Yttrium(III) arsenide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25378,T3D1292,Yttrium(III) arsenide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25379,T3D1292,Yttrium(III) arsenide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25380,T3D1292,Yttrium(III) arsenide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25381,T3D1292,Yttrium(III) arsenide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25382,T3D1292,Yttrium(III) arsenide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25383,T3D1292,Yttrium(III) arsenide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25384,T3D1292,Yttrium(III) arsenide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25385,T3D1292,Yttrium(III) arsenide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25386,T3D1292,Yttrium(III) arsenide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25387,T3D1292,Yttrium(III) arsenide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25388,T3D1292,Yttrium(III) arsenide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25389,T3D1292,Yttrium(III) arsenide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25390,T3D1292,Yttrium(III) arsenide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25391,T3D1292,Yttrium(III) arsenide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25392,T3D1292,Yttrium(III) arsenide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25393,T3D1292,Yttrium(III) arsenide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25394,T3D1293,Acetarsol,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25395,T3D1293,Acetarsol,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25396,T3D1293,Acetarsol,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25397,T3D1293,Acetarsol,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25398,T3D1293,Acetarsol,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25399,T3D1293,Acetarsol,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25400,T3D1293,Acetarsol,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25401,T3D1293,Acetarsol,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25402,T3D1293,Acetarsol,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25403,T3D1293,Acetarsol,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25404,T3D1293,Acetarsol,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25405,T3D1293,Acetarsol,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25406,T3D1293,Acetarsol,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25407,T3D1293,Acetarsol,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25408,T3D1293,Acetarsol,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25409,T3D1293,Acetarsol,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25410,T3D1293,Acetarsol,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25411,T3D1293,Acetarsol,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25412,T3D1293,Acetarsol,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25413,T3D1293,Acetarsol,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25414,T3D1293,Acetarsol,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25415,T3D1293,Acetarsol,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25416,T3D1293,Acetarsol,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25417,T3D1293,Acetarsol,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25418,T3D1293,Acetarsol,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25419,T3D1293,Acetarsol,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25420,T3D1293,Acetarsol,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25421,T3D1293,Acetarsol,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25422,T3D1293,Acetarsol,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25423,T3D1293,Acetarsol,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25424,T3D1293,Acetarsol,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25425,T3D1293,Acetarsol,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25426,T3D1293,Acetarsol,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25427,T3D1293,Acetarsol,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25428,T3D1293,Acetarsol,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25429,T3D1293,Acetarsol,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25430,T3D1293,Acetarsol,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25431,T3D1293,Acetarsol,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25432,T3D1293,Acetarsol,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25433,T3D1293,Acetarsol,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25434,T3D1293,Acetarsol,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25435,T3D1293,Acetarsol,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25436,T3D1293,Acetarsol,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25437,T3D1293,Acetarsol,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25438,T3D1294,Arsabenzene,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25439,T3D1294,Arsabenzene,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25440,T3D1294,Arsabenzene,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25441,T3D1294,Arsabenzene,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25442,T3D1294,Arsabenzene,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25443,T3D1294,Arsabenzene,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25444,T3D1294,Arsabenzene,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25445,T3D1294,Arsabenzene,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25446,T3D1294,Arsabenzene,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25447,T3D1294,Arsabenzene,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25448,T3D1294,Arsabenzene,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25449,T3D1294,Arsabenzene,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25450,T3D1294,Arsabenzene,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25451,T3D1294,Arsabenzene,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25452,T3D1294,Arsabenzene,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25453,T3D1294,Arsabenzene,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25454,T3D1294,Arsabenzene,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25455,T3D1294,Arsabenzene,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25456,T3D1294,Arsabenzene,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25457,T3D1294,Arsabenzene,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25458,T3D1294,Arsabenzene,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25459,T3D1294,Arsabenzene,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25460,T3D1294,Arsabenzene,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25461,T3D1294,Arsabenzene,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25462,T3D1294,Arsabenzene,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25463,T3D1294,Arsabenzene,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25464,T3D1294,Arsabenzene,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25465,T3D1294,Arsabenzene,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25466,T3D1294,Arsabenzene,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25467,T3D1294,Arsabenzene,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25468,T3D1294,Arsabenzene,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25469,T3D1294,Arsabenzene,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25470,T3D1294,Arsabenzene,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25471,T3D1294,Arsabenzene,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25472,T3D1294,Arsabenzene,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25473,T3D1294,Arsabenzene,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25474,T3D1294,Arsabenzene,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25475,T3D1294,Arsabenzene,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25476,T3D1294,Arsabenzene,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25477,T3D1294,Arsabenzene,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25478,T3D1294,Arsabenzene,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25479,T3D1294,Arsabenzene,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25480,T3D1294,Arsabenzene,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25481,T3D1294,Arsabenzene,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25482,T3D1295,Arsenamide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25483,T3D1295,Arsenamide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25484,T3D1295,Arsenamide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25485,T3D1295,Arsenamide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25486,T3D1295,Arsenamide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25487,T3D1295,Arsenamide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25488,T3D1295,Arsenamide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25489,T3D1295,Arsenamide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25490,T3D1295,Arsenamide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25491,T3D1295,Arsenamide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25492,T3D1295,Arsenamide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25493,T3D1295,Arsenamide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25494,T3D1295,Arsenamide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25495,T3D1295,Arsenamide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25496,T3D1295,Arsenamide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25497,T3D1295,Arsenamide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25498,T3D1295,Arsenamide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25499,T3D1295,Arsenamide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25500,T3D1295,Arsenamide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25501,T3D1295,Arsenamide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25502,T3D1295,Arsenamide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25503,T3D1295,Arsenamide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25504,T3D1295,Arsenamide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25505,T3D1295,Arsenamide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25506,T3D1295,Arsenamide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25507,T3D1295,Arsenamide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25508,T3D1295,Arsenamide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25509,T3D1295,Arsenamide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25510,T3D1295,Arsenamide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25511,T3D1295,Arsenamide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25512,T3D1295,Arsenamide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25513,T3D1295,Arsenamide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25514,T3D1295,Arsenamide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25515,T3D1295,Arsenamide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25516,T3D1295,Arsenamide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25517,T3D1295,Arsenamide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25518,T3D1295,Arsenamide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25519,T3D1295,Arsenamide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25520,T3D1295,Arsenamide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25521,T3D1295,Arsenamide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25522,T3D1295,Arsenamide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25523,T3D1295,Arsenamide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25524,T3D1295,Arsenamide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25525,T3D1295,Arsenamide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25526,T3D1296,Arsenic pentachloride,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25527,T3D1296,Arsenic pentachloride,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25528,T3D1296,Arsenic pentachloride,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25529,T3D1296,Arsenic pentachloride,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25530,T3D1296,Arsenic pentachloride,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25531,T3D1296,Arsenic pentachloride,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25532,T3D1296,Arsenic pentachloride,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25533,T3D1296,Arsenic pentachloride,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25534,T3D1296,Arsenic pentachloride,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25535,T3D1296,Arsenic pentachloride,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25536,T3D1296,Arsenic pentachloride,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25537,T3D1296,Arsenic pentachloride,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25538,T3D1296,Arsenic pentachloride,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25539,T3D1296,Arsenic pentachloride,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25540,T3D1296,Arsenic pentachloride,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25541,T3D1296,Arsenic pentachloride,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25542,T3D1296,Arsenic pentachloride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25543,T3D1296,Arsenic pentachloride,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25544,T3D1296,Arsenic pentachloride,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25545,T3D1296,Arsenic pentachloride,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25546,T3D1296,Arsenic pentachloride,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25547,T3D1296,Arsenic pentachloride,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25548,T3D1296,Arsenic pentachloride,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25549,T3D1296,Arsenic pentachloride,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25550,T3D1296,Arsenic pentachloride,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25551,T3D1296,Arsenic pentachloride,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25552,T3D1296,Arsenic pentachloride,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25553,T3D1296,Arsenic pentachloride,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25554,T3D1296,Arsenic pentachloride,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25555,T3D1296,Arsenic pentachloride,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25556,T3D1296,Arsenic pentachloride,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25557,T3D1296,Arsenic pentachloride,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25558,T3D1296,Arsenic pentachloride,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25559,T3D1296,Arsenic pentachloride,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25560,T3D1296,Arsenic pentachloride,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25561,T3D1296,Arsenic pentachloride,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25562,T3D1296,Arsenic pentachloride,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25563,T3D1296,Arsenic pentachloride,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25564,T3D1296,Arsenic pentachloride,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25565,T3D1296,Arsenic pentachloride,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25566,T3D1296,Arsenic pentachloride,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25567,T3D1296,Arsenic pentachloride,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25568,T3D1296,Arsenic pentachloride,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25569,T3D1296,Arsenic pentachloride,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25570,T3D1297,Arsenic pentafluoride,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25571,T3D1297,Arsenic pentafluoride,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25572,T3D1297,Arsenic pentafluoride,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25573,T3D1297,Arsenic pentafluoride,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25574,T3D1297,Arsenic pentafluoride,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25575,T3D1297,Arsenic pentafluoride,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25576,T3D1297,Arsenic pentafluoride,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25577,T3D1297,Arsenic pentafluoride,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25578,T3D1297,Arsenic pentafluoride,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25579,T3D1297,Arsenic pentafluoride,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25580,T3D1297,Arsenic pentafluoride,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25581,T3D1297,Arsenic pentafluoride,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25582,T3D1297,Arsenic pentafluoride,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25583,T3D1297,Arsenic pentafluoride,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25584,T3D1297,Arsenic pentafluoride,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25585,T3D1297,Arsenic pentafluoride,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25586,T3D1297,Arsenic pentafluoride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25587,T3D1297,Arsenic pentafluoride,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25588,T3D1297,Arsenic pentafluoride,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25589,T3D1297,Arsenic pentafluoride,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25590,T3D1297,Arsenic pentafluoride,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25591,T3D1297,Arsenic pentafluoride,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25592,T3D1297,Arsenic pentafluoride,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25593,T3D1297,Arsenic pentafluoride,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25594,T3D1297,Arsenic pentafluoride,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25595,T3D1297,Arsenic pentafluoride,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25596,T3D1297,Arsenic pentafluoride,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25597,T3D1297,Arsenic pentafluoride,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25598,T3D1297,Arsenic pentafluoride,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25599,T3D1297,Arsenic pentafluoride,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25600,T3D1297,Arsenic pentafluoride,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25601,T3D1297,Arsenic pentafluoride,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25602,T3D1297,Arsenic pentafluoride,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25603,T3D1297,Arsenic pentafluoride,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25604,T3D1297,Arsenic pentafluoride,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25605,T3D1297,Arsenic pentafluoride,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25606,T3D1297,Arsenic pentafluoride,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25607,T3D1297,Arsenic pentafluoride,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25608,T3D1297,Arsenic pentafluoride,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25609,T3D1297,Arsenic pentafluoride,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25610,T3D1297,Arsenic pentafluoride,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25611,T3D1297,Arsenic pentafluoride,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25612,T3D1297,Arsenic pentafluoride,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25613,T3D1297,Arsenic pentafluoride,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25614,T3D1298,Arsenic tribromide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25615,T3D1298,Arsenic tribromide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25616,T3D1298,Arsenic tribromide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25617,T3D1298,Arsenic tribromide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25618,T3D1298,Arsenic tribromide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25619,T3D1298,Arsenic tribromide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25620,T3D1298,Arsenic tribromide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25621,T3D1298,Arsenic tribromide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25622,T3D1298,Arsenic tribromide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25623,T3D1298,Arsenic tribromide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25624,T3D1298,Arsenic tribromide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25625,T3D1298,Arsenic tribromide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25626,T3D1298,Arsenic tribromide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25627,T3D1298,Arsenic tribromide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25628,T3D1298,Arsenic tribromide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25629,T3D1298,Arsenic tribromide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25630,T3D1298,Arsenic tribromide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25631,T3D1298,Arsenic tribromide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25632,T3D1298,Arsenic tribromide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25633,T3D1298,Arsenic tribromide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25634,T3D1298,Arsenic tribromide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25635,T3D1298,Arsenic tribromide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25636,T3D1298,Arsenic tribromide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25637,T3D1298,Arsenic tribromide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25638,T3D1298,Arsenic tribromide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25639,T3D1298,Arsenic tribromide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25640,T3D1298,Arsenic tribromide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25641,T3D1298,Arsenic tribromide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25642,T3D1298,Arsenic tribromide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25643,T3D1298,Arsenic tribromide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25644,T3D1298,Arsenic tribromide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25645,T3D1298,Arsenic tribromide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25646,T3D1298,Arsenic tribromide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25647,T3D1298,Arsenic tribromide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25648,T3D1298,Arsenic tribromide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25649,T3D1298,Arsenic tribromide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25650,T3D1298,Arsenic tribromide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25651,T3D1298,Arsenic tribromide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25652,T3D1298,Arsenic tribromide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25653,T3D1298,Arsenic tribromide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25654,T3D1298,Arsenic tribromide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25655,T3D1298,Arsenic tribromide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25656,T3D1298,Arsenic tribromide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25657,T3D1298,Arsenic tribromide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25658,T3D1299,Arsenic trifluoride,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25659,T3D1299,Arsenic trifluoride,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25660,T3D1299,Arsenic trifluoride,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25661,T3D1299,Arsenic trifluoride,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25662,T3D1299,Arsenic trifluoride,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25663,T3D1299,Arsenic trifluoride,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25664,T3D1299,Arsenic trifluoride,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25665,T3D1299,Arsenic trifluoride,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25666,T3D1299,Arsenic trifluoride,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25667,T3D1299,Arsenic trifluoride,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25668,T3D1299,Arsenic trifluoride,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25669,T3D1299,Arsenic trifluoride,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25670,T3D1299,Arsenic trifluoride,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25671,T3D1299,Arsenic trifluoride,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25672,T3D1299,Arsenic trifluoride,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25673,T3D1299,Arsenic trifluoride,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25674,T3D1299,Arsenic trifluoride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25675,T3D1299,Arsenic trifluoride,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25676,T3D1299,Arsenic trifluoride,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25677,T3D1299,Arsenic trifluoride,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25678,T3D1299,Arsenic trifluoride,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25679,T3D1299,Arsenic trifluoride,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25680,T3D1299,Arsenic trifluoride,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25681,T3D1299,Arsenic trifluoride,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25682,T3D1299,Arsenic trifluoride,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25683,T3D1299,Arsenic trifluoride,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25684,T3D1299,Arsenic trifluoride,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25685,T3D1299,Arsenic trifluoride,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25686,T3D1299,Arsenic trifluoride,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25687,T3D1299,Arsenic trifluoride,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25688,T3D1299,Arsenic trifluoride,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25689,T3D1299,Arsenic trifluoride,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25690,T3D1299,Arsenic trifluoride,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25691,T3D1299,Arsenic trifluoride,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25692,T3D1299,Arsenic trifluoride,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25693,T3D1299,Arsenic trifluoride,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25694,T3D1299,Arsenic trifluoride,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25695,T3D1299,Arsenic trifluoride,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25696,T3D1299,Arsenic trifluoride,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25697,T3D1299,Arsenic trifluoride,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25698,T3D1299,Arsenic trifluoride,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25699,T3D1299,Arsenic trifluoride,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25700,T3D1299,Arsenic trifluoride,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25701,T3D1299,Arsenic trifluoride,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25702,T3D1300,Arsenic triiodide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25703,T3D1300,Arsenic triiodide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25704,T3D1300,Arsenic triiodide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25705,T3D1300,Arsenic triiodide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25706,T3D1300,Arsenic triiodide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25707,T3D1300,Arsenic triiodide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25708,T3D1300,Arsenic triiodide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25709,T3D1300,Arsenic triiodide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25710,T3D1300,Arsenic triiodide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25711,T3D1300,Arsenic triiodide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25712,T3D1300,Arsenic triiodide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25713,T3D1300,Arsenic triiodide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25714,T3D1300,Arsenic triiodide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25715,T3D1300,Arsenic triiodide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25716,T3D1300,Arsenic triiodide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25717,T3D1300,Arsenic triiodide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25718,T3D1300,Arsenic triiodide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25719,T3D1300,Arsenic triiodide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25720,T3D1300,Arsenic triiodide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25721,T3D1300,Arsenic triiodide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25722,T3D1300,Arsenic triiodide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25723,T3D1300,Arsenic triiodide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25724,T3D1300,Arsenic triiodide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25725,T3D1300,Arsenic triiodide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25726,T3D1300,Arsenic triiodide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25727,T3D1300,Arsenic triiodide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25728,T3D1300,Arsenic triiodide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25729,T3D1300,Arsenic triiodide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25730,T3D1300,Arsenic triiodide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25731,T3D1300,Arsenic triiodide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25732,T3D1300,Arsenic triiodide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25733,T3D1300,Arsenic triiodide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25734,T3D1300,Arsenic triiodide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25735,T3D1300,Arsenic triiodide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25736,T3D1300,Arsenic triiodide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25737,T3D1300,Arsenic triiodide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25738,T3D1300,Arsenic triiodide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25739,T3D1300,Arsenic triiodide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25740,T3D1300,Arsenic triiodide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25741,T3D1300,Arsenic triiodide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25742,T3D1300,Arsenic triiodide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25743,T3D1300,Arsenic triiodide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25744,T3D1300,Arsenic triiodide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25745,T3D1300,Arsenic triiodide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25746,T3D1301,Arsenic triselenide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25747,T3D1301,Arsenic triselenide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25748,T3D1301,Arsenic triselenide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25749,T3D1301,Arsenic triselenide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25750,T3D1301,Arsenic triselenide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25751,T3D1301,Arsenic triselenide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25752,T3D1301,Arsenic triselenide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25753,T3D1301,Arsenic triselenide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25754,T3D1301,Arsenic triselenide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25755,T3D1301,Arsenic triselenide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25756,T3D1301,Arsenic triselenide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25757,T3D1301,Arsenic triselenide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25758,T3D1301,Arsenic triselenide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25759,T3D1301,Arsenic triselenide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25760,T3D1301,Arsenic triselenide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25761,T3D1301,Arsenic triselenide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25762,T3D1301,Arsenic triselenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25763,T3D1301,Arsenic triselenide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25764,T3D1301,Arsenic triselenide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25765,T3D1301,Arsenic triselenide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25766,T3D1301,Arsenic triselenide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25767,T3D1301,Arsenic triselenide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25768,T3D1301,Arsenic triselenide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25769,T3D1301,Arsenic triselenide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25770,T3D1301,Arsenic triselenide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25771,T3D1301,Arsenic triselenide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25772,T3D1301,Arsenic triselenide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25773,T3D1301,Arsenic triselenide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25774,T3D1301,Arsenic triselenide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25775,T3D1301,Arsenic triselenide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25776,T3D1301,Arsenic triselenide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25777,T3D1301,Arsenic triselenide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25778,T3D1301,Arsenic triselenide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25779,T3D1301,Arsenic triselenide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25780,T3D1301,Arsenic triselenide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25781,T3D1301,Arsenic triselenide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25782,T3D1301,Arsenic triselenide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25783,T3D1301,Arsenic triselenide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25784,T3D1301,Arsenic triselenide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25785,T3D1301,Arsenic triselenide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25786,T3D1301,Arsenic triselenide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25787,T3D1301,Arsenic triselenide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25788,T3D1301,Arsenic triselenide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25789,T3D1301,Arsenic triselenide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25790,T3D1302,Arsole,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25791,T3D1302,Arsole,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25792,T3D1302,Arsole,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25793,T3D1302,Arsole,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25794,T3D1302,Arsole,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25795,T3D1302,Arsole,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25796,T3D1302,Arsole,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25797,T3D1302,Arsole,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25798,T3D1302,Arsole,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25799,T3D1302,Arsole,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25800,T3D1302,Arsole,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25801,T3D1302,Arsole,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25802,T3D1302,Arsole,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25803,T3D1302,Arsole,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25804,T3D1302,Arsole,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25805,T3D1302,Arsole,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25806,T3D1302,Arsole,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25807,T3D1302,Arsole,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25808,T3D1302,Arsole,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25809,T3D1302,Arsole,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25810,T3D1302,Arsole,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25811,T3D1302,Arsole,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25812,T3D1302,Arsole,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25813,T3D1302,Arsole,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25814,T3D1302,Arsole,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25815,T3D1302,Arsole,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25816,T3D1302,Arsole,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25817,T3D1302,Arsole,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25818,T3D1302,Arsole,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25819,T3D1302,Arsole,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25820,T3D1302,Arsole,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25821,T3D1302,Arsole,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25822,T3D1302,Arsole,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25823,T3D1302,Arsole,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25824,T3D1302,Arsole,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25825,T3D1302,Arsole,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25826,T3D1302,Arsole,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25827,T3D1302,Arsole,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25828,T3D1302,Arsole,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25829,T3D1302,Arsole,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25830,T3D1302,Arsole,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25831,T3D1302,Arsole,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25832,T3D1302,Arsole,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25833,T3D1302,Arsole,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25834,T3D1303,p-Azobenzenearsonate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25835,T3D1303,p-Azobenzenearsonate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25836,T3D1303,p-Azobenzenearsonate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25837,T3D1303,p-Azobenzenearsonate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25838,T3D1303,p-Azobenzenearsonate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25839,T3D1303,p-Azobenzenearsonate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25840,T3D1303,p-Azobenzenearsonate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25841,T3D1303,p-Azobenzenearsonate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25842,T3D1303,p-Azobenzenearsonate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25843,T3D1303,p-Azobenzenearsonate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25844,T3D1303,p-Azobenzenearsonate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25845,T3D1303,p-Azobenzenearsonate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25846,T3D1303,p-Azobenzenearsonate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25847,T3D1303,p-Azobenzenearsonate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25848,T3D1303,p-Azobenzenearsonate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25849,T3D1303,p-Azobenzenearsonate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25850,T3D1303,p-Azobenzenearsonate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25851,T3D1303,p-Azobenzenearsonate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25852,T3D1303,p-Azobenzenearsonate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25853,T3D1303,p-Azobenzenearsonate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25854,T3D1303,p-Azobenzenearsonate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25855,T3D1303,p-Azobenzenearsonate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25856,T3D1303,p-Azobenzenearsonate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25857,T3D1303,p-Azobenzenearsonate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25858,T3D1303,p-Azobenzenearsonate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25859,T3D1303,p-Azobenzenearsonate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25860,T3D1303,p-Azobenzenearsonate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25861,T3D1303,p-Azobenzenearsonate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25862,T3D1303,p-Azobenzenearsonate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25863,T3D1303,p-Azobenzenearsonate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25864,T3D1303,p-Azobenzenearsonate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25865,T3D1303,p-Azobenzenearsonate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25866,T3D1303,p-Azobenzenearsonate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25867,T3D1303,p-Azobenzenearsonate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25868,T3D1303,p-Azobenzenearsonate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25869,T3D1303,p-Azobenzenearsonate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25870,T3D1303,p-Azobenzenearsonate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25871,T3D1303,p-Azobenzenearsonate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25872,T3D1303,p-Azobenzenearsonate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25873,T3D1303,p-Azobenzenearsonate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25874,T3D1303,p-Azobenzenearsonate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25875,T3D1303,p-Azobenzenearsonate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25876,T3D1303,p-Azobenzenearsonate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25877,T3D1303,p-Azobenzenearsonate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25878,T3D1304,"1,2-Bis(dimethylarsino)benzene","Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25879,T3D1304,"1,2-Bis(dimethylarsino)benzene","Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25880,T3D1304,"1,2-Bis(dimethylarsino)benzene","Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25881,T3D1304,"1,2-Bis(dimethylarsino)benzene","Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25882,T3D1304,"1,2-Bis(dimethylarsino)benzene","Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25883,T3D1304,"1,2-Bis(dimethylarsino)benzene","Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25884,T3D1304,"1,2-Bis(dimethylarsino)benzene","Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25885,T3D1304,"1,2-Bis(dimethylarsino)benzene",DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25886,T3D1304,"1,2-Bis(dimethylarsino)benzene",Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25887,T3D1304,"1,2-Bis(dimethylarsino)benzene",Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25888,T3D1304,"1,2-Bis(dimethylarsino)benzene","Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25889,T3D1304,"1,2-Bis(dimethylarsino)benzene",Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25890,T3D1304,"1,2-Bis(dimethylarsino)benzene",Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25891,T3D1304,"1,2-Bis(dimethylarsino)benzene",Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25892,T3D1304,"1,2-Bis(dimethylarsino)benzene",Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25893,T3D1304,"1,2-Bis(dimethylarsino)benzene",Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25894,T3D1304,"1,2-Bis(dimethylarsino)benzene",Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25895,T3D1304,"1,2-Bis(dimethylarsino)benzene",Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25896,T3D1304,"1,2-Bis(dimethylarsino)benzene",Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25897,T3D1304,"1,2-Bis(dimethylarsino)benzene","Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25898,T3D1304,"1,2-Bis(dimethylarsino)benzene","Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25899,T3D1304,"1,2-Bis(dimethylarsino)benzene","Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25900,T3D1304,"1,2-Bis(dimethylarsino)benzene","Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25901,T3D1304,"1,2-Bis(dimethylarsino)benzene","Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25902,T3D1304,"1,2-Bis(dimethylarsino)benzene","Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25903,T3D1304,"1,2-Bis(dimethylarsino)benzene",Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25904,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25905,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25906,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25907,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25908,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25909,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25910,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25911,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25912,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25913,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25914,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25915,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25916,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25917,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25918,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25919,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25920,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25921,T3D1304,"1,2-Bis(dimethylarsino)benzene",Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25922,T3D1305,Cacodyl,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25923,T3D1305,Cacodyl,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25924,T3D1305,Cacodyl,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25925,T3D1305,Cacodyl,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25926,T3D1305,Cacodyl,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25927,T3D1305,Cacodyl,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25928,T3D1305,Cacodyl,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25929,T3D1305,Cacodyl,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25930,T3D1305,Cacodyl,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25931,T3D1305,Cacodyl,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25932,T3D1305,Cacodyl,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25933,T3D1305,Cacodyl,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25934,T3D1305,Cacodyl,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25935,T3D1305,Cacodyl,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25936,T3D1305,Cacodyl,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25937,T3D1305,Cacodyl,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25938,T3D1305,Cacodyl,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25939,T3D1305,Cacodyl,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25940,T3D1305,Cacodyl,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25941,T3D1305,Cacodyl,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25942,T3D1305,Cacodyl,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25943,T3D1305,Cacodyl,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25944,T3D1305,Cacodyl,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25945,T3D1305,Cacodyl,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25946,T3D1305,Cacodyl,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25947,T3D1305,Cacodyl,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25948,T3D1305,Cacodyl,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25949,T3D1305,Cacodyl,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25950,T3D1305,Cacodyl,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25951,T3D1305,Cacodyl,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25952,T3D1305,Cacodyl,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25953,T3D1305,Cacodyl,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25954,T3D1305,Cacodyl,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25955,T3D1305,Cacodyl,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25956,T3D1305,Cacodyl,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25957,T3D1305,Cacodyl,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25958,T3D1305,Cacodyl,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25959,T3D1305,Cacodyl,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25960,T3D1305,Cacodyl,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25961,T3D1305,Cacodyl,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25962,T3D1305,Cacodyl,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25963,T3D1305,Cacodyl,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25964,T3D1305,Cacodyl,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25965,T3D1305,Cacodyl,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25966,T3D1306,Cacodyl oxide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
25967,T3D1306,Cacodyl oxide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
25968,T3D1306,Cacodyl oxide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
25969,T3D1306,Cacodyl oxide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
25970,T3D1306,Cacodyl oxide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
25971,T3D1306,Cacodyl oxide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
25972,T3D1306,Cacodyl oxide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25973,T3D1306,Cacodyl oxide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
25974,T3D1306,Cacodyl oxide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
25975,T3D1306,Cacodyl oxide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
25976,T3D1306,Cacodyl oxide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25977,T3D1306,Cacodyl oxide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
25978,T3D1306,Cacodyl oxide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
25979,T3D1306,Cacodyl oxide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
25980,T3D1306,Cacodyl oxide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
25981,T3D1306,Cacodyl oxide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
25982,T3D1306,Cacodyl oxide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25983,T3D1306,Cacodyl oxide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25984,T3D1306,Cacodyl oxide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25985,T3D1306,Cacodyl oxide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25986,T3D1306,Cacodyl oxide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25987,T3D1306,Cacodyl oxide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25988,T3D1306,Cacodyl oxide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
25989,T3D1306,Cacodyl oxide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25990,T3D1306,Cacodyl oxide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25991,T3D1306,Cacodyl oxide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
25992,T3D1306,Cacodyl oxide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25993,T3D1306,Cacodyl oxide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25994,T3D1306,Cacodyl oxide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25995,T3D1306,Cacodyl oxide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25996,T3D1306,Cacodyl oxide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25997,T3D1306,Cacodyl oxide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25998,T3D1306,Cacodyl oxide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
25999,T3D1306,Cacodyl oxide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26000,T3D1306,Cacodyl oxide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26001,T3D1306,Cacodyl oxide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26002,T3D1306,Cacodyl oxide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26003,T3D1306,Cacodyl oxide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26004,T3D1306,Cacodyl oxide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26005,T3D1306,Cacodyl oxide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26006,T3D1306,Cacodyl oxide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26007,T3D1306,Cacodyl oxide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26008,T3D1306,Cacodyl oxide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26009,T3D1306,Cacodyl oxide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26010,T3D1307,Diphenylchlorarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26011,T3D1307,Diphenylchlorarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26012,T3D1307,Diphenylchlorarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26013,T3D1307,Diphenylchlorarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26014,T3D1307,Diphenylchlorarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26015,T3D1307,Diphenylchlorarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26016,T3D1307,Diphenylchlorarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26017,T3D1307,Diphenylchlorarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26018,T3D1307,Diphenylchlorarsine,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
26019,T3D1307,Diphenylchlorarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26020,T3D1307,Diphenylchlorarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26021,T3D1307,Diphenylchlorarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26022,T3D1307,Diphenylchlorarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26023,T3D1307,Diphenylchlorarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26024,T3D1307,Diphenylchlorarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26025,T3D1307,Diphenylchlorarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26026,T3D1307,Diphenylchlorarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26027,T3D1307,Diphenylchlorarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26028,T3D1307,Diphenylchlorarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26029,T3D1307,Diphenylchlorarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26030,T3D1307,Diphenylchlorarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26031,T3D1307,Diphenylchlorarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26032,T3D1307,Diphenylchlorarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26033,T3D1307,Diphenylchlorarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26034,T3D1307,Diphenylchlorarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26035,T3D1307,Diphenylchlorarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26036,T3D1307,Diphenylchlorarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26037,T3D1307,Diphenylchlorarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26038,T3D1307,Diphenylchlorarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26039,T3D1307,Diphenylchlorarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26040,T3D1307,Diphenylchlorarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26041,T3D1307,Diphenylchlorarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26042,T3D1307,Diphenylchlorarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26043,T3D1307,Diphenylchlorarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26044,T3D1307,Diphenylchlorarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26045,T3D1307,Diphenylchlorarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26046,T3D1307,Diphenylchlorarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26047,T3D1307,Diphenylchlorarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26048,T3D1307,Diphenylchlorarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26049,T3D1307,Diphenylchlorarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26050,T3D1307,Diphenylchlorarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26051,T3D1307,Diphenylchlorarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26052,T3D1307,Diphenylchlorarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26053,T3D1307,Diphenylchlorarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26054,T3D1308,Diphenylcyanoarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26055,T3D1308,Diphenylcyanoarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26056,T3D1308,Diphenylcyanoarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26057,T3D1308,Diphenylcyanoarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26058,T3D1308,Diphenylcyanoarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26059,T3D1308,Diphenylcyanoarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26060,T3D1308,Diphenylcyanoarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26061,T3D1308,Diphenylcyanoarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26062,T3D1308,Diphenylcyanoarsine,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
26063,T3D1308,Diphenylcyanoarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26064,T3D1308,Diphenylcyanoarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26065,T3D1308,Diphenylcyanoarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26066,T3D1308,Diphenylcyanoarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26067,T3D1308,Diphenylcyanoarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26068,T3D1308,Diphenylcyanoarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26069,T3D1308,Diphenylcyanoarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26070,T3D1308,Diphenylcyanoarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26071,T3D1308,Diphenylcyanoarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26072,T3D1308,Diphenylcyanoarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26073,T3D1308,Diphenylcyanoarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26074,T3D1308,Diphenylcyanoarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26075,T3D1308,Diphenylcyanoarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26076,T3D1308,Diphenylcyanoarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26077,T3D1308,Diphenylcyanoarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26078,T3D1308,Diphenylcyanoarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26079,T3D1308,Diphenylcyanoarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26080,T3D1308,Diphenylcyanoarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26081,T3D1308,Diphenylcyanoarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26082,T3D1308,Diphenylcyanoarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26083,T3D1308,Diphenylcyanoarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26084,T3D1308,Diphenylcyanoarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26085,T3D1308,Diphenylcyanoarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26086,T3D1308,Diphenylcyanoarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26087,T3D1308,Diphenylcyanoarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26088,T3D1308,Diphenylcyanoarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26089,T3D1308,Diphenylcyanoarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26090,T3D1308,Diphenylcyanoarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26091,T3D1308,Diphenylcyanoarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26092,T3D1308,Diphenylcyanoarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26093,T3D1308,Diphenylcyanoarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26094,T3D1308,Diphenylcyanoarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26095,T3D1308,Diphenylcyanoarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26096,T3D1308,Diphenylcyanoarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26097,T3D1308,Diphenylcyanoarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26098,T3D1309,Ethyldichloroarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26099,T3D1309,Ethyldichloroarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26100,T3D1309,Ethyldichloroarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26101,T3D1309,Ethyldichloroarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26102,T3D1309,Ethyldichloroarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26103,T3D1309,Ethyldichloroarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26104,T3D1309,Ethyldichloroarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26105,T3D1309,Ethyldichloroarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26106,T3D1309,Ethyldichloroarsine,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
26107,T3D1309,Ethyldichloroarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26108,T3D1309,Ethyldichloroarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26109,T3D1309,Ethyldichloroarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26110,T3D1309,Ethyldichloroarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26111,T3D1309,Ethyldichloroarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26112,T3D1309,Ethyldichloroarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26113,T3D1309,Ethyldichloroarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26114,T3D1309,Ethyldichloroarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26115,T3D1309,Ethyldichloroarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26116,T3D1309,Ethyldichloroarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26117,T3D1309,Ethyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26118,T3D1309,Ethyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26119,T3D1309,Ethyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26120,T3D1309,Ethyldichloroarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26121,T3D1309,Ethyldichloroarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26122,T3D1309,Ethyldichloroarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26123,T3D1309,Ethyldichloroarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26124,T3D1309,Ethyldichloroarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26125,T3D1309,Ethyldichloroarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26126,T3D1309,Ethyldichloroarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26127,T3D1309,Ethyldichloroarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26128,T3D1309,Ethyldichloroarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26129,T3D1309,Ethyldichloroarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26130,T3D1309,Ethyldichloroarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26131,T3D1309,Ethyldichloroarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26132,T3D1309,Ethyldichloroarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26133,T3D1309,Ethyldichloroarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26134,T3D1309,Ethyldichloroarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26135,T3D1309,Ethyldichloroarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26136,T3D1309,Ethyldichloroarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26137,T3D1309,Ethyldichloroarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26138,T3D1309,Ethyldichloroarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26139,T3D1309,Ethyldichloroarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26140,T3D1309,Ethyldichloroarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26141,T3D1309,Ethyldichloroarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26142,T3D1310,Lewisite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26143,T3D1310,Lewisite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26144,T3D1310,Lewisite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26145,T3D1310,Lewisite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26146,T3D1310,Lewisite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26147,T3D1310,Lewisite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26148,T3D1310,Lewisite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26149,T3D1310,Lewisite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26150,T3D1310,Lewisite,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
26151,T3D1310,Lewisite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26152,T3D1310,Lewisite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26153,T3D1310,Lewisite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26154,T3D1310,Lewisite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26155,T3D1310,Lewisite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26156,T3D1310,Lewisite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26157,T3D1310,Lewisite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26158,T3D1310,Lewisite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26159,T3D1310,Lewisite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26160,T3D1310,Lewisite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26161,T3D1310,Lewisite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26162,T3D1310,Lewisite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26163,T3D1310,Lewisite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26164,T3D1310,Lewisite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26165,T3D1310,Lewisite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26166,T3D1310,Lewisite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26167,T3D1310,Lewisite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26168,T3D1310,Lewisite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26169,T3D1310,Lewisite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26170,T3D1310,Lewisite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26171,T3D1310,Lewisite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26172,T3D1310,Lewisite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26173,T3D1310,Lewisite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26174,T3D1310,Lewisite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26175,T3D1310,Lewisite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26176,T3D1310,Lewisite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26177,T3D1310,Lewisite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26178,T3D1310,Lewisite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26179,T3D1310,Lewisite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26180,T3D1310,Lewisite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26181,T3D1310,Lewisite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26182,T3D1310,Lewisite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26183,T3D1310,Lewisite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26184,T3D1310,Lewisite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26185,T3D1310,Lewisite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26186,T3D1311,Methyldichloroarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26187,T3D1311,Methyldichloroarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26188,T3D1311,Methyldichloroarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26189,T3D1311,Methyldichloroarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26190,T3D1311,Methyldichloroarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26191,T3D1311,Methyldichloroarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26192,T3D1311,Methyldichloroarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26193,T3D1311,Methyldichloroarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26194,T3D1311,Methyldichloroarsine,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
26195,T3D1311,Methyldichloroarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26196,T3D1311,Methyldichloroarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26197,T3D1311,Methyldichloroarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26198,T3D1311,Methyldichloroarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26199,T3D1311,Methyldichloroarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26200,T3D1311,Methyldichloroarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26201,T3D1311,Methyldichloroarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26202,T3D1311,Methyldichloroarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26203,T3D1311,Methyldichloroarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26204,T3D1311,Methyldichloroarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26205,T3D1311,Methyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26206,T3D1311,Methyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26207,T3D1311,Methyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26208,T3D1311,Methyldichloroarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26209,T3D1311,Methyldichloroarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26210,T3D1311,Methyldichloroarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26211,T3D1311,Methyldichloroarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26212,T3D1311,Methyldichloroarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26213,T3D1311,Methyldichloroarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26214,T3D1311,Methyldichloroarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26215,T3D1311,Methyldichloroarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26216,T3D1311,Methyldichloroarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26217,T3D1311,Methyldichloroarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26218,T3D1311,Methyldichloroarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26219,T3D1311,Methyldichloroarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26220,T3D1311,Methyldichloroarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26221,T3D1311,Methyldichloroarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26222,T3D1311,Methyldichloroarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26223,T3D1311,Methyldichloroarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26224,T3D1311,Methyldichloroarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26225,T3D1311,Methyldichloroarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26226,T3D1311,Methyldichloroarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26227,T3D1311,Methyldichloroarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26228,T3D1311,Methyldichloroarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26229,T3D1311,Methyldichloroarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26230,T3D1312,Phenyldichloroarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26231,T3D1312,Phenyldichloroarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26232,T3D1312,Phenyldichloroarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26233,T3D1312,Phenyldichloroarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26234,T3D1312,Phenyldichloroarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26235,T3D1312,Phenyldichloroarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26236,T3D1312,Phenyldichloroarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26237,T3D1312,Phenyldichloroarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26238,T3D1312,Phenyldichloroarsine,Estrogen receptor,P03372,Causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (S301)
26239,T3D1312,Phenyldichloroarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26240,T3D1312,Phenyldichloroarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26241,T3D1312,Phenyldichloroarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26242,T3D1312,Phenyldichloroarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26243,T3D1312,Phenyldichloroarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26244,T3D1312,Phenyldichloroarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26245,T3D1312,Phenyldichloroarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26246,T3D1312,Phenyldichloroarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26247,T3D1312,Phenyldichloroarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26248,T3D1312,Phenyldichloroarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26249,T3D1312,Phenyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26250,T3D1312,Phenyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26251,T3D1312,Phenyldichloroarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26252,T3D1312,Phenyldichloroarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26253,T3D1312,Phenyldichloroarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26254,T3D1312,Phenyldichloroarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26255,T3D1312,Phenyldichloroarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26256,T3D1312,Phenyldichloroarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26257,T3D1312,Phenyldichloroarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26258,T3D1312,Phenyldichloroarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26259,T3D1312,Phenyldichloroarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26260,T3D1312,Phenyldichloroarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26261,T3D1312,Phenyldichloroarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26262,T3D1312,Phenyldichloroarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26263,T3D1312,Phenyldichloroarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26264,T3D1312,Phenyldichloroarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26265,T3D1312,Phenyldichloroarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26266,T3D1312,Phenyldichloroarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26267,T3D1312,Phenyldichloroarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26268,T3D1312,Phenyldichloroarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26269,T3D1312,Phenyldichloroarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26270,T3D1312,Phenyldichloroarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26271,T3D1312,Phenyldichloroarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26272,T3D1312,Phenyldichloroarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26273,T3D1312,Phenyldichloroarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26274,T3D1313,Thorin,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26275,T3D1313,Thorin,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26276,T3D1313,Thorin,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26277,T3D1313,Thorin,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26278,T3D1313,Thorin,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26279,T3D1313,Thorin,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26280,T3D1313,Thorin,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26281,T3D1313,Thorin,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26282,T3D1313,Thorin,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26283,T3D1313,Thorin,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26284,T3D1313,Thorin,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26285,T3D1313,Thorin,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26286,T3D1313,Thorin,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26287,T3D1313,Thorin,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26288,T3D1313,Thorin,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26289,T3D1313,Thorin,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26290,T3D1313,Thorin,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26291,T3D1313,Thorin,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26292,T3D1313,Thorin,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26293,T3D1313,Thorin,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26294,T3D1313,Thorin,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26295,T3D1313,Thorin,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26296,T3D1313,Thorin,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26297,T3D1313,Thorin,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26298,T3D1313,Thorin,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26299,T3D1313,Thorin,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26300,T3D1313,Thorin,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26301,T3D1313,Thorin,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26302,T3D1313,Thorin,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26303,T3D1313,Thorin,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26304,T3D1313,Thorin,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26305,T3D1313,Thorin,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26306,T3D1313,Thorin,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26307,T3D1313,Thorin,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26308,T3D1313,Thorin,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26309,T3D1313,Thorin,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26310,T3D1313,Thorin,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26311,T3D1313,Thorin,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26312,T3D1313,Thorin,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26313,T3D1313,Thorin,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26314,T3D1313,Thorin,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26315,T3D1313,Thorin,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26316,T3D1313,Thorin,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26317,T3D1313,Thorin,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26318,T3D1314,Triphenylarsine,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26319,T3D1314,Triphenylarsine,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26320,T3D1314,Triphenylarsine,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26321,T3D1314,Triphenylarsine,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26322,T3D1314,Triphenylarsine,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26323,T3D1314,Triphenylarsine,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26324,T3D1314,Triphenylarsine,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26325,T3D1314,Triphenylarsine,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26326,T3D1314,Triphenylarsine,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26327,T3D1314,Triphenylarsine,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26328,T3D1314,Triphenylarsine,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26329,T3D1314,Triphenylarsine,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26330,T3D1314,Triphenylarsine,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26331,T3D1314,Triphenylarsine,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26332,T3D1314,Triphenylarsine,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26333,T3D1314,Triphenylarsine,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26334,T3D1314,Triphenylarsine,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26335,T3D1314,Triphenylarsine,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26336,T3D1314,Triphenylarsine,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26337,T3D1314,Triphenylarsine,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26338,T3D1314,Triphenylarsine,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26339,T3D1314,Triphenylarsine,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26340,T3D1314,Triphenylarsine,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26341,T3D1314,Triphenylarsine,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26342,T3D1314,Triphenylarsine,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26343,T3D1314,Triphenylarsine,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26344,T3D1314,Triphenylarsine,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26345,T3D1314,Triphenylarsine,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26346,T3D1314,Triphenylarsine,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26347,T3D1314,Triphenylarsine,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26348,T3D1314,Triphenylarsine,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26349,T3D1314,Triphenylarsine,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26350,T3D1314,Triphenylarsine,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26351,T3D1314,Triphenylarsine,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26352,T3D1314,Triphenylarsine,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26353,T3D1314,Triphenylarsine,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26354,T3D1314,Triphenylarsine,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26355,T3D1314,Triphenylarsine,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26356,T3D1314,Triphenylarsine,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26357,T3D1314,Triphenylarsine,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26358,T3D1314,Triphenylarsine,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26359,T3D1314,Triphenylarsine,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26360,T3D1314,Triphenylarsine,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26361,T3D1314,Triphenylarsine,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26362,T3D1315,Sodium arsenate heptahydrate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26363,T3D1315,Sodium arsenate heptahydrate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26364,T3D1315,Sodium arsenate heptahydrate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26365,T3D1315,Sodium arsenate heptahydrate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26366,T3D1315,Sodium arsenate heptahydrate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26367,T3D1315,Sodium arsenate heptahydrate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26368,T3D1315,Sodium arsenate heptahydrate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26369,T3D1315,Sodium arsenate heptahydrate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26370,T3D1315,Sodium arsenate heptahydrate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26371,T3D1315,Sodium arsenate heptahydrate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26372,T3D1315,Sodium arsenate heptahydrate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26373,T3D1315,Sodium arsenate heptahydrate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26374,T3D1315,Sodium arsenate heptahydrate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26375,T3D1315,Sodium arsenate heptahydrate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26376,T3D1315,Sodium arsenate heptahydrate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26377,T3D1315,Sodium arsenate heptahydrate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26378,T3D1315,Sodium arsenate heptahydrate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26379,T3D1315,Sodium arsenate heptahydrate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26380,T3D1315,Sodium arsenate heptahydrate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26381,T3D1315,Sodium arsenate heptahydrate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26382,T3D1315,Sodium arsenate heptahydrate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26383,T3D1315,Sodium arsenate heptahydrate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26384,T3D1315,Sodium arsenate heptahydrate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26385,T3D1315,Sodium arsenate heptahydrate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26386,T3D1315,Sodium arsenate heptahydrate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26387,T3D1315,Sodium arsenate heptahydrate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26388,T3D1315,Sodium arsenate heptahydrate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26389,T3D1315,Sodium arsenate heptahydrate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26390,T3D1315,Sodium arsenate heptahydrate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26391,T3D1315,Sodium arsenate heptahydrate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26392,T3D1315,Sodium arsenate heptahydrate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26393,T3D1315,Sodium arsenate heptahydrate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26394,T3D1315,Sodium arsenate heptahydrate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26395,T3D1315,Sodium arsenate heptahydrate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26396,T3D1315,Sodium arsenate heptahydrate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26397,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26398,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26399,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26400,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26401,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26402,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26403,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26404,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26405,T3D1315,Sodium arsenate heptahydrate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26406,T3D1316,Calcium arsenite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26407,T3D1316,Calcium arsenite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26408,T3D1316,Calcium arsenite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26409,T3D1316,Calcium arsenite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26410,T3D1316,Calcium arsenite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26411,T3D1316,Calcium arsenite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26412,T3D1316,Calcium arsenite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26413,T3D1316,Calcium arsenite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26414,T3D1316,Calcium arsenite,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26415,T3D1316,Calcium arsenite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26416,T3D1316,Calcium arsenite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26417,T3D1316,Calcium arsenite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26418,T3D1316,Calcium arsenite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26419,T3D1316,Calcium arsenite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26420,T3D1316,Calcium arsenite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26421,T3D1316,Calcium arsenite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26422,T3D1316,Calcium arsenite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26423,T3D1316,Calcium arsenite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26424,T3D1316,Calcium arsenite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26425,T3D1316,Calcium arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26426,T3D1316,Calcium arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26427,T3D1316,Calcium arsenite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26428,T3D1316,Calcium arsenite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26429,T3D1316,Calcium arsenite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26430,T3D1316,Calcium arsenite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26431,T3D1316,Calcium arsenite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26432,T3D1316,Calcium arsenite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26433,T3D1316,Calcium arsenite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26434,T3D1316,Calcium arsenite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26435,T3D1316,Calcium arsenite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26436,T3D1316,Calcium arsenite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26437,T3D1316,Calcium arsenite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26438,T3D1316,Calcium arsenite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26439,T3D1316,Calcium arsenite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26440,T3D1316,Calcium arsenite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26441,T3D1316,Calcium arsenite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26442,T3D1316,Calcium arsenite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26443,T3D1316,Calcium arsenite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26444,T3D1316,Calcium arsenite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26445,T3D1316,Calcium arsenite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26446,T3D1316,Calcium arsenite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26447,T3D1316,Calcium arsenite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26448,T3D1316,Calcium arsenite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26449,T3D1316,Calcium arsenite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26450,T3D1317,Strontium arsenite tetrahydrate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26451,T3D1317,Strontium arsenite tetrahydrate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26452,T3D1317,Strontium arsenite tetrahydrate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26453,T3D1317,Strontium arsenite tetrahydrate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26454,T3D1317,Strontium arsenite tetrahydrate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26455,T3D1317,Strontium arsenite tetrahydrate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26456,T3D1317,Strontium arsenite tetrahydrate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26457,T3D1317,Strontium arsenite tetrahydrate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26458,T3D1317,Strontium arsenite tetrahydrate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26459,T3D1317,Strontium arsenite tetrahydrate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26460,T3D1317,Strontium arsenite tetrahydrate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26461,T3D1317,Strontium arsenite tetrahydrate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26462,T3D1317,Strontium arsenite tetrahydrate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26463,T3D1317,Strontium arsenite tetrahydrate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26464,T3D1317,Strontium arsenite tetrahydrate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26465,T3D1317,Strontium arsenite tetrahydrate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26466,T3D1317,Strontium arsenite tetrahydrate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26467,T3D1317,Strontium arsenite tetrahydrate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26468,T3D1317,Strontium arsenite tetrahydrate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26469,T3D1317,Strontium arsenite tetrahydrate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26470,T3D1317,Strontium arsenite tetrahydrate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26471,T3D1317,Strontium arsenite tetrahydrate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26472,T3D1317,Strontium arsenite tetrahydrate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26473,T3D1317,Strontium arsenite tetrahydrate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26474,T3D1317,Strontium arsenite tetrahydrate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26475,T3D1317,Strontium arsenite tetrahydrate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26476,T3D1317,Strontium arsenite tetrahydrate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26477,T3D1317,Strontium arsenite tetrahydrate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26478,T3D1317,Strontium arsenite tetrahydrate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26479,T3D1317,Strontium arsenite tetrahydrate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26480,T3D1317,Strontium arsenite tetrahydrate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26481,T3D1317,Strontium arsenite tetrahydrate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26482,T3D1317,Strontium arsenite tetrahydrate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26483,T3D1317,Strontium arsenite tetrahydrate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26484,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26485,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26486,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26487,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26488,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26489,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26490,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26491,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26492,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26493,T3D1317,Strontium arsenite tetrahydrate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26494,T3D1318,Ferrous arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26495,T3D1318,Ferrous arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26496,T3D1318,Ferrous arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26497,T3D1318,Ferrous arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26498,T3D1318,Ferrous arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26499,T3D1318,Ferrous arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26500,T3D1318,Ferrous arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26501,T3D1318,Ferrous arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26502,T3D1318,Ferrous arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26503,T3D1318,Ferrous arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26504,T3D1318,Ferrous arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26505,T3D1318,Ferrous arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26506,T3D1318,Ferrous arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26507,T3D1318,Ferrous arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26508,T3D1318,Ferrous arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26509,T3D1318,Ferrous arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26510,T3D1318,Ferrous arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26511,T3D1318,Ferrous arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26512,T3D1318,Ferrous arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26513,T3D1318,Ferrous arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26514,T3D1318,Ferrous arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26515,T3D1318,Ferrous arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26516,T3D1318,Ferrous arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26517,T3D1318,Ferrous arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26518,T3D1318,Ferrous arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26519,T3D1318,Ferrous arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26520,T3D1318,Ferrous arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26521,T3D1318,Ferrous arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26522,T3D1318,Ferrous arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26523,T3D1318,Ferrous arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26524,T3D1318,Ferrous arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26525,T3D1318,Ferrous arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26526,T3D1318,Ferrous arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26527,T3D1318,Ferrous arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26528,T3D1318,Ferrous arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26529,T3D1318,Ferrous arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26530,T3D1318,Ferrous arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26531,T3D1318,Ferrous arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26532,T3D1318,Ferrous arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26533,T3D1318,Ferrous arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26534,T3D1318,Ferrous arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26535,T3D1318,Ferrous arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26536,T3D1318,Ferrous arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26537,T3D1318,Ferrous arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26538,T3D1319,Ferric arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26539,T3D1319,Ferric arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26540,T3D1319,Ferric arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26541,T3D1319,Ferric arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26542,T3D1319,Ferric arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26543,T3D1319,Ferric arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26544,T3D1319,Ferric arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26545,T3D1319,Ferric arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26546,T3D1319,Ferric arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26547,T3D1319,Ferric arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26548,T3D1319,Ferric arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26549,T3D1319,Ferric arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26550,T3D1319,Ferric arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26551,T3D1319,Ferric arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26552,T3D1319,Ferric arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26553,T3D1319,Ferric arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26554,T3D1319,Ferric arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26555,T3D1319,Ferric arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26556,T3D1319,Ferric arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26557,T3D1319,Ferric arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26558,T3D1319,Ferric arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26559,T3D1319,Ferric arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26560,T3D1319,Ferric arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26561,T3D1319,Ferric arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26562,T3D1319,Ferric arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26563,T3D1319,Ferric arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26564,T3D1319,Ferric arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26565,T3D1319,Ferric arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26566,T3D1319,Ferric arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26567,T3D1319,Ferric arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26568,T3D1319,Ferric arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26569,T3D1319,Ferric arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26570,T3D1319,Ferric arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26571,T3D1319,Ferric arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26572,T3D1319,Ferric arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26573,T3D1319,Ferric arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26574,T3D1319,Ferric arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26575,T3D1319,Ferric arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26576,T3D1319,Ferric arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26577,T3D1319,Ferric arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26578,T3D1319,Ferric arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26579,T3D1319,Ferric arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26580,T3D1319,Ferric arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26581,T3D1319,Ferric arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26582,T3D1320,Iron cacodylate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26583,T3D1320,Iron cacodylate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26584,T3D1320,Iron cacodylate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26585,T3D1320,Iron cacodylate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26586,T3D1320,Iron cacodylate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26587,T3D1320,Iron cacodylate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26588,T3D1320,Iron cacodylate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26589,T3D1320,Iron cacodylate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26590,T3D1320,Iron cacodylate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26591,T3D1320,Iron cacodylate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26592,T3D1320,Iron cacodylate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26593,T3D1320,Iron cacodylate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26594,T3D1320,Iron cacodylate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26595,T3D1320,Iron cacodylate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26596,T3D1320,Iron cacodylate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26597,T3D1320,Iron cacodylate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26598,T3D1320,Iron cacodylate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26599,T3D1320,Iron cacodylate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26600,T3D1320,Iron cacodylate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26601,T3D1320,Iron cacodylate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26602,T3D1320,Iron cacodylate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26603,T3D1320,Iron cacodylate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26604,T3D1320,Iron cacodylate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26605,T3D1320,Iron cacodylate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26606,T3D1320,Iron cacodylate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26607,T3D1320,Iron cacodylate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26608,T3D1320,Iron cacodylate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26609,T3D1320,Iron cacodylate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26610,T3D1320,Iron cacodylate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26611,T3D1320,Iron cacodylate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26612,T3D1320,Iron cacodylate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26613,T3D1320,Iron cacodylate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26614,T3D1320,Iron cacodylate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26615,T3D1320,Iron cacodylate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26616,T3D1320,Iron cacodylate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26617,T3D1320,Iron cacodylate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26618,T3D1320,Iron cacodylate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26619,T3D1320,Iron cacodylate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26620,T3D1320,Iron cacodylate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26621,T3D1320,Iron cacodylate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26622,T3D1320,Iron cacodylate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26623,T3D1320,Iron cacodylate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26624,T3D1320,Iron cacodylate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26625,T3D1320,Iron cacodylate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26626,T3D1321,Phenarsazine oxide,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26627,T3D1321,Phenarsazine oxide,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26628,T3D1321,Phenarsazine oxide,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26629,T3D1321,Phenarsazine oxide,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26630,T3D1321,Phenarsazine oxide,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26631,T3D1321,Phenarsazine oxide,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26632,T3D1321,Phenarsazine oxide,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26633,T3D1321,Phenarsazine oxide,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26634,T3D1321,Phenarsazine oxide,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26635,T3D1321,Phenarsazine oxide,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26636,T3D1321,Phenarsazine oxide,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26637,T3D1321,Phenarsazine oxide,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26638,T3D1321,Phenarsazine oxide,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26639,T3D1321,Phenarsazine oxide,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26640,T3D1321,Phenarsazine oxide,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26641,T3D1321,Phenarsazine oxide,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26642,T3D1321,Phenarsazine oxide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26643,T3D1321,Phenarsazine oxide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26644,T3D1321,Phenarsazine oxide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26645,T3D1321,Phenarsazine oxide,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26646,T3D1321,Phenarsazine oxide,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26647,T3D1321,Phenarsazine oxide,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26648,T3D1321,Phenarsazine oxide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26649,T3D1321,Phenarsazine oxide,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26650,T3D1321,Phenarsazine oxide,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26651,T3D1321,Phenarsazine oxide,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26652,T3D1321,Phenarsazine oxide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26653,T3D1321,Phenarsazine oxide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26654,T3D1321,Phenarsazine oxide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26655,T3D1321,Phenarsazine oxide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26656,T3D1321,Phenarsazine oxide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26657,T3D1321,Phenarsazine oxide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26658,T3D1321,Phenarsazine oxide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26659,T3D1321,Phenarsazine oxide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26660,T3D1321,Phenarsazine oxide,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26661,T3D1321,Phenarsazine oxide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26662,T3D1321,Phenarsazine oxide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26663,T3D1321,Phenarsazine oxide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26664,T3D1321,Phenarsazine oxide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26665,T3D1321,Phenarsazine oxide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26666,T3D1321,Phenarsazine oxide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26667,T3D1321,Phenarsazine oxide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26668,T3D1321,Phenarsazine oxide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26669,T3D1321,Phenarsazine oxide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26670,T3D1409,Nickel arsenate,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26671,T3D1409,Nickel arsenate,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26672,T3D1409,Nickel arsenate,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26673,T3D1409,Nickel arsenate,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26674,T3D1409,Nickel arsenate,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26675,T3D1409,Nickel arsenate,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26676,T3D1409,Nickel arsenate,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26677,T3D1409,Nickel arsenate,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26678,T3D1409,Nickel arsenate,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26679,T3D1409,Nickel arsenate,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26680,T3D1409,Nickel arsenate,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26681,T3D1409,Nickel arsenate,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26682,T3D1409,Nickel arsenate,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26683,T3D1409,Nickel arsenate,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26684,T3D1409,Nickel arsenate,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26685,T3D1409,Nickel arsenate,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26686,T3D1409,Nickel arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26687,T3D1409,Nickel arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26688,T3D1409,Nickel arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26689,T3D1409,Nickel arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26690,T3D1409,Nickel arsenate,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26691,T3D1409,Nickel arsenate,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26692,T3D1409,Nickel arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26693,T3D1409,Nickel arsenate,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26694,T3D1409,Nickel arsenate,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26695,T3D1409,Nickel arsenate,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26696,T3D1409,Nickel arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26697,T3D1409,Nickel arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26698,T3D1409,Nickel arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26699,T3D1409,Nickel arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26700,T3D1409,Nickel arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26701,T3D1409,Nickel arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26702,T3D1409,Nickel arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26703,T3D1409,Nickel arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26704,T3D1409,Nickel arsenate,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26705,T3D1409,Nickel arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26706,T3D1409,Nickel arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26707,T3D1409,Nickel arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26708,T3D1409,Nickel arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26709,T3D1409,Nickel arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26710,T3D1409,Nickel arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26711,T3D1409,Nickel arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26712,T3D1409,Nickel arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26713,T3D1409,Nickel arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26714,T3D1459,Zinc arsenite,"Actin, alpha cardiac muscle 1",P68032,Arsenic binds to actin. (R053)
26715,T3D1459,Zinc arsenite,"Actin, alpha skeletal muscle",P68133,Arsenic binds to actin. (R053)
26716,T3D1459,Zinc arsenite,"Actin, aortic smooth muscle",P62736,Arsenic binds to actin. (R053)
26717,T3D1459,Zinc arsenite,"Actin, cytoplasmic 1",P60709,Arsenic binds to actin. (R053)
26718,T3D1459,Zinc arsenite,"Actin, cytoplasmic 2",P63261,Arsenic binds to actin. (R053)
26719,T3D1459,Zinc arsenite,"Actin, gamma-enteric smooth muscle",P63267,Arsenic binds to actin. (R053)
26720,T3D1459,Zinc arsenite,"Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial",P10515,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26721,T3D1459,Zinc arsenite,DNA repair protein complementing XP-A cells,P23025,Arsenic binding of XPA is believed to induce carcinogenesis by affecting DNA repair. (R054)
26722,T3D1459,Zinc arsenite,Estrogen receptor,P03372,Arsenic binds to the estrogen receptor. (R054)
26723,T3D1459,Zinc arsenite,Glucocorticoid receptor,P04150,Arsenic binds to the glucocorticoid receptor. (R054)
26724,T3D1459,Zinc arsenite,"Glutathione reductase, mitochondrial",P00390,"Arsenic binds glutathione reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26725,T3D1459,Zinc arsenite,Haptoglobin,P00738,Arsenic binds to haptoglobin. (R052)
26726,T3D1459,Zinc arsenite,Hemoglobin subunit alpha,P69905,Arsenic binds to hemoglobin. (R052)
26727,T3D1459,Zinc arsenite,Hemoglobin subunit beta,P68871,Arsenic binds to hemoglobin. (R052)
26728,T3D1459,Zinc arsenite,Kelch-like ECH-associated protein 1,Q14145,Arsenic binds to kelch-like ECH-associated protein 1. (R054)
26729,T3D1459,Zinc arsenite,Poly [ADP-ribose] polymerase 1,P09874,Arsenic binding of PARP-1 is believed to induce carcinogenesis by affecting DNA repair. (R054)
26730,T3D1459,Zinc arsenite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26731,T3D1459,Zinc arsenite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26732,T3D1459,Zinc arsenite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26733,T3D1459,Zinc arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial",P08559,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26734,T3D1459,Zinc arsenite,"Pyruvate dehydrogenase E1 component subunit alpha, testis-specific form, mitochondrial",P29803,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26735,T3D1459,Zinc arsenite,"Pyruvate dehydrogenase E1 component subunit beta, mitochondrial",P11177,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26736,T3D1459,Zinc arsenite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26737,T3D1459,Zinc arsenite,"Thioredoxin reductase 1, cytoplasmic",Q16881,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26738,T3D1459,Zinc arsenite,"Thioredoxin reductase 2, mitochondrial",Q9NNW7,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26739,T3D1459,Zinc arsenite,Thioredoxin reductase 3,Q86VQ6,"Arsenic binds thioredoxin reductase, which results in the inhibition of essential biochemical reactions, alteration of cellular redox status, and eventual cytotoxicity. (R009)"
26740,T3D1459,Zinc arsenite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26741,T3D1459,Zinc arsenite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26742,T3D1459,Zinc arsenite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26743,T3D1459,Zinc arsenite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26744,T3D1459,Zinc arsenite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26745,T3D1459,Zinc arsenite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26746,T3D1459,Zinc arsenite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26747,T3D1459,Zinc arsenite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26748,T3D1459,Zinc arsenite,Tubulin beta chain,P07437,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26749,T3D1459,Zinc arsenite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26750,T3D1459,Zinc arsenite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26751,T3D1459,Zinc arsenite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26752,T3D1459,Zinc arsenite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26753,T3D1459,Zinc arsenite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26754,T3D1459,Zinc arsenite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26755,T3D1459,Zinc arsenite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26756,T3D1459,Zinc arsenite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26757,T3D1459,Zinc arsenite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26758,T3D0223,Arsenic acid,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26759,T3D0223,Arsenic acid,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26760,T3D0223,Arsenic acid,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26761,T3D0223,Arsenic acid,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26762,T3D0223,Arsenic acid,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26763,T3D0223,Arsenic acid,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26764,T3D0223,Arsenic acid,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26765,T3D0223,Arsenic acid,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26766,T3D0223,Arsenic acid,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26767,T3D0223,Arsenic acid,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26768,T3D0223,Arsenic acid,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26769,T3D0223,Arsenic acid,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26770,T3D0223,Arsenic acid,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26771,T3D0223,Arsenic acid,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26772,T3D0223,Arsenic acid,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26773,T3D0223,Arsenic acid,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26774,T3D0223,Arsenic acid,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26775,T3D0223,Arsenic acid,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26776,T3D0223,Arsenic acid,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26777,T3D0223,Arsenic acid,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26778,T3D0223,Arsenic acid,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26779,T3D0224,Arsenic trioxide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26780,T3D0224,Arsenic trioxide,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26781,T3D0224,Arsenic trioxide,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26782,T3D0224,Arsenic trioxide,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26783,T3D0224,Arsenic trioxide,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26784,T3D0224,Arsenic trioxide,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26785,T3D0224,Arsenic trioxide,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26786,T3D0224,Arsenic trioxide,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26787,T3D0224,Arsenic trioxide,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26788,T3D0224,Arsenic trioxide,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26789,T3D0224,Arsenic trioxide,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26790,T3D0224,Arsenic trioxide,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26791,T3D0224,Arsenic trioxide,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26792,T3D0224,Arsenic trioxide,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26793,T3D0224,Arsenic trioxide,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26794,T3D0224,Arsenic trioxide,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26795,T3D0224,Arsenic trioxide,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26796,T3D0224,Arsenic trioxide,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26797,T3D0224,Arsenic trioxide,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26798,T3D0224,Arsenic trioxide,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26799,T3D0224,Arsenic trioxide,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26800,T3D0241,Calcium arsenate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26801,T3D0241,Calcium arsenate,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26802,T3D0241,Calcium arsenate,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26803,T3D0241,Calcium arsenate,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26804,T3D0241,Calcium arsenate,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26805,T3D0241,Calcium arsenate,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26806,T3D0241,Calcium arsenate,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26807,T3D0241,Calcium arsenate,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26808,T3D0241,Calcium arsenate,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26809,T3D0241,Calcium arsenate,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26810,T3D0241,Calcium arsenate,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26811,T3D0241,Calcium arsenate,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26812,T3D0241,Calcium arsenate,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26813,T3D0241,Calcium arsenate,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26814,T3D0241,Calcium arsenate,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26815,T3D0241,Calcium arsenate,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26816,T3D0241,Calcium arsenate,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26817,T3D0241,Calcium arsenate,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26818,T3D0241,Calcium arsenate,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26819,T3D0241,Calcium arsenate,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26820,T3D0241,Calcium arsenate,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26821,T3D0243,Sodium arsenite,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26822,T3D0243,Sodium arsenite,Putative tubulin beta-4q chain,Q99867,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26823,T3D0243,Sodium arsenite,Putative tubulin-like protein alpha-4B,Q9H853,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26824,T3D0243,Sodium arsenite,"Pyruvate dehydrogenase protein X component, mitochondrial",O00330,"Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. (R001)"
26825,T3D0243,Sodium arsenite,Tubulin alpha chain-like 3,A6NHL2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26826,T3D0243,Sodium arsenite,Tubulin alpha-1A chain,Q71U36,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26827,T3D0243,Sodium arsenite,Tubulin alpha-1B chain,P68363,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26828,T3D0243,Sodium arsenite,Tubulin alpha-1C chain,Q9BQE3,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26829,T3D0243,Sodium arsenite,Tubulin alpha-3C/D chain,Q13748,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26830,T3D0243,Sodium arsenite,Tubulin alpha-3E chain,Q6PEY2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26831,T3D0243,Sodium arsenite,Tubulin alpha-4A chain,P68366,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26832,T3D0243,Sodium arsenite,Tubulin alpha-8 chain,Q9NY65,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26833,T3D0243,Sodium arsenite,Tubulin beta-1 chain,Q9H4B7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26834,T3D0243,Sodium arsenite,Tubulin beta-2A chain,Q13885,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26835,T3D0243,Sodium arsenite,Tubulin beta-2B chain,Q9BVA1,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26836,T3D0243,Sodium arsenite,Tubulin beta-2C chain,P68371,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26837,T3D0243,Sodium arsenite,Tubulin beta-3 chain,Q13509,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26838,T3D0243,Sodium arsenite,Tubulin beta-4 chain,P04350,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26839,T3D0243,Sodium arsenite,Tubulin beta-6 chain,Q9BUF5,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26840,T3D0243,Sodium arsenite,Tubulin beta-8 chain,Q3ZCM7,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26841,T3D0243,Sodium arsenite,Tubulin beta-8 chain B,A6NNZ2,"Arsenic's carginogenicity is believed to be caused by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. (R054)"
26842,T3D0320,Lead arsenite,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26843,T3D0320,Lead arsenite,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26844,T3D0320,Lead arsenite,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26845,T3D0320,Lead arsenite,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26846,T3D0320,Lead arsenite,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26847,T3D0321,Lead azide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26848,T3D0321,Lead azide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26849,T3D0321,Lead azide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26850,T3D0321,Lead azide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26851,T3D0321,Lead azide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26852,T3D0322,Lead bromide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26853,T3D0322,Lead bromide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26854,T3D0322,Lead bromide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26855,T3D0322,Lead bromide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26856,T3D0322,Lead bromide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26857,T3D0323,Lead carbonate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26858,T3D0323,Lead carbonate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26859,T3D0323,Lead carbonate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26860,T3D0323,Lead carbonate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26861,T3D0323,Lead carbonate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26862,T3D0324,Lead chloride,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26863,T3D0324,Lead chloride,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26864,T3D0324,Lead chloride,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26865,T3D0324,Lead chloride,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26866,T3D0324,Lead chloride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26867,T3D0325,Lead chromate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26868,T3D0325,Lead chromate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26869,T3D0325,Lead chromate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26870,T3D0325,Lead chromate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26871,T3D0325,Lead chromate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26872,T3D0326,Lead fluoroborate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26873,T3D0326,Lead fluoroborate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26874,T3D0326,Lead fluoroborate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26875,T3D0326,Lead fluoroborate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26876,T3D0326,Lead fluoroborate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26877,T3D0327,Lead iodide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26878,T3D0327,Lead iodide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26879,T3D0327,Lead iodide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26880,T3D0327,Lead iodide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26881,T3D0327,Lead iodide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26882,T3D0328,Lead molybdenum chromate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26883,T3D0328,Lead molybdenum chromate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26884,T3D0328,Lead molybdenum chromate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26885,T3D0328,Lead molybdenum chromate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26886,T3D0328,Lead molybdenum chromate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26887,T3D0329,Lead nitrate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26888,T3D0329,Lead nitrate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26889,T3D0329,Lead nitrate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26890,T3D0329,Lead nitrate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26891,T3D0329,Lead nitrate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26892,T3D0330,Lead oxide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26893,T3D0330,Lead oxide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26894,T3D0330,Lead oxide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26895,T3D0330,Lead oxide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26896,T3D0330,Lead oxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26897,T3D0331,Lead dioxide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26898,T3D0331,Lead dioxide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26899,T3D0331,Lead dioxide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26900,T3D0331,Lead dioxide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26901,T3D0331,Lead dioxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26902,T3D0332,Lead tetroxide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26903,T3D0332,Lead tetroxide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26904,T3D0332,Lead tetroxide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26905,T3D0332,Lead tetroxide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26906,T3D0332,Lead tetroxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26907,T3D0333,Lead phosphate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26908,T3D0333,Lead phosphate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26909,T3D0333,Lead phosphate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26910,T3D0333,Lead phosphate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26911,T3D0333,Lead phosphate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26912,T3D0334,Lead styphnate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26913,T3D0334,Lead styphnate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26914,T3D0334,Lead styphnate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26915,T3D0334,Lead styphnate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26916,T3D0334,Lead styphnate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26917,T3D0335,Lead sulfate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26918,T3D0335,Lead sulfate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26919,T3D0335,Lead sulfate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26920,T3D0335,Lead sulfate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26921,T3D0335,Lead sulfate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26922,T3D0336,Lead sulfide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26923,T3D0336,Lead sulfide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26924,T3D0336,Lead sulfide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26925,T3D0336,Lead sulfide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26926,T3D0336,Lead sulfide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26927,T3D0337,Tetramethyl lead,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26928,T3D0337,Tetramethyl lead,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26929,T3D0337,Tetramethyl lead,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26930,T3D0337,Tetramethyl lead,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26931,T3D0337,Tetramethyl lead,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26932,T3D0338,Tetraethyl lead,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26933,T3D0338,Tetraethyl lead,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26934,T3D0338,Tetraethyl lead,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26935,T3D0338,Tetraethyl lead,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26936,T3D0338,Tetraethyl lead,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26937,T3D1322,Lead chlorate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
26938,T3D1322,Lead chlorate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes inproper activation, altering proper functioning of cAMP messenger pathways. (R061)"
26939,T3D1322,Lead chlorate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
26940,T3D1322,Lead chlorate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
26941,T3D1322,Lead chlorate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26942,T3D1322,Lead chlorate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26943,T3D1322,Lead chlorate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26944,T3D1322,Lead chlorate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26945,T3D1322,Lead chlorate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26946,T3D1322,Lead chlorate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26947,T3D1322,Lead chlorate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26948,T3D1322,Lead chlorate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26949,T3D1322,Lead chlorate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26950,T3D1322,Lead chlorate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26951,T3D1322,Lead chlorate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26952,T3D1322,Lead chlorate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26953,T3D1322,Lead chlorate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26954,T3D1322,Lead chlorate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26955,T3D1322,Lead chlorate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26956,T3D1322,Lead chlorate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26957,T3D1322,Lead chlorate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
26958,T3D1322,Lead chlorate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
26959,T3D1322,Lead chlorate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
26960,T3D1322,Lead chlorate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
26961,T3D1322,Lead chlorate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26962,T3D1322,Lead chlorate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
26963,T3D1322,Lead chlorate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
26964,T3D1322,Lead chlorate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
26965,T3D1322,Lead chlorate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
26966,T3D1323,Lead oxalate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
26967,T3D1323,Lead oxalate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
26968,T3D1323,Lead oxalate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
26969,T3D1323,Lead oxalate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
26970,T3D1323,Lead oxalate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26971,T3D1323,Lead oxalate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26972,T3D1323,Lead oxalate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26973,T3D1323,Lead oxalate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26974,T3D1323,Lead oxalate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26975,T3D1323,Lead oxalate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26976,T3D1323,Lead oxalate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
26977,T3D1323,Lead oxalate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26978,T3D1323,Lead oxalate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26979,T3D1323,Lead oxalate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26980,T3D1323,Lead oxalate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26981,T3D1323,Lead oxalate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26982,T3D1323,Lead oxalate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26983,T3D1323,Lead oxalate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26984,T3D1323,Lead oxalate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26985,T3D1323,Lead oxalate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
26986,T3D1323,Lead oxalate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
26987,T3D1323,Lead oxalate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
26988,T3D1323,Lead oxalate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
26989,T3D1323,Lead oxalate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
26990,T3D1323,Lead oxalate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
26991,T3D1323,Lead oxalate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
26992,T3D1323,Lead oxalate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
26993,T3D1323,Lead oxalate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
26994,T3D1323,Lead oxalate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
26995,T3D1324,Lead stearate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
26996,T3D1324,Lead stearate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
26997,T3D1324,Lead stearate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
26998,T3D1324,Lead stearate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
26999,T3D1324,Lead stearate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27000,T3D1324,Lead stearate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27001,T3D1324,Lead stearate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27002,T3D1324,Lead stearate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27003,T3D1324,Lead stearate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27004,T3D1324,Lead stearate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27005,T3D1324,Lead stearate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27006,T3D1324,Lead stearate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27007,T3D1324,Lead stearate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27008,T3D1324,Lead stearate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27009,T3D1324,Lead stearate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27010,T3D1324,Lead stearate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27011,T3D1324,Lead stearate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27012,T3D1324,Lead stearate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27013,T3D1324,Lead stearate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27014,T3D1324,Lead stearate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27015,T3D1324,Lead stearate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27016,T3D1324,Lead stearate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27017,T3D1324,Lead stearate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27018,T3D1324,Lead stearate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27019,T3D1324,Lead stearate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27020,T3D1324,Lead stearate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27021,T3D1324,Lead stearate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27022,T3D1324,Lead stearate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27023,T3D1324,Lead stearate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27024,T3D1325,Lead selenide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27025,T3D1325,Lead selenide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27026,T3D1325,Lead selenide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27027,T3D1325,Lead selenide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27028,T3D1325,Lead selenide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27029,T3D1325,Lead selenide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27030,T3D1325,Lead selenide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27031,T3D1325,Lead selenide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27032,T3D1325,Lead selenide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27033,T3D1325,Lead selenide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27034,T3D1325,Lead selenide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27035,T3D1325,Lead selenide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27036,T3D1325,Lead selenide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27037,T3D1325,Lead selenide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27038,T3D1325,Lead selenide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27039,T3D1325,Lead selenide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27040,T3D1325,Lead selenide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27041,T3D1325,Lead selenide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27042,T3D1325,Lead selenide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27043,T3D1325,Lead selenide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27044,T3D1325,Lead selenide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27045,T3D1325,Lead selenide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27046,T3D1325,Lead selenide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27047,T3D1325,Lead selenide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27048,T3D1325,Lead selenide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27049,T3D1325,Lead selenide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27050,T3D1325,Lead selenide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27051,T3D1325,Lead selenide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27052,T3D1325,Lead selenide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27053,T3D1326,Lead telluride,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27054,T3D1326,Lead telluride,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27055,T3D1326,Lead telluride,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27056,T3D1326,Lead telluride,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27057,T3D1326,Lead telluride,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27058,T3D1326,Lead telluride,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27059,T3D1326,Lead telluride,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27060,T3D1326,Lead telluride,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27061,T3D1326,Lead telluride,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27062,T3D1326,Lead telluride,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27063,T3D1326,Lead telluride,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27064,T3D1326,Lead telluride,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27065,T3D1326,Lead telluride,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27066,T3D1326,Lead telluride,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27067,T3D1326,Lead telluride,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27068,T3D1326,Lead telluride,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27069,T3D1326,Lead telluride,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27070,T3D1326,Lead telluride,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27071,T3D1326,Lead telluride,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27072,T3D1326,Lead telluride,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27073,T3D1326,Lead telluride,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27074,T3D1326,Lead telluride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27075,T3D1326,Lead telluride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27076,T3D1326,Lead telluride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27077,T3D1326,Lead telluride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27078,T3D1326,Lead telluride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27079,T3D1326,Lead telluride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27080,T3D1326,Lead telluride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27081,T3D1326,Lead telluride,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27082,T3D1327,Lead fluoride,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27083,T3D1327,Lead fluoride,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27084,T3D1327,Lead fluoride,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27085,T3D1327,Lead fluoride,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27086,T3D1327,Lead fluoride,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27087,T3D1327,Lead fluoride,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27088,T3D1327,Lead fluoride,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27089,T3D1327,Lead fluoride,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27090,T3D1327,Lead fluoride,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27091,T3D1327,Lead fluoride,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27092,T3D1327,Lead fluoride,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27093,T3D1327,Lead fluoride,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27094,T3D1327,Lead fluoride,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27095,T3D1327,Lead fluoride,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27096,T3D1327,Lead fluoride,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27097,T3D1327,Lead fluoride,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27098,T3D1327,Lead fluoride,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27099,T3D1327,Lead fluoride,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27100,T3D1327,Lead fluoride,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27101,T3D1327,Lead fluoride,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27102,T3D1327,Lead fluoride,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27103,T3D1327,Lead fluoride,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27104,T3D1327,Lead fluoride,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27105,T3D1327,Lead fluoride,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27106,T3D1327,Lead fluoride,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27107,T3D1327,Lead fluoride,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27108,T3D1327,Lead fluoride,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27109,T3D1327,Lead fluoride,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27110,T3D1327,Lead fluoride,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27111,T3D1328,Lead hydroxide,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27112,T3D1328,Lead hydroxide,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27113,T3D1328,Lead hydroxide,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27114,T3D1328,Lead hydroxide,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27115,T3D1328,Lead hydroxide,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27116,T3D1328,Lead hydroxide,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27117,T3D1328,Lead hydroxide,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27118,T3D1328,Lead hydroxide,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27119,T3D1328,Lead hydroxide,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27120,T3D1328,Lead hydroxide,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27121,T3D1328,Lead hydroxide,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27122,T3D1328,Lead hydroxide,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27123,T3D1328,Lead hydroxide,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27124,T3D1328,Lead hydroxide,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27125,T3D1328,Lead hydroxide,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27126,T3D1328,Lead hydroxide,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27127,T3D1328,Lead hydroxide,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27128,T3D1328,Lead hydroxide,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27129,T3D1328,Lead hydroxide,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27130,T3D1328,Lead hydroxide,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27131,T3D1328,Lead hydroxide,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27132,T3D1328,Lead hydroxide,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27133,T3D1328,Lead hydroxide,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27134,T3D1328,Lead hydroxide,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27135,T3D1328,Lead hydroxide,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27136,T3D1328,Lead hydroxide,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27137,T3D1328,Lead hydroxide,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27138,T3D1328,Lead hydroxide,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27139,T3D1328,Lead hydroxide,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27140,T3D1329,Plumbane,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27141,T3D1329,Plumbane,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27142,T3D1329,Plumbane,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27143,T3D1329,Plumbane,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27144,T3D1329,Plumbane,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27145,T3D1329,Plumbane,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27146,T3D1329,Plumbane,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27147,T3D1329,Plumbane,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27148,T3D1329,Plumbane,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27149,T3D1329,Plumbane,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27150,T3D1329,Plumbane,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27151,T3D1329,Plumbane,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27152,T3D1329,Plumbane,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27153,T3D1329,Plumbane,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27154,T3D1329,Plumbane,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27155,T3D1329,Plumbane,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27156,T3D1329,Plumbane,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27157,T3D1329,Plumbane,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27158,T3D1329,Plumbane,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27159,T3D1329,Plumbane,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27160,T3D1329,Plumbane,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27161,T3D1329,Plumbane,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27162,T3D1329,Plumbane,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27163,T3D1329,Plumbane,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27164,T3D1329,Plumbane,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27165,T3D1329,Plumbane,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27166,T3D1329,Plumbane,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27167,T3D1329,Plumbane,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27168,T3D1329,Plumbane,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27169,T3D1330,Basic lead carbonate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27170,T3D1330,Basic lead carbonate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27171,T3D1330,Basic lead carbonate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27172,T3D1330,Basic lead carbonate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27173,T3D1330,Basic lead carbonate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27174,T3D1330,Basic lead carbonate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27175,T3D1330,Basic lead carbonate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27176,T3D1330,Basic lead carbonate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27177,T3D1330,Basic lead carbonate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27178,T3D1330,Basic lead carbonate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27179,T3D1330,Basic lead carbonate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27180,T3D1330,Basic lead carbonate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27181,T3D1330,Basic lead carbonate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27182,T3D1330,Basic lead carbonate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27183,T3D1330,Basic lead carbonate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27184,T3D1330,Basic lead carbonate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27185,T3D1330,Basic lead carbonate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27186,T3D1330,Basic lead carbonate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27187,T3D1330,Basic lead carbonate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27188,T3D1330,Basic lead carbonate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27189,T3D1330,Basic lead carbonate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27190,T3D1330,Basic lead carbonate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27191,T3D1330,Basic lead carbonate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27192,T3D1330,Basic lead carbonate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27193,T3D1330,Basic lead carbonate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27194,T3D1330,Basic lead carbonate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27195,T3D1330,Basic lead carbonate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27196,T3D1330,Basic lead carbonate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27197,T3D1330,Basic lead carbonate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27198,T3D1331,Lead subacetate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27199,T3D1331,Lead subacetate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27200,T3D1331,Lead subacetate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27201,T3D1331,Lead subacetate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27202,T3D1331,Lead subacetate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27203,T3D1331,Lead subacetate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27204,T3D1331,Lead subacetate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27205,T3D1331,Lead subacetate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27206,T3D1331,Lead subacetate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27207,T3D1331,Lead subacetate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27208,T3D1331,Lead subacetate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27209,T3D1331,Lead subacetate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27210,T3D1331,Lead subacetate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27211,T3D1331,Lead subacetate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27212,T3D1331,Lead subacetate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27213,T3D1331,Lead subacetate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27214,T3D1331,Lead subacetate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27215,T3D1331,Lead subacetate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27216,T3D1331,Lead subacetate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27217,T3D1331,Lead subacetate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27218,T3D1331,Lead subacetate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27219,T3D1331,Lead subacetate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27220,T3D1331,Lead subacetate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27221,T3D1331,Lead subacetate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27222,T3D1331,Lead subacetate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27223,T3D1331,Lead subacetate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27224,T3D1331,Lead subacetate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27225,T3D1331,Lead subacetate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27226,T3D1331,Lead subacetate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27227,T3D1332,Lead tetraacetate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27228,T3D1332,Lead tetraacetate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27229,T3D1332,Lead tetraacetate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27230,T3D1332,Lead tetraacetate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27231,T3D1332,Lead tetraacetate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27232,T3D1332,Lead tetraacetate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27233,T3D1332,Lead tetraacetate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27234,T3D1332,Lead tetraacetate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27235,T3D1332,Lead tetraacetate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27236,T3D1332,Lead tetraacetate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27237,T3D1332,Lead tetraacetate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27238,T3D1332,Lead tetraacetate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27239,T3D1332,Lead tetraacetate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27240,T3D1332,Lead tetraacetate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27241,T3D1332,Lead tetraacetate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27242,T3D1332,Lead tetraacetate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27243,T3D1332,Lead tetraacetate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27244,T3D1332,Lead tetraacetate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27245,T3D1332,Lead tetraacetate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27246,T3D1332,Lead tetraacetate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27247,T3D1332,Lead tetraacetate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27248,T3D1332,Lead tetraacetate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27249,T3D1332,Lead tetraacetate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27250,T3D1332,Lead tetraacetate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27251,T3D1332,Lead tetraacetate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27252,T3D1332,Lead tetraacetate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27253,T3D1332,Lead tetraacetate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27254,T3D1332,Lead tetraacetate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27255,T3D1332,Lead tetraacetate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27256,T3D1333,Lead tungstate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27257,T3D1333,Lead tungstate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27258,T3D1333,Lead tungstate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27259,T3D1333,Lead tungstate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27260,T3D1333,Lead tungstate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27261,T3D1333,Lead tungstate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27262,T3D1333,Lead tungstate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27263,T3D1333,Lead tungstate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27264,T3D1333,Lead tungstate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27265,T3D1333,Lead tungstate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27266,T3D1333,Lead tungstate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27267,T3D1333,Lead tungstate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27268,T3D1333,Lead tungstate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27269,T3D1333,Lead tungstate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27270,T3D1333,Lead tungstate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27271,T3D1333,Lead tungstate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27272,T3D1333,Lead tungstate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27273,T3D1333,Lead tungstate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27274,T3D1333,Lead tungstate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27275,T3D1333,Lead tungstate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27276,T3D1333,Lead tungstate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27277,T3D1333,Lead tungstate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27278,T3D1333,Lead tungstate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27279,T3D1333,Lead tungstate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27280,T3D1333,Lead tungstate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27281,T3D1333,Lead tungstate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27282,T3D1333,Lead tungstate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27283,T3D1333,Lead tungstate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27284,T3D1333,Lead tungstate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27285,T3D1334,Lead thiosulfate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27286,T3D1334,Lead thiosulfate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27287,T3D1334,Lead thiosulfate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27288,T3D1334,Lead thiosulfate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27289,T3D1334,Lead thiosulfate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27290,T3D1334,Lead thiosulfate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27291,T3D1334,Lead thiosulfate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27292,T3D1334,Lead thiosulfate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27293,T3D1334,Lead thiosulfate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27294,T3D1334,Lead thiosulfate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27295,T3D1334,Lead thiosulfate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27296,T3D1334,Lead thiosulfate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27297,T3D1334,Lead thiosulfate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27298,T3D1334,Lead thiosulfate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27299,T3D1334,Lead thiosulfate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27300,T3D1334,Lead thiosulfate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27301,T3D1334,Lead thiosulfate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27302,T3D1334,Lead thiosulfate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27303,T3D1334,Lead thiosulfate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27304,T3D1334,Lead thiosulfate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27305,T3D1334,Lead thiosulfate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27306,T3D1334,Lead thiosulfate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27307,T3D1334,Lead thiosulfate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27308,T3D1334,Lead thiosulfate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27309,T3D1334,Lead thiosulfate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27310,T3D1334,Lead thiosulfate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27311,T3D1334,Lead thiosulfate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27312,T3D1334,Lead thiosulfate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27313,T3D1334,Lead thiosulfate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27314,T3D1335,Lead perchlorate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27315,T3D1335,Lead perchlorate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27316,T3D1335,Lead perchlorate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27317,T3D1335,Lead perchlorate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27318,T3D1335,Lead perchlorate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27319,T3D1335,Lead perchlorate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27320,T3D1335,Lead perchlorate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27321,T3D1335,Lead perchlorate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27322,T3D1335,Lead perchlorate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27323,T3D1335,Lead perchlorate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27324,T3D1335,Lead perchlorate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27325,T3D1335,Lead perchlorate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27326,T3D1335,Lead perchlorate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27327,T3D1335,Lead perchlorate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27328,T3D1335,Lead perchlorate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27329,T3D1335,Lead perchlorate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27330,T3D1335,Lead perchlorate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27331,T3D1335,Lead perchlorate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27332,T3D1335,Lead perchlorate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27333,T3D1335,Lead perchlorate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27334,T3D1335,Lead perchlorate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27335,T3D1335,Lead perchlorate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27336,T3D1335,Lead perchlorate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27337,T3D1335,Lead perchlorate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27338,T3D1335,Lead perchlorate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27339,T3D1335,Lead perchlorate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27340,T3D1335,Lead perchlorate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27341,T3D1335,Lead perchlorate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27342,T3D1335,Lead perchlorate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27343,T3D1336,Lead acetate trihydrate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27344,T3D1336,Lead acetate trihydrate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27345,T3D1336,Lead acetate trihydrate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27346,T3D1336,Lead acetate trihydrate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27347,T3D1336,Lead acetate trihydrate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27348,T3D1336,Lead acetate trihydrate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27349,T3D1336,Lead acetate trihydrate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27350,T3D1336,Lead acetate trihydrate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27351,T3D1336,Lead acetate trihydrate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27352,T3D1336,Lead acetate trihydrate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27353,T3D1336,Lead acetate trihydrate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27354,T3D1336,Lead acetate trihydrate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27355,T3D1336,Lead acetate trihydrate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27356,T3D1336,Lead acetate trihydrate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27357,T3D1336,Lead acetate trihydrate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27358,T3D1336,Lead acetate trihydrate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27359,T3D1336,Lead acetate trihydrate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27360,T3D1336,Lead acetate trihydrate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27361,T3D1336,Lead acetate trihydrate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27362,T3D1336,Lead acetate trihydrate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27363,T3D1336,Lead acetate trihydrate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27364,T3D1336,Lead acetate trihydrate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27365,T3D1336,Lead acetate trihydrate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27366,T3D1336,Lead acetate trihydrate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27367,T3D1336,Lead acetate trihydrate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27368,T3D1336,Lead acetate trihydrate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27369,T3D1336,Lead acetate trihydrate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27370,T3D1336,Lead acetate trihydrate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27371,T3D1336,Lead acetate trihydrate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27372,T3D1337,Basic lead acetate,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27373,T3D1337,Basic lead acetate,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27374,T3D1337,Basic lead acetate,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27375,T3D1337,Basic lead acetate,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27376,T3D1337,Basic lead acetate,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27377,T3D1337,Basic lead acetate,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27378,T3D1337,Basic lead acetate,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27379,T3D1337,Basic lead acetate,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27380,T3D1337,Basic lead acetate,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27381,T3D1337,Basic lead acetate,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27382,T3D1337,Basic lead acetate,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27383,T3D1337,Basic lead acetate,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27384,T3D1337,Basic lead acetate,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27385,T3D1337,Basic lead acetate,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27386,T3D1337,Basic lead acetate,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27387,T3D1337,Basic lead acetate,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27388,T3D1337,Basic lead acetate,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27389,T3D1337,Basic lead acetate,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27390,T3D1337,Basic lead acetate,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27391,T3D1337,Basic lead acetate,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27392,T3D1337,Basic lead acetate,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27393,T3D1337,Basic lead acetate,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27394,T3D1337,Basic lead acetate,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27395,T3D1337,Basic lead acetate,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27396,T3D1337,Basic lead acetate,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27397,T3D1337,Basic lead acetate,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27398,T3D1337,Basic lead acetate,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27399,T3D1337,Basic lead acetate,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27400,T3D1337,Basic lead acetate,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27401,T3D1338,Diethyldimethyl lead,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27402,T3D1338,Diethyldimethyl lead,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27403,T3D1338,Diethyldimethyl lead,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27404,T3D1338,Diethyldimethyl lead,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27405,T3D1338,Diethyldimethyl lead,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27406,T3D1338,Diethyldimethyl lead,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27407,T3D1338,Diethyldimethyl lead,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27408,T3D1338,Diethyldimethyl lead,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27409,T3D1338,Diethyldimethyl lead,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27410,T3D1338,Diethyldimethyl lead,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27411,T3D1338,Diethyldimethyl lead,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27412,T3D1338,Diethyldimethyl lead,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27413,T3D1338,Diethyldimethyl lead,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27414,T3D1338,Diethyldimethyl lead,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27415,T3D1338,Diethyldimethyl lead,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27416,T3D1338,Diethyldimethyl lead,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27417,T3D1338,Diethyldimethyl lead,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27418,T3D1338,Diethyldimethyl lead,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27419,T3D1338,Diethyldimethyl lead,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27420,T3D1338,Diethyldimethyl lead,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27421,T3D1338,Diethyldimethyl lead,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27422,T3D1338,Diethyldimethyl lead,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27423,T3D1338,Diethyldimethyl lead,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27424,T3D1338,Diethyldimethyl lead,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27425,T3D1338,Diethyldimethyl lead,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27426,T3D1338,Diethyldimethyl lead,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27427,T3D1338,Diethyldimethyl lead,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27428,T3D1338,Diethyldimethyl lead,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27429,T3D1338,Diethyldimethyl lead,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27430,T3D1339,Methyltriethyl lead,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27431,T3D1339,Methyltriethyl lead,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27432,T3D1339,Methyltriethyl lead,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27433,T3D1339,Methyltriethyl lead,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27434,T3D1339,Methyltriethyl lead,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27435,T3D1339,Methyltriethyl lead,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27436,T3D1339,Methyltriethyl lead,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27437,T3D1339,Methyltriethyl lead,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27438,T3D1339,Methyltriethyl lead,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27439,T3D1339,Methyltriethyl lead,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27440,T3D1339,Methyltriethyl lead,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27441,T3D1339,Methyltriethyl lead,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27442,T3D1339,Methyltriethyl lead,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27443,T3D1339,Methyltriethyl lead,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27444,T3D1339,Methyltriethyl lead,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27445,T3D1339,Methyltriethyl lead,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27446,T3D1339,Methyltriethyl lead,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27447,T3D1339,Methyltriethyl lead,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27448,T3D1339,Methyltriethyl lead,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27449,T3D1339,Methyltriethyl lead,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27450,T3D1339,Methyltriethyl lead,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27451,T3D1339,Methyltriethyl lead,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27452,T3D1339,Methyltriethyl lead,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27453,T3D1339,Methyltriethyl lead,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27454,T3D1339,Methyltriethyl lead,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27455,T3D1339,Methyltriethyl lead,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27456,T3D1339,Methyltriethyl lead,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27457,T3D1339,Methyltriethyl lead,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27458,T3D1339,Methyltriethyl lead,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27459,T3D1340,Ethyltrimethyl lead,Acyl-CoA-binding protein,P07108,"Lead is known to bind ACBP, which is responsible for the regulation of various processes such as acyl-CoA metabolism, GABA-A/benzodiazepine receptor modulation, steroidogenesis, intestinal cholecystokinin release, and insulin secretion. (R062)"
27460,T3D1340,Ethyltrimethyl lead,Calmodulin,P62158,"Lead has been shown to competitively inhibit calcium's binding of calmodulin, interfering with neurotransmitter release. Lead binding of calmodulin causes improper activation, altering proper functioning of cAMP messenger pathways. (R061)"
27461,T3D1340,Ethyltrimethyl lead,Delta-aminolevulinic acid dehydratase,P13716,"Lead inhibition of ALAD prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27462,T3D1340,Ethyltrimethyl lead,"Ferrochelatase, mitochondrial",P22830,"Lead inhibition of ferrochelatase prevents the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (R056)"
27463,T3D1340,Ethyltrimethyl lead,Glutamate [NMDA] receptor subunit 3A,Q8TCU5,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27464,T3D1340,Ethyltrimethyl lead,Glutamate [NMDA] receptor subunit 3B,O60391,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27465,T3D1340,Ethyltrimethyl lead,Glutamate [NMDA] receptor subunit epsilon-1,Q12879,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27466,T3D1340,Ethyltrimethyl lead,Glutamate [NMDA] receptor subunit epsilon-2,Q13224,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27467,T3D1340,Ethyltrimethyl lead,Glutamate [NMDA] receptor subunit epsilon-3,Q14957,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27468,T3D1340,Ethyltrimethyl lead,Glutamate [NMDA] receptor subunit epsilon-4,O15399,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27469,T3D1340,Ethyltrimethyl lead,Glutamate [NMDA] receptor subunit zeta-1,Q05586,"Lead exhibits competitive inhibition at the NMDA receptor, affecting neurotransmitter release. (R063)"
27470,T3D1340,Ethyltrimethyl lead,Protein kinase C alpha type,P17252,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27471,T3D1340,Ethyltrimethyl lead,Protein kinase C beta type,P05771,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27472,T3D1340,Ethyltrimethyl lead,Protein kinase C delta type,Q05655,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27473,T3D1340,Ethyltrimethyl lead,Protein kinase C epsilon type,Q02156,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27474,T3D1340,Ethyltrimethyl lead,Protein kinase C eta type,P24723,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27475,T3D1340,Ethyltrimethyl lead,Protein kinase C gamma type,P05129,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27476,T3D1340,Ethyltrimethyl lead,Protein kinase C iota type,P41743,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27477,T3D1340,Ethyltrimethyl lead,Protein kinase C theta type,Q04759,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27478,T3D1340,Ethyltrimethyl lead,Protein kinase C zeta type,Q05513,"Lead exhibits competitive inhibition with calcium at protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R266)"
27479,T3D1340,Ethyltrimethyl lead,Sodium/potassium-transporting ATPase gamma chain,P54710,Lead binds to sodium/potassium-transporting ATPases. (R065)
27480,T3D1340,Ethyltrimethyl lead,Sodium/potassium-transporting ATPase alpha-1 chain,P05023,Lead binds to sodium/potassium-transporting ATPases. (R065)
27481,T3D1340,Ethyltrimethyl lead,Sodium/potassium-transporting ATPase subunit alpha-2,P50993,Lead binds to sodium/potassium-transporting ATPases. (R065)
27482,T3D1340,Ethyltrimethyl lead,Sodium/potassium-transporting ATPase subunit alpha-3,P13637,Lead binds to sodium/potassium-transporting ATPases. (R065)
27483,T3D1340,Ethyltrimethyl lead,Sodium/potassium-transporting ATPase subunit alpha-4,Q13733,Lead binds to sodium/potassium-transporting ATPases. (R065)
27484,T3D1340,Ethyltrimethyl lead,Sodium/potassium-transporting ATPase subunit beta-1,P05026,Lead binds to sodium/potassium-transporting ATPases. (R065)
27485,T3D1340,Ethyltrimethyl lead,Sodium/potassium-transporting ATPase subunit beta-2,P14415,Lead binds to sodium/potassium-transporting ATPases. (R065)
27486,T3D1340,Ethyltrimethyl lead,Sodium/potassium-transporting ATPase subunit beta-3,P54709,Lead binds to sodium/potassium-transporting ATPases. (R065)
27487,T3D1340,Ethyltrimethyl lead,Thymosin beta-4,P62328,"Lead has been shown to bind thymosin beta-4, which functions in the modulation of cytoskeletion, stimulation of CaM-dependent kinases, and GABA-A receptor complex function. It is also an immunotransmitter. (R062)"
27488,T3D0341,Mercury(II) sulfide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27489,T3D0341,Mercury(II) sulfide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27490,T3D0341,Mercury(II) sulfide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27491,T3D0341,Mercury(II) sulfide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27492,T3D0341,Mercury(II) sulfide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27493,T3D0341,Mercury(II) sulfide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27494,T3D0341,Mercury(II) sulfide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27495,T3D0341,Mercury(II) sulfide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27496,T3D0341,Mercury(II) sulfide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27497,T3D0341,Mercury(II) sulfide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27498,T3D0341,Mercury(II) sulfide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27499,T3D0341,Mercury(II) sulfide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27500,T3D0341,Mercury(II) sulfide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27501,T3D0341,Mercury(II) sulfide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27502,T3D0341,Mercury(II) sulfide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27503,T3D0341,Mercury(II) sulfide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27504,T3D0341,Mercury(II) sulfide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27505,T3D0341,Mercury(II) sulfide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27506,T3D0341,Mercury(II) sulfide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27507,T3D0341,Mercury(II) sulfide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27508,T3D0341,Mercury(II) sulfide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27509,T3D0341,Mercury(II) sulfide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27510,T3D0341,Mercury(II) sulfide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27511,T3D0341,Mercury(II) sulfide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27512,T3D0341,Mercury(II) sulfide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27513,T3D0341,Mercury(II) sulfide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27514,T3D0341,Mercury(II) sulfide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27515,T3D0341,Mercury(II) sulfide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27516,T3D0341,Mercury(II) sulfide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27517,T3D0341,Mercury(II) sulfide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27518,T3D0342,Mercury(II) oxide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27519,T3D0342,Mercury(II) oxide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27520,T3D0342,Mercury(II) oxide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27521,T3D0342,Mercury(II) oxide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27522,T3D0342,Mercury(II) oxide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27523,T3D0342,Mercury(II) oxide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27524,T3D0342,Mercury(II) oxide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27525,T3D0342,Mercury(II) oxide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27526,T3D0342,Mercury(II) oxide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27527,T3D0342,Mercury(II) oxide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27528,T3D0342,Mercury(II) oxide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27529,T3D0342,Mercury(II) oxide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27530,T3D0342,Mercury(II) oxide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27531,T3D0342,Mercury(II) oxide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27532,T3D0342,Mercury(II) oxide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27533,T3D0342,Mercury(II) oxide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27534,T3D0342,Mercury(II) oxide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27535,T3D0342,Mercury(II) oxide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27536,T3D0342,Mercury(II) oxide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27537,T3D0342,Mercury(II) oxide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27538,T3D0342,Mercury(II) oxide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27539,T3D0342,Mercury(II) oxide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27540,T3D0342,Mercury(II) oxide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27541,T3D0342,Mercury(II) oxide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27542,T3D0342,Mercury(II) oxide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27543,T3D0342,Mercury(II) oxide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27544,T3D0342,Mercury(II) oxide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27545,T3D0342,Mercury(II) oxide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27546,T3D0342,Mercury(II) oxide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27547,T3D0342,Mercury(II) oxide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27548,T3D0343,Mercury(I) chloride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27549,T3D0343,Mercury(I) chloride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27550,T3D0343,Mercury(I) chloride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27551,T3D0343,Mercury(I) chloride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27552,T3D0343,Mercury(I) chloride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27553,T3D0343,Mercury(I) chloride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27554,T3D0343,Mercury(I) chloride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27555,T3D0343,Mercury(I) chloride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27556,T3D0343,Mercury(I) chloride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27557,T3D0343,Mercury(I) chloride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27558,T3D0343,Mercury(I) chloride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27559,T3D0343,Mercury(I) chloride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27560,T3D0343,Mercury(I) chloride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27561,T3D0343,Mercury(I) chloride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27562,T3D0343,Mercury(I) chloride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27563,T3D0343,Mercury(I) chloride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27564,T3D0343,Mercury(I) chloride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27565,T3D0343,Mercury(I) chloride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27566,T3D0343,Mercury(I) chloride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27567,T3D0343,Mercury(I) chloride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27568,T3D0343,Mercury(I) chloride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27569,T3D0343,Mercury(I) chloride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27570,T3D0343,Mercury(I) chloride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27571,T3D0343,Mercury(I) chloride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27572,T3D0343,Mercury(I) chloride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27573,T3D0343,Mercury(I) chloride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27574,T3D0343,Mercury(I) chloride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27575,T3D0343,Mercury(I) chloride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27576,T3D0343,Mercury(I) chloride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27577,T3D0344,Phenylmercuric acetate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27578,T3D0344,Phenylmercuric acetate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27579,T3D0344,Phenylmercuric acetate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27580,T3D0344,Phenylmercuric acetate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27581,T3D0344,Phenylmercuric acetate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27582,T3D0344,Phenylmercuric acetate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27583,T3D0344,Phenylmercuric acetate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27584,T3D0344,Phenylmercuric acetate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27585,T3D0344,Phenylmercuric acetate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27586,T3D0344,Phenylmercuric acetate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27587,T3D0344,Phenylmercuric acetate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27588,T3D0344,Phenylmercuric acetate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27589,T3D0344,Phenylmercuric acetate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27590,T3D0344,Phenylmercuric acetate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27591,T3D0344,Phenylmercuric acetate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27592,T3D0344,Phenylmercuric acetate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27593,T3D0344,Phenylmercuric acetate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27594,T3D0344,Phenylmercuric acetate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27595,T3D0344,Phenylmercuric acetate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27596,T3D0344,Phenylmercuric acetate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27597,T3D0344,Phenylmercuric acetate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27598,T3D0344,Phenylmercuric acetate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27599,T3D0344,Phenylmercuric acetate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27600,T3D0344,Phenylmercuric acetate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27601,T3D0344,Phenylmercuric acetate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27602,T3D0344,Phenylmercuric acetate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27603,T3D0344,Phenylmercuric acetate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27604,T3D0344,Phenylmercuric acetate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27605,T3D0344,Phenylmercuric acetate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27606,T3D0344,Phenylmercuric acetate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27607,T3D0345,Mercury selenide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27608,T3D0345,Mercury selenide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27609,T3D0345,Mercury selenide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27610,T3D0345,Mercury selenide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27611,T3D0345,Mercury selenide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27612,T3D0345,Mercury selenide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27613,T3D0345,Mercury selenide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27614,T3D0345,Mercury selenide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27615,T3D0345,Mercury selenide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27616,T3D0345,Mercury selenide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27617,T3D0345,Mercury selenide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27618,T3D0345,Mercury selenide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27619,T3D0345,Mercury selenide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27620,T3D0345,Mercury selenide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27621,T3D0345,Mercury selenide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27622,T3D0345,Mercury selenide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27623,T3D0345,Mercury selenide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27624,T3D0345,Mercury selenide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27625,T3D0345,Mercury selenide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27626,T3D0345,Mercury selenide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27627,T3D0345,Mercury selenide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27628,T3D0345,Mercury selenide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27629,T3D0345,Mercury selenide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27630,T3D0345,Mercury selenide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27631,T3D0345,Mercury selenide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27632,T3D0345,Mercury selenide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27633,T3D0345,Mercury selenide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27634,T3D0345,Mercury selenide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27635,T3D0345,Mercury selenide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27636,T3D0346,Mercury telluride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27637,T3D0346,Mercury telluride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27638,T3D0346,Mercury telluride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27639,T3D0346,Mercury telluride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27640,T3D0346,Mercury telluride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27641,T3D0346,Mercury telluride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27642,T3D0346,Mercury telluride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27643,T3D0346,Mercury telluride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27644,T3D0346,Mercury telluride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27645,T3D0346,Mercury telluride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27646,T3D0346,Mercury telluride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27647,T3D0346,Mercury telluride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27648,T3D0346,Mercury telluride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27649,T3D0346,Mercury telluride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27650,T3D0346,Mercury telluride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27651,T3D0346,Mercury telluride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27652,T3D0346,Mercury telluride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27653,T3D0346,Mercury telluride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27654,T3D0346,Mercury telluride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27655,T3D0346,Mercury telluride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27656,T3D0346,Mercury telluride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27657,T3D0346,Mercury telluride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27658,T3D0346,Mercury telluride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27659,T3D0346,Mercury telluride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27660,T3D0346,Mercury telluride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27661,T3D0346,Mercury telluride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27662,T3D0346,Mercury telluride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27663,T3D0346,Mercury telluride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27664,T3D0346,Mercury telluride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27665,T3D0346,Mercury telluride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27666,T3D0347,Mercury cadmium telluride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27667,T3D0347,Mercury cadmium telluride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27668,T3D0347,Mercury cadmium telluride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27669,T3D0347,Mercury cadmium telluride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27670,T3D0347,Mercury cadmium telluride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27671,T3D0347,Mercury cadmium telluride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27672,T3D0347,Mercury cadmium telluride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27673,T3D0347,Mercury cadmium telluride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27674,T3D0347,Mercury cadmium telluride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27675,T3D0347,Mercury cadmium telluride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27676,T3D0347,Mercury cadmium telluride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27677,T3D0347,Mercury cadmium telluride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27678,T3D0347,Mercury cadmium telluride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27679,T3D0347,Mercury cadmium telluride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27680,T3D0347,Mercury cadmium telluride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27681,T3D0347,Mercury cadmium telluride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27682,T3D0347,Mercury cadmium telluride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27683,T3D0347,Mercury cadmium telluride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27684,T3D0347,Mercury cadmium telluride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27685,T3D0347,Mercury cadmium telluride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27686,T3D0347,Mercury cadmium telluride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27687,T3D0347,Mercury cadmium telluride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27688,T3D0347,Mercury cadmium telluride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27689,T3D0347,Mercury cadmium telluride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27690,T3D0347,Mercury cadmium telluride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27691,T3D0347,Mercury cadmium telluride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27692,T3D0347,Mercury cadmium telluride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27693,T3D0347,Mercury cadmium telluride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27694,T3D0347,Mercury cadmium telluride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27695,T3D0347,Mercury cadmium telluride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27696,T3D0348,Mercury(II) acetate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27697,T3D0348,Mercury(II) acetate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27698,T3D0348,Mercury(II) acetate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27699,T3D0348,Mercury(II) acetate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27700,T3D0348,Mercury(II) acetate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27701,T3D0348,Mercury(II) acetate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27702,T3D0348,Mercury(II) acetate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27703,T3D0348,Mercury(II) acetate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27704,T3D0348,Mercury(II) acetate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27705,T3D0348,Mercury(II) acetate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27706,T3D0348,Mercury(II) acetate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27707,T3D0348,Mercury(II) acetate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27708,T3D0348,Mercury(II) acetate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27709,T3D0348,Mercury(II) acetate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27710,T3D0348,Mercury(II) acetate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27711,T3D0348,Mercury(II) acetate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27712,T3D0348,Mercury(II) acetate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27713,T3D0348,Mercury(II) acetate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27714,T3D0348,Mercury(II) acetate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27715,T3D0348,Mercury(II) acetate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27716,T3D0348,Mercury(II) acetate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27717,T3D0348,Mercury(II) acetate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27718,T3D0348,Mercury(II) acetate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27719,T3D0348,Mercury(II) acetate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27720,T3D0348,Mercury(II) acetate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27721,T3D0348,Mercury(II) acetate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27722,T3D0348,Mercury(II) acetate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27723,T3D0348,Mercury(II) acetate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27724,T3D0348,Mercury(II) acetate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27725,T3D0349,Mercury(I) acetate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27726,T3D0349,Mercury(I) acetate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27727,T3D0349,Mercury(I) acetate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27728,T3D0349,Mercury(I) acetate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27729,T3D0349,Mercury(I) acetate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27730,T3D0349,Mercury(I) acetate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27731,T3D0349,Mercury(I) acetate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27732,T3D0349,Mercury(I) acetate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27733,T3D0349,Mercury(I) acetate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27734,T3D0349,Mercury(I) acetate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27735,T3D0349,Mercury(I) acetate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27736,T3D0349,Mercury(I) acetate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27737,T3D0349,Mercury(I) acetate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27738,T3D0349,Mercury(I) acetate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27739,T3D0349,Mercury(I) acetate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27740,T3D0349,Mercury(I) acetate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27741,T3D0349,Mercury(I) acetate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27742,T3D0349,Mercury(I) acetate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27743,T3D0349,Mercury(I) acetate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27744,T3D0349,Mercury(I) acetate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27745,T3D0349,Mercury(I) acetate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27746,T3D0349,Mercury(I) acetate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27747,T3D0349,Mercury(I) acetate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27748,T3D0349,Mercury(I) acetate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27749,T3D0349,Mercury(I) acetate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27750,T3D0349,Mercury(I) acetate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27751,T3D0349,Mercury(I) acetate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27752,T3D0349,Mercury(I) acetate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27753,T3D0349,Mercury(I) acetate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27754,T3D0349,Mercury(I) acetate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27755,T3D0350,Mercury(II) iodide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27756,T3D0350,Mercury(II) iodide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27757,T3D0350,Mercury(II) iodide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27758,T3D0350,Mercury(II) iodide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27759,T3D0350,Mercury(II) iodide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27760,T3D0350,Mercury(II) iodide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27761,T3D0350,Mercury(II) iodide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27762,T3D0350,Mercury(II) iodide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27763,T3D0350,Mercury(II) iodide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27764,T3D0350,Mercury(II) iodide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27765,T3D0350,Mercury(II) iodide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27766,T3D0350,Mercury(II) iodide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27767,T3D0350,Mercury(II) iodide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27768,T3D0350,Mercury(II) iodide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27769,T3D0350,Mercury(II) iodide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27770,T3D0350,Mercury(II) iodide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27771,T3D0350,Mercury(II) iodide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27772,T3D0350,Mercury(II) iodide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27773,T3D0350,Mercury(II) iodide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27774,T3D0350,Mercury(II) iodide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27775,T3D0350,Mercury(II) iodide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27776,T3D0350,Mercury(II) iodide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27777,T3D0350,Mercury(II) iodide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27778,T3D0350,Mercury(II) iodide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27779,T3D0350,Mercury(II) iodide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27780,T3D0350,Mercury(II) iodide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27781,T3D0350,Mercury(II) iodide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27782,T3D0350,Mercury(II) iodide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27783,T3D0350,Mercury(II) iodide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27784,T3D0350,Mercury(II) iodide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27785,T3D0351,Mercury(I) iodide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27786,T3D0351,Mercury(I) iodide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27787,T3D0351,Mercury(I) iodide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27788,T3D0351,Mercury(I) iodide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27789,T3D0351,Mercury(I) iodide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27790,T3D0351,Mercury(I) iodide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27791,T3D0351,Mercury(I) iodide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27792,T3D0351,Mercury(I) iodide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27793,T3D0351,Mercury(I) iodide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27794,T3D0351,Mercury(I) iodide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27795,T3D0351,Mercury(I) iodide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27796,T3D0351,Mercury(I) iodide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27797,T3D0351,Mercury(I) iodide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27798,T3D0351,Mercury(I) iodide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27799,T3D0351,Mercury(I) iodide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27800,T3D0351,Mercury(I) iodide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27801,T3D0351,Mercury(I) iodide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27802,T3D0351,Mercury(I) iodide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27803,T3D0351,Mercury(I) iodide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27804,T3D0351,Mercury(I) iodide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27805,T3D0351,Mercury(I) iodide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27806,T3D0351,Mercury(I) iodide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27807,T3D0351,Mercury(I) iodide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27808,T3D0351,Mercury(I) iodide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27809,T3D0351,Mercury(I) iodide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27810,T3D0351,Mercury(I) iodide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27811,T3D0351,Mercury(I) iodide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27812,T3D0351,Mercury(I) iodide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27813,T3D0351,Mercury(I) iodide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27814,T3D0352,Mercury(I) bromide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27815,T3D0352,Mercury(I) bromide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27816,T3D0352,Mercury(I) bromide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27817,T3D0352,Mercury(I) bromide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27818,T3D0352,Mercury(I) bromide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27819,T3D0352,Mercury(I) bromide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27820,T3D0352,Mercury(I) bromide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27821,T3D0352,Mercury(I) bromide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27822,T3D0352,Mercury(I) bromide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27823,T3D0352,Mercury(I) bromide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27824,T3D0352,Mercury(I) bromide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27825,T3D0352,Mercury(I) bromide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27826,T3D0352,Mercury(I) bromide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27827,T3D0352,Mercury(I) bromide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27828,T3D0352,Mercury(I) bromide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27829,T3D0352,Mercury(I) bromide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27830,T3D0352,Mercury(I) bromide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27831,T3D0352,Mercury(I) bromide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27832,T3D0352,Mercury(I) bromide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27833,T3D0352,Mercury(I) bromide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27834,T3D0352,Mercury(I) bromide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27835,T3D0352,Mercury(I) bromide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27836,T3D0352,Mercury(I) bromide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27837,T3D0352,Mercury(I) bromide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27838,T3D0352,Mercury(I) bromide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27839,T3D0352,Mercury(I) bromide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27840,T3D0352,Mercury(I) bromide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27841,T3D0352,Mercury(I) bromide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27842,T3D0352,Mercury(I) bromide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27843,T3D0352,Mercury(I) bromide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27844,T3D0353,Mercury(II) bromide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27845,T3D0353,Mercury(II) bromide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27846,T3D0353,Mercury(II) bromide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27847,T3D0353,Mercury(II) bromide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27848,T3D0353,Mercury(II) bromide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27849,T3D0353,Mercury(II) bromide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27850,T3D0353,Mercury(II) bromide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27851,T3D0353,Mercury(II) bromide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27852,T3D0353,Mercury(II) bromide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27853,T3D0353,Mercury(II) bromide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27854,T3D0353,Mercury(II) bromide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27855,T3D0353,Mercury(II) bromide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27856,T3D0353,Mercury(II) bromide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27857,T3D0353,Mercury(II) bromide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27858,T3D0353,Mercury(II) bromide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27859,T3D0353,Mercury(II) bromide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27860,T3D0353,Mercury(II) bromide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27861,T3D0353,Mercury(II) bromide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27862,T3D0353,Mercury(II) bromide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27863,T3D0353,Mercury(II) bromide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27864,T3D0353,Mercury(II) bromide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27865,T3D0353,Mercury(II) bromide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27866,T3D0353,Mercury(II) bromide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27867,T3D0353,Mercury(II) bromide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27868,T3D0353,Mercury(II) bromide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27869,T3D0353,Mercury(II) bromide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27870,T3D0353,Mercury(II) bromide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27871,T3D0353,Mercury(II) bromide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27872,T3D0353,Mercury(II) bromide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27873,T3D0353,Mercury(II) bromide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27874,T3D0354,Mercury(II) nitrate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27875,T3D0354,Mercury(II) nitrate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27876,T3D0354,Mercury(II) nitrate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27877,T3D0354,Mercury(II) nitrate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27878,T3D0354,Mercury(II) nitrate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27879,T3D0354,Mercury(II) nitrate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27880,T3D0354,Mercury(II) nitrate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27881,T3D0354,Mercury(II) nitrate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27882,T3D0354,Mercury(II) nitrate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27883,T3D0354,Mercury(II) nitrate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27884,T3D0354,Mercury(II) nitrate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27885,T3D0354,Mercury(II) nitrate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27886,T3D0354,Mercury(II) nitrate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27887,T3D0354,Mercury(II) nitrate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27888,T3D0354,Mercury(II) nitrate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27889,T3D0354,Mercury(II) nitrate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27890,T3D0354,Mercury(II) nitrate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27891,T3D0354,Mercury(II) nitrate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27892,T3D0354,Mercury(II) nitrate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27893,T3D0354,Mercury(II) nitrate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27894,T3D0354,Mercury(II) nitrate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27895,T3D0354,Mercury(II) nitrate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27896,T3D0354,Mercury(II) nitrate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27897,T3D0354,Mercury(II) nitrate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27898,T3D0354,Mercury(II) nitrate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27899,T3D0354,Mercury(II) nitrate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27900,T3D0354,Mercury(II) nitrate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27901,T3D0354,Mercury(II) nitrate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27902,T3D0354,Mercury(II) nitrate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27903,T3D0354,Mercury(II) nitrate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27904,T3D0355,Mercury(I) nitrate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27905,T3D0355,Mercury(I) nitrate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27906,T3D0355,Mercury(I) nitrate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27907,T3D0355,Mercury(I) nitrate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27908,T3D0355,Mercury(I) nitrate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27909,T3D0355,Mercury(I) nitrate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27910,T3D0355,Mercury(I) nitrate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27911,T3D0355,Mercury(I) nitrate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27912,T3D0355,Mercury(I) nitrate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27913,T3D0355,Mercury(I) nitrate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27914,T3D0355,Mercury(I) nitrate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27915,T3D0355,Mercury(I) nitrate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27916,T3D0355,Mercury(I) nitrate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27917,T3D0355,Mercury(I) nitrate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27918,T3D0355,Mercury(I) nitrate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27919,T3D0355,Mercury(I) nitrate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27920,T3D0355,Mercury(I) nitrate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27921,T3D0355,Mercury(I) nitrate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27922,T3D0355,Mercury(I) nitrate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27923,T3D0355,Mercury(I) nitrate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27924,T3D0355,Mercury(I) nitrate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27925,T3D0355,Mercury(I) nitrate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27926,T3D0355,Mercury(I) nitrate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27927,T3D0355,Mercury(I) nitrate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27928,T3D0355,Mercury(I) nitrate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27929,T3D0355,Mercury(I) nitrate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27930,T3D0355,Mercury(I) nitrate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27931,T3D0355,Mercury(I) nitrate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27932,T3D0355,Mercury(I) nitrate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27933,T3D0355,Mercury(I) nitrate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27934,T3D0356,Mercury(II) thiocyanate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27935,T3D0356,Mercury(II) thiocyanate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27936,T3D0356,Mercury(II) thiocyanate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27937,T3D0356,Mercury(II) thiocyanate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27938,T3D0356,Mercury(II) thiocyanate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27939,T3D0356,Mercury(II) thiocyanate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27940,T3D0356,Mercury(II) thiocyanate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27941,T3D0356,Mercury(II) thiocyanate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27942,T3D0356,Mercury(II) thiocyanate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27943,T3D0356,Mercury(II) thiocyanate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27944,T3D0356,Mercury(II) thiocyanate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27945,T3D0356,Mercury(II) thiocyanate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27946,T3D0356,Mercury(II) thiocyanate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27947,T3D0356,Mercury(II) thiocyanate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27948,T3D0356,Mercury(II) thiocyanate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27949,T3D0356,Mercury(II) thiocyanate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27950,T3D0356,Mercury(II) thiocyanate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27951,T3D0356,Mercury(II) thiocyanate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27952,T3D0356,Mercury(II) thiocyanate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27953,T3D0356,Mercury(II) thiocyanate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27954,T3D0356,Mercury(II) thiocyanate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27955,T3D0356,Mercury(II) thiocyanate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27956,T3D0356,Mercury(II) thiocyanate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27957,T3D0356,Mercury(II) thiocyanate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27958,T3D0356,Mercury(II) thiocyanate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27959,T3D0356,Mercury(II) thiocyanate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27960,T3D0356,Mercury(II) thiocyanate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27961,T3D0356,Mercury(II) thiocyanate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27962,T3D0356,Mercury(II) thiocyanate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27963,T3D0356,Mercury(II) thiocyanate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27964,T3D0357,Mercury(II) sulfate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27965,T3D0357,Mercury(II) sulfate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27966,T3D0357,Mercury(II) sulfate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27967,T3D0357,Mercury(II) sulfate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27968,T3D0357,Mercury(II) sulfate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27969,T3D0357,Mercury(II) sulfate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27970,T3D0357,Mercury(II) sulfate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27971,T3D0357,Mercury(II) sulfate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27972,T3D0357,Mercury(II) sulfate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27973,T3D0357,Mercury(II) sulfate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27974,T3D0357,Mercury(II) sulfate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27975,T3D0357,Mercury(II) sulfate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27976,T3D0357,Mercury(II) sulfate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27977,T3D0357,Mercury(II) sulfate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27978,T3D0357,Mercury(II) sulfate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27979,T3D0357,Mercury(II) sulfate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27980,T3D0357,Mercury(II) sulfate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27981,T3D0357,Mercury(II) sulfate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27982,T3D0357,Mercury(II) sulfate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27983,T3D0357,Mercury(II) sulfate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27984,T3D0357,Mercury(II) sulfate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27985,T3D0357,Mercury(II) sulfate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27986,T3D0357,Mercury(II) sulfate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27987,T3D0357,Mercury(II) sulfate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27988,T3D0357,Mercury(II) sulfate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27989,T3D0357,Mercury(II) sulfate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27990,T3D0357,Mercury(II) sulfate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27991,T3D0357,Mercury(II) sulfate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27992,T3D0357,Mercury(II) sulfate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27993,T3D0357,Mercury(II) sulfate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
27994,T3D0358,Mercury(I) sulfate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27995,T3D0358,Mercury(I) sulfate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27996,T3D0358,Mercury(I) sulfate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27997,T3D0358,Mercury(I) sulfate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27998,T3D0358,Mercury(I) sulfate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
27999,T3D0358,Mercury(I) sulfate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28000,T3D0358,Mercury(I) sulfate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28001,T3D0358,Mercury(I) sulfate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28002,T3D0358,Mercury(I) sulfate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28003,T3D0358,Mercury(I) sulfate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28004,T3D0358,Mercury(I) sulfate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28005,T3D0358,Mercury(I) sulfate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28006,T3D0358,Mercury(I) sulfate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28007,T3D0358,Mercury(I) sulfate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28008,T3D0358,Mercury(I) sulfate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28009,T3D0358,Mercury(I) sulfate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28010,T3D0358,Mercury(I) sulfate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28011,T3D0358,Mercury(I) sulfate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28012,T3D0358,Mercury(I) sulfate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28013,T3D0358,Mercury(I) sulfate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28014,T3D0358,Mercury(I) sulfate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28015,T3D0358,Mercury(I) sulfate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28016,T3D0358,Mercury(I) sulfate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28017,T3D0358,Mercury(I) sulfate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28018,T3D0358,Mercury(I) sulfate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28019,T3D0358,Mercury(I) sulfate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28020,T3D0358,Mercury(I) sulfate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28021,T3D0358,Mercury(I) sulfate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28022,T3D0358,Mercury(I) sulfate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28023,T3D0358,Mercury(I) sulfate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28024,T3D0360,Methylmercuric chloride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28025,T3D0360,Methylmercuric chloride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28026,T3D0360,Methylmercuric chloride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28027,T3D0360,Methylmercuric chloride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28028,T3D0360,Methylmercuric chloride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28029,T3D0360,Methylmercuric chloride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28030,T3D0360,Methylmercuric chloride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28031,T3D0360,Methylmercuric chloride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28032,T3D0360,Methylmercuric chloride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28033,T3D0360,Methylmercuric chloride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28034,T3D0360,Methylmercuric chloride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28035,T3D0360,Methylmercuric chloride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28036,T3D0360,Methylmercuric chloride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28037,T3D0360,Methylmercuric chloride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28038,T3D0360,Methylmercuric chloride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28039,T3D0360,Methylmercuric chloride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28040,T3D0360,Methylmercuric chloride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28041,T3D0360,Methylmercuric chloride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28042,T3D0360,Methylmercuric chloride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28043,T3D0360,Methylmercuric chloride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28044,T3D0360,Methylmercuric chloride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28045,T3D0360,Methylmercuric chloride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28046,T3D0360,Methylmercuric chloride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28047,T3D0360,Methylmercuric chloride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28048,T3D0360,Methylmercuric chloride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28049,T3D0360,Methylmercuric chloride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28050,T3D0360,Methylmercuric chloride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28051,T3D0360,Methylmercuric chloride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28052,T3D0360,Methylmercuric chloride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28053,T3D0360,Methylmercuric chloride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28054,T3D0362,Mercuric potassium iodide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28055,T3D0362,Mercuric potassium iodide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28056,T3D0362,Mercuric potassium iodide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28057,T3D0362,Mercuric potassium iodide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28058,T3D0362,Mercuric potassium iodide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28059,T3D0362,Mercuric potassium iodide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28060,T3D0362,Mercuric potassium iodide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28061,T3D0362,Mercuric potassium iodide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28062,T3D0362,Mercuric potassium iodide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28063,T3D0362,Mercuric potassium iodide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28064,T3D0362,Mercuric potassium iodide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28065,T3D0362,Mercuric potassium iodide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28066,T3D0362,Mercuric potassium iodide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28067,T3D0362,Mercuric potassium iodide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28068,T3D0362,Mercuric potassium iodide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28069,T3D0362,Mercuric potassium iodide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28070,T3D0362,Mercuric potassium iodide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28071,T3D0362,Mercuric potassium iodide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28072,T3D0362,Mercuric potassium iodide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28073,T3D0362,Mercuric potassium iodide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28074,T3D0362,Mercuric potassium iodide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28075,T3D0362,Mercuric potassium iodide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28076,T3D0362,Mercuric potassium iodide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28077,T3D0362,Mercuric potassium iodide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28078,T3D0362,Mercuric potassium iodide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28079,T3D0362,Mercuric potassium iodide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28080,T3D0362,Mercuric potassium iodide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28081,T3D0362,Mercuric potassium iodide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28082,T3D0362,Mercuric potassium iodide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28083,T3D0362,Mercuric potassium iodide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28084,T3D0362,Mercuric potassium iodide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28085,T3D0362,Mercuric potassium iodide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28086,T3D0362,Mercuric potassium iodide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28087,T3D0362,Mercuric potassium iodide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28088,T3D0362,Mercuric potassium iodide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28089,T3D0362,Mercuric potassium iodide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28090,T3D0362,Mercuric potassium iodide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28091,T3D0362,Mercuric potassium iodide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28092,T3D0362,Mercuric potassium iodide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28093,T3D0362,Mercuric potassium iodide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28094,T3D0362,Mercuric potassium iodide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28095,T3D0362,Mercuric potassium iodide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28096,T3D0362,Mercuric potassium iodide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28097,T3D0362,Mercuric potassium iodide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28098,T3D0362,Mercuric potassium iodide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28099,T3D0362,Mercuric potassium iodide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28100,T3D0362,Mercuric potassium iodide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28101,T3D0362,Mercuric potassium iodide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28102,T3D0362,Mercuric potassium iodide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28103,T3D0363,Mercury(II) cyanide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28104,T3D0363,Mercury(II) cyanide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28105,T3D0363,Mercury(II) cyanide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28106,T3D0363,Mercury(II) cyanide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28107,T3D0363,Mercury(II) cyanide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28108,T3D0363,Mercury(II) cyanide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28109,T3D0363,Mercury(II) cyanide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28110,T3D0363,Mercury(II) cyanide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28111,T3D0363,Mercury(II) cyanide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28112,T3D0363,Mercury(II) cyanide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28113,T3D0363,Mercury(II) cyanide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28114,T3D0363,Mercury(II) cyanide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28115,T3D0363,Mercury(II) cyanide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28116,T3D0363,Mercury(II) cyanide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28117,T3D0363,Mercury(II) cyanide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28118,T3D0363,Mercury(II) cyanide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28119,T3D0363,Mercury(II) cyanide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28120,T3D0363,Mercury(II) cyanide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28121,T3D0363,Mercury(II) cyanide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28122,T3D0363,Mercury(II) cyanide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28123,T3D0363,Mercury(II) cyanide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28124,T3D0363,Mercury(II) cyanide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28125,T3D0363,Mercury(II) cyanide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28126,T3D0363,Mercury(II) cyanide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28127,T3D0363,Mercury(II) cyanide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28128,T3D0363,Mercury(II) cyanide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28129,T3D0363,Mercury(II) cyanide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28130,T3D0363,Mercury(II) cyanide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28131,T3D0363,Mercury(II) cyanide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28132,T3D0363,Mercury(II) cyanide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28133,T3D1341,Mercuric amidochloride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28134,T3D1341,Mercuric amidochloride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28135,T3D1341,Mercuric amidochloride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28136,T3D1341,Mercuric amidochloride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28137,T3D1341,Mercuric amidochloride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28138,T3D1341,Mercuric amidochloride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28139,T3D1341,Mercuric amidochloride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28140,T3D1341,Mercuric amidochloride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28141,T3D1341,Mercuric amidochloride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28142,T3D1341,Mercuric amidochloride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28143,T3D1341,Mercuric amidochloride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28144,T3D1341,Mercuric amidochloride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28145,T3D1341,Mercuric amidochloride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28146,T3D1341,Mercuric amidochloride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28147,T3D1341,Mercuric amidochloride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28148,T3D1341,Mercuric amidochloride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28149,T3D1341,Mercuric amidochloride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28150,T3D1341,Mercuric amidochloride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28151,T3D1341,Mercuric amidochloride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28152,T3D1341,Mercuric amidochloride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28153,T3D1341,Mercuric amidochloride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28154,T3D1341,Mercuric amidochloride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28155,T3D1341,Mercuric amidochloride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28156,T3D1341,Mercuric amidochloride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28157,T3D1341,Mercuric amidochloride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28158,T3D1341,Mercuric amidochloride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28159,T3D1341,Mercuric amidochloride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28160,T3D1341,Mercuric amidochloride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28161,T3D1341,Mercuric amidochloride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28162,T3D1341,Mercuric amidochloride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28163,T3D1341,Mercuric amidochloride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28164,T3D1341,Mercuric amidochloride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28165,T3D1341,Mercuric amidochloride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28166,T3D1341,Mercuric amidochloride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28167,T3D1341,Mercuric amidochloride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28168,T3D1341,Mercuric amidochloride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28169,T3D1341,Mercuric amidochloride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28170,T3D1341,Mercuric amidochloride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28171,T3D1341,Mercuric amidochloride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28172,T3D1341,Mercuric amidochloride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28173,T3D1341,Mercuric amidochloride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28174,T3D1341,Mercuric amidochloride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28175,T3D1341,Mercuric amidochloride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28176,T3D1341,Mercuric amidochloride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28177,T3D1341,Mercuric amidochloride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28178,T3D1341,Mercuric amidochloride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28179,T3D1341,Mercuric amidochloride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28180,T3D1341,Mercuric amidochloride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28181,T3D1341,Mercuric amidochloride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28182,T3D1341,Mercuric amidochloride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28183,T3D1342,Mercury(I) fluoride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28184,T3D1342,Mercury(I) fluoride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28185,T3D1342,Mercury(I) fluoride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28186,T3D1342,Mercury(I) fluoride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28187,T3D1342,Mercury(I) fluoride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28188,T3D1342,Mercury(I) fluoride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28189,T3D1342,Mercury(I) fluoride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28190,T3D1342,Mercury(I) fluoride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28191,T3D1342,Mercury(I) fluoride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28192,T3D1342,Mercury(I) fluoride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28193,T3D1342,Mercury(I) fluoride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28194,T3D1342,Mercury(I) fluoride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28195,T3D1342,Mercury(I) fluoride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28196,T3D1342,Mercury(I) fluoride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28197,T3D1342,Mercury(I) fluoride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28198,T3D1342,Mercury(I) fluoride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28199,T3D1342,Mercury(I) fluoride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28200,T3D1342,Mercury(I) fluoride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28201,T3D1342,Mercury(I) fluoride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28202,T3D1342,Mercury(I) fluoride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28203,T3D1342,Mercury(I) fluoride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28204,T3D1342,Mercury(I) fluoride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28205,T3D1342,Mercury(I) fluoride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28206,T3D1342,Mercury(I) fluoride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28207,T3D1342,Mercury(I) fluoride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28208,T3D1342,Mercury(I) fluoride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28209,T3D1342,Mercury(I) fluoride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28210,T3D1342,Mercury(I) fluoride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28211,T3D1342,Mercury(I) fluoride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28212,T3D1342,Mercury(I) fluoride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28213,T3D1342,Mercury(I) fluoride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28214,T3D1342,Mercury(I) fluoride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28215,T3D1342,Mercury(I) fluoride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28216,T3D1342,Mercury(I) fluoride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28217,T3D1342,Mercury(I) fluoride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28218,T3D1342,Mercury(I) fluoride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28219,T3D1342,Mercury(I) fluoride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28220,T3D1342,Mercury(I) fluoride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28221,T3D1342,Mercury(I) fluoride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28222,T3D1342,Mercury(I) fluoride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28223,T3D1342,Mercury(I) fluoride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28224,T3D1342,Mercury(I) fluoride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28225,T3D1342,Mercury(I) fluoride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28226,T3D1342,Mercury(I) fluoride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28227,T3D1342,Mercury(I) fluoride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28228,T3D1342,Mercury(I) fluoride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28229,T3D1342,Mercury(I) fluoride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28230,T3D1342,Mercury(I) fluoride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28231,T3D1342,Mercury(I) fluoride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28232,T3D1342,Mercury(I) fluoride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28233,T3D1343,Mercury(II) fluoride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28234,T3D1343,Mercury(II) fluoride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28235,T3D1343,Mercury(II) fluoride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28236,T3D1343,Mercury(II) fluoride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28237,T3D1343,Mercury(II) fluoride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28238,T3D1343,Mercury(II) fluoride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28239,T3D1343,Mercury(II) fluoride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28240,T3D1343,Mercury(II) fluoride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28241,T3D1343,Mercury(II) fluoride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28242,T3D1343,Mercury(II) fluoride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28243,T3D1343,Mercury(II) fluoride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28244,T3D1343,Mercury(II) fluoride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28245,T3D1343,Mercury(II) fluoride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28246,T3D1343,Mercury(II) fluoride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28247,T3D1343,Mercury(II) fluoride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28248,T3D1343,Mercury(II) fluoride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28249,T3D1343,Mercury(II) fluoride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28250,T3D1343,Mercury(II) fluoride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28251,T3D1343,Mercury(II) fluoride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28252,T3D1343,Mercury(II) fluoride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28253,T3D1343,Mercury(II) fluoride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28254,T3D1343,Mercury(II) fluoride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28255,T3D1343,Mercury(II) fluoride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28256,T3D1343,Mercury(II) fluoride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28257,T3D1343,Mercury(II) fluoride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28258,T3D1343,Mercury(II) fluoride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28259,T3D1343,Mercury(II) fluoride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28260,T3D1343,Mercury(II) fluoride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28261,T3D1343,Mercury(II) fluoride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28262,T3D1343,Mercury(II) fluoride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28263,T3D1343,Mercury(II) fluoride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28264,T3D1343,Mercury(II) fluoride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28265,T3D1343,Mercury(II) fluoride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28266,T3D1343,Mercury(II) fluoride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28267,T3D1343,Mercury(II) fluoride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28268,T3D1343,Mercury(II) fluoride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28269,T3D1343,Mercury(II) fluoride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28270,T3D1343,Mercury(II) fluoride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28271,T3D1343,Mercury(II) fluoride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28272,T3D1343,Mercury(II) fluoride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28273,T3D1343,Mercury(II) fluoride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28274,T3D1343,Mercury(II) fluoride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28275,T3D1343,Mercury(II) fluoride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28276,T3D1343,Mercury(II) fluoride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28277,T3D1343,Mercury(II) fluoride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28278,T3D1343,Mercury(II) fluoride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28279,T3D1343,Mercury(II) fluoride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28280,T3D1343,Mercury(II) fluoride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28281,T3D1343,Mercury(II) fluoride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28282,T3D1343,Mercury(II) fluoride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28283,T3D1344,Mercury(I) oxide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28284,T3D1344,Mercury(I) oxide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28285,T3D1344,Mercury(I) oxide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28286,T3D1344,Mercury(I) oxide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28287,T3D1344,Mercury(I) oxide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28288,T3D1344,Mercury(I) oxide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28289,T3D1344,Mercury(I) oxide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28290,T3D1344,Mercury(I) oxide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28291,T3D1344,Mercury(I) oxide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28292,T3D1344,Mercury(I) oxide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28293,T3D1344,Mercury(I) oxide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28294,T3D1344,Mercury(I) oxide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28295,T3D1344,Mercury(I) oxide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28296,T3D1344,Mercury(I) oxide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28297,T3D1344,Mercury(I) oxide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28298,T3D1344,Mercury(I) oxide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28299,T3D1344,Mercury(I) oxide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28300,T3D1344,Mercury(I) oxide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28301,T3D1344,Mercury(I) oxide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28302,T3D1344,Mercury(I) oxide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28303,T3D1344,Mercury(I) oxide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28304,T3D1344,Mercury(I) oxide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28305,T3D1344,Mercury(I) oxide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28306,T3D1344,Mercury(I) oxide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28307,T3D1344,Mercury(I) oxide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28308,T3D1344,Mercury(I) oxide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28309,T3D1344,Mercury(I) oxide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28310,T3D1344,Mercury(I) oxide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28311,T3D1344,Mercury(I) oxide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28312,T3D1344,Mercury(I) oxide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28313,T3D1344,Mercury(I) oxide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28314,T3D1344,Mercury(I) oxide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28315,T3D1344,Mercury(I) oxide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28316,T3D1344,Mercury(I) oxide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28317,T3D1344,Mercury(I) oxide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28318,T3D1344,Mercury(I) oxide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28319,T3D1344,Mercury(I) oxide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28320,T3D1344,Mercury(I) oxide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28321,T3D1344,Mercury(I) oxide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28322,T3D1344,Mercury(I) oxide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28323,T3D1344,Mercury(I) oxide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28324,T3D1344,Mercury(I) oxide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28325,T3D1344,Mercury(I) oxide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28326,T3D1344,Mercury(I) oxide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28327,T3D1344,Mercury(I) oxide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28328,T3D1344,Mercury(I) oxide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28329,T3D1344,Mercury(I) oxide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28330,T3D1344,Mercury(I) oxide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28331,T3D1344,Mercury(I) oxide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28332,T3D1344,Mercury(I) oxide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28333,T3D1345,Mercury oxide sulfate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28334,T3D1345,Mercury oxide sulfate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28335,T3D1345,Mercury oxide sulfate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28336,T3D1345,Mercury oxide sulfate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28337,T3D1345,Mercury oxide sulfate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28338,T3D1345,Mercury oxide sulfate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28339,T3D1345,Mercury oxide sulfate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28340,T3D1345,Mercury oxide sulfate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28341,T3D1345,Mercury oxide sulfate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28342,T3D1345,Mercury oxide sulfate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28343,T3D1345,Mercury oxide sulfate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28344,T3D1345,Mercury oxide sulfate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28345,T3D1345,Mercury oxide sulfate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28346,T3D1345,Mercury oxide sulfate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28347,T3D1345,Mercury oxide sulfate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28348,T3D1345,Mercury oxide sulfate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28349,T3D1345,Mercury oxide sulfate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28350,T3D1345,Mercury oxide sulfate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28351,T3D1345,Mercury oxide sulfate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28352,T3D1345,Mercury oxide sulfate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28353,T3D1345,Mercury oxide sulfate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28354,T3D1345,Mercury oxide sulfate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28355,T3D1345,Mercury oxide sulfate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28356,T3D1345,Mercury oxide sulfate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28357,T3D1345,Mercury oxide sulfate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28358,T3D1345,Mercury oxide sulfate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28359,T3D1345,Mercury oxide sulfate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28360,T3D1345,Mercury oxide sulfate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28361,T3D1345,Mercury oxide sulfate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28362,T3D1345,Mercury oxide sulfate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28363,T3D1345,Mercury oxide sulfate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28364,T3D1345,Mercury oxide sulfate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28365,T3D1345,Mercury oxide sulfate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28366,T3D1345,Mercury oxide sulfate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28367,T3D1345,Mercury oxide sulfate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28368,T3D1345,Mercury oxide sulfate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28369,T3D1345,Mercury oxide sulfate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28370,T3D1345,Mercury oxide sulfate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28371,T3D1345,Mercury oxide sulfate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28372,T3D1345,Mercury oxide sulfate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28373,T3D1345,Mercury oxide sulfate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28374,T3D1345,Mercury oxide sulfate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28375,T3D1345,Mercury oxide sulfate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28376,T3D1345,Mercury oxide sulfate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28377,T3D1345,Mercury oxide sulfate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28378,T3D1345,Mercury oxide sulfate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28379,T3D1345,Mercury oxide sulfate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28380,T3D1345,Mercury oxide sulfate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28381,T3D1345,Mercury oxide sulfate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28382,T3D1345,Mercury oxide sulfate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28383,T3D1346,Cadmium mercury sulfide,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28384,T3D1346,Cadmium mercury sulfide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28385,T3D1346,Cadmium mercury sulfide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28386,T3D1346,Cadmium mercury sulfide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28387,T3D1346,Cadmium mercury sulfide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28388,T3D1346,Cadmium mercury sulfide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28389,T3D1346,Cadmium mercury sulfide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28390,T3D1346,Cadmium mercury sulfide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28391,T3D1346,Cadmium mercury sulfide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28392,T3D1346,Cadmium mercury sulfide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28393,T3D1346,Cadmium mercury sulfide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28394,T3D1346,Cadmium mercury sulfide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28395,T3D1346,Cadmium mercury sulfide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28396,T3D1346,Cadmium mercury sulfide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28397,T3D1346,Cadmium mercury sulfide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28398,T3D1346,Cadmium mercury sulfide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28399,T3D1346,Cadmium mercury sulfide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28400,T3D1346,Cadmium mercury sulfide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28401,T3D1346,Cadmium mercury sulfide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28402,T3D1346,Cadmium mercury sulfide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28403,T3D1346,Cadmium mercury sulfide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28404,T3D1346,Cadmium mercury sulfide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28405,T3D1346,Cadmium mercury sulfide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28406,T3D1346,Cadmium mercury sulfide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28407,T3D1346,Cadmium mercury sulfide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28408,T3D1346,Cadmium mercury sulfide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28409,T3D1346,Cadmium mercury sulfide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28410,T3D1346,Cadmium mercury sulfide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28411,T3D1346,Cadmium mercury sulfide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28412,T3D1346,Cadmium mercury sulfide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28413,T3D1346,Cadmium mercury sulfide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28414,T3D1346,Cadmium mercury sulfide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28415,T3D1346,Cadmium mercury sulfide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28416,T3D1346,Cadmium mercury sulfide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28417,T3D1346,Cadmium mercury sulfide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28418,T3D1346,Cadmium mercury sulfide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28419,T3D1346,Cadmium mercury sulfide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28420,T3D1346,Cadmium mercury sulfide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28421,T3D1346,Cadmium mercury sulfide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28422,T3D1346,Cadmium mercury sulfide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28423,T3D1346,Cadmium mercury sulfide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28424,T3D1346,Cadmium mercury sulfide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28425,T3D1346,Cadmium mercury sulfide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28426,T3D1346,Cadmium mercury sulfide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28427,T3D1346,Cadmium mercury sulfide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28428,T3D1346,Cadmium mercury sulfide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28429,T3D1346,Cadmium mercury sulfide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28430,T3D1346,Cadmium mercury sulfide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28431,T3D1346,Cadmium mercury sulfide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28432,T3D1346,Cadmium mercury sulfide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28433,T3D1347,Mercuric potassium cyanide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28434,T3D1347,Mercuric potassium cyanide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28435,T3D1347,Mercuric potassium cyanide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28436,T3D1347,Mercuric potassium cyanide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28437,T3D1347,Mercuric potassium cyanide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28438,T3D1347,Mercuric potassium cyanide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28439,T3D1347,Mercuric potassium cyanide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28440,T3D1347,Mercuric potassium cyanide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28441,T3D1347,Mercuric potassium cyanide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28442,T3D1347,Mercuric potassium cyanide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28443,T3D1347,Mercuric potassium cyanide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28444,T3D1347,Mercuric potassium cyanide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28445,T3D1347,Mercuric potassium cyanide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28446,T3D1347,Mercuric potassium cyanide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28447,T3D1347,Mercuric potassium cyanide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28448,T3D1347,Mercuric potassium cyanide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28449,T3D1347,Mercuric potassium cyanide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28450,T3D1347,Mercuric potassium cyanide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28451,T3D1347,Mercuric potassium cyanide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28452,T3D1347,Mercuric potassium cyanide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28453,T3D1347,Mercuric potassium cyanide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28454,T3D1347,Mercuric potassium cyanide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28455,T3D1347,Mercuric potassium cyanide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28456,T3D1347,Mercuric potassium cyanide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28457,T3D1347,Mercuric potassium cyanide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28458,T3D1347,Mercuric potassium cyanide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28459,T3D1347,Mercuric potassium cyanide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28460,T3D1347,Mercuric potassium cyanide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28461,T3D1347,Mercuric potassium cyanide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28462,T3D1347,Mercuric potassium cyanide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28463,T3D1347,Mercuric potassium cyanide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28464,T3D1347,Mercuric potassium cyanide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28465,T3D1347,Mercuric potassium cyanide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28466,T3D1347,Mercuric potassium cyanide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28467,T3D1347,Mercuric potassium cyanide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28468,T3D1347,Mercuric potassium cyanide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28469,T3D1347,Mercuric potassium cyanide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28470,T3D1347,Mercuric potassium cyanide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28471,T3D1347,Mercuric potassium cyanide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28472,T3D1347,Mercuric potassium cyanide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28473,T3D1347,Mercuric potassium cyanide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28474,T3D1347,Mercuric potassium cyanide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28475,T3D1347,Mercuric potassium cyanide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28476,T3D1347,Mercuric potassium cyanide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28477,T3D1347,Mercuric potassium cyanide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28478,T3D1347,Mercuric potassium cyanide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28479,T3D1347,Mercuric potassium cyanide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28480,T3D1347,Mercuric potassium cyanide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28481,T3D1347,Mercuric potassium cyanide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28482,T3D1348,Mercuric benzoate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28483,T3D1348,Mercuric benzoate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28484,T3D1348,Mercuric benzoate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28485,T3D1348,Mercuric benzoate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28486,T3D1348,Mercuric benzoate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28487,T3D1348,Mercuric benzoate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28488,T3D1348,Mercuric benzoate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28489,T3D1348,Mercuric benzoate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28490,T3D1348,Mercuric benzoate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28491,T3D1348,Mercuric benzoate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28492,T3D1348,Mercuric benzoate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28493,T3D1348,Mercuric benzoate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28494,T3D1348,Mercuric benzoate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28495,T3D1348,Mercuric benzoate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28496,T3D1348,Mercuric benzoate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28497,T3D1348,Mercuric benzoate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28498,T3D1348,Mercuric benzoate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28499,T3D1348,Mercuric benzoate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28500,T3D1348,Mercuric benzoate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28501,T3D1348,Mercuric benzoate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28502,T3D1348,Mercuric benzoate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28503,T3D1348,Mercuric benzoate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28504,T3D1348,Mercuric benzoate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28505,T3D1348,Mercuric benzoate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28506,T3D1348,Mercuric benzoate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28507,T3D1348,Mercuric benzoate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28508,T3D1348,Mercuric benzoate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28509,T3D1348,Mercuric benzoate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28510,T3D1348,Mercuric benzoate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28511,T3D1348,Mercuric benzoate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28512,T3D1348,Mercuric benzoate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28513,T3D1348,Mercuric benzoate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28514,T3D1348,Mercuric benzoate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28515,T3D1348,Mercuric benzoate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28516,T3D1348,Mercuric benzoate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28517,T3D1348,Mercuric benzoate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28518,T3D1348,Mercuric benzoate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28519,T3D1348,Mercuric benzoate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28520,T3D1348,Mercuric benzoate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28521,T3D1348,Mercuric benzoate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28522,T3D1348,Mercuric benzoate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28523,T3D1348,Mercuric benzoate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28524,T3D1348,Mercuric benzoate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28525,T3D1348,Mercuric benzoate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28526,T3D1348,Mercuric benzoate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28527,T3D1348,Mercuric benzoate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28528,T3D1348,Mercuric benzoate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28529,T3D1348,Mercuric benzoate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28530,T3D1348,Mercuric benzoate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28531,T3D1348,Mercuric benzoate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28532,T3D1349,Mercuric oleate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28533,T3D1349,Mercuric oleate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28534,T3D1349,Mercuric oleate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28535,T3D1349,Mercuric oleate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28536,T3D1349,Mercuric oleate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28537,T3D1349,Mercuric oleate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28538,T3D1349,Mercuric oleate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28539,T3D1349,Mercuric oleate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28540,T3D1349,Mercuric oleate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28541,T3D1349,Mercuric oleate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28542,T3D1349,Mercuric oleate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28543,T3D1349,Mercuric oleate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28544,T3D1349,Mercuric oleate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28545,T3D1349,Mercuric oleate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28546,T3D1349,Mercuric oleate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28547,T3D1349,Mercuric oleate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28548,T3D1349,Mercuric oleate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28549,T3D1349,Mercuric oleate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28550,T3D1349,Mercuric oleate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28551,T3D1349,Mercuric oleate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28552,T3D1349,Mercuric oleate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28553,T3D1349,Mercuric oleate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28554,T3D1349,Mercuric oleate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28555,T3D1349,Mercuric oleate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28556,T3D1349,Mercuric oleate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28557,T3D1349,Mercuric oleate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28558,T3D1349,Mercuric oleate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28559,T3D1349,Mercuric oleate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28560,T3D1349,Mercuric oleate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28561,T3D1349,Mercuric oleate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28562,T3D1349,Mercuric oleate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28563,T3D1349,Mercuric oleate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28564,T3D1349,Mercuric oleate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28565,T3D1349,Mercuric oleate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28566,T3D1349,Mercuric oleate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28567,T3D1349,Mercuric oleate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28568,T3D1349,Mercuric oleate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28569,T3D1349,Mercuric oleate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28570,T3D1349,Mercuric oleate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28571,T3D1349,Mercuric oleate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28572,T3D1349,Mercuric oleate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28573,T3D1349,Mercuric oleate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28574,T3D1349,Mercuric oleate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28575,T3D1349,Mercuric oleate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28576,T3D1349,Mercuric oleate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28577,T3D1349,Mercuric oleate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28578,T3D1349,Mercuric oleate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28579,T3D1349,Mercuric oleate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28580,T3D1349,Mercuric oleate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28581,T3D1349,Mercuric oleate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28582,T3D1350,Methylmercuric dicyanamide,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28583,T3D1350,Methylmercuric dicyanamide,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28584,T3D1350,Methylmercuric dicyanamide,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28585,T3D1350,Methylmercuric dicyanamide,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28586,T3D1350,Methylmercuric dicyanamide,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28587,T3D1350,Methylmercuric dicyanamide,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28588,T3D1350,Methylmercuric dicyanamide,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28589,T3D1350,Methylmercuric dicyanamide,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28590,T3D1350,Methylmercuric dicyanamide,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28591,T3D1350,Methylmercuric dicyanamide,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28592,T3D1350,Methylmercuric dicyanamide,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28593,T3D1350,Methylmercuric dicyanamide,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28594,T3D1350,Methylmercuric dicyanamide,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28595,T3D1350,Methylmercuric dicyanamide,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28596,T3D1350,Methylmercuric dicyanamide,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28597,T3D1350,Methylmercuric dicyanamide,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28598,T3D1350,Methylmercuric dicyanamide,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28599,T3D1350,Methylmercuric dicyanamide,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28600,T3D1350,Methylmercuric dicyanamide,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28601,T3D1350,Methylmercuric dicyanamide,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28602,T3D1350,Methylmercuric dicyanamide,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28603,T3D1350,Methylmercuric dicyanamide,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28604,T3D1350,Methylmercuric dicyanamide,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28605,T3D1350,Methylmercuric dicyanamide,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28606,T3D1350,Methylmercuric dicyanamide,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28607,T3D1350,Methylmercuric dicyanamide,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28608,T3D1350,Methylmercuric dicyanamide,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28609,T3D1350,Methylmercuric dicyanamide,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28610,T3D1350,Methylmercuric dicyanamide,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28611,T3D1350,Methylmercuric dicyanamide,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28612,T3D1350,Methylmercuric dicyanamide,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28613,T3D1350,Methylmercuric dicyanamide,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28614,T3D1350,Methylmercuric dicyanamide,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28615,T3D1350,Methylmercuric dicyanamide,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28616,T3D1350,Methylmercuric dicyanamide,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28617,T3D1350,Methylmercuric dicyanamide,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28618,T3D1350,Methylmercuric dicyanamide,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28619,T3D1350,Methylmercuric dicyanamide,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28620,T3D1350,Methylmercuric dicyanamide,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28621,T3D1350,Methylmercuric dicyanamide,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28622,T3D1350,Methylmercuric dicyanamide,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28623,T3D1350,Methylmercuric dicyanamide,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28624,T3D1350,Methylmercuric dicyanamide,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28625,T3D1350,Methylmercuric dicyanamide,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28626,T3D1350,Methylmercuric dicyanamide,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28627,T3D1350,Methylmercuric dicyanamide,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28628,T3D1350,Methylmercuric dicyanamide,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28629,T3D1350,Methylmercuric dicyanamide,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28630,T3D1350,Methylmercuric dicyanamide,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28631,T3D1351,Ethylmercuric phosphate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28632,T3D1351,Ethylmercuric phosphate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28633,T3D1351,Ethylmercuric phosphate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28634,T3D1351,Ethylmercuric phosphate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28635,T3D1351,Ethylmercuric phosphate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28636,T3D1351,Ethylmercuric phosphate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28637,T3D1351,Ethylmercuric phosphate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28638,T3D1351,Ethylmercuric phosphate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28639,T3D1351,Ethylmercuric phosphate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28640,T3D1351,Ethylmercuric phosphate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28641,T3D1351,Ethylmercuric phosphate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28642,T3D1351,Ethylmercuric phosphate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28643,T3D1351,Ethylmercuric phosphate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28644,T3D1351,Ethylmercuric phosphate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28645,T3D1351,Ethylmercuric phosphate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28646,T3D1351,Ethylmercuric phosphate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28647,T3D1351,Ethylmercuric phosphate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28648,T3D1351,Ethylmercuric phosphate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28649,T3D1351,Ethylmercuric phosphate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28650,T3D1351,Ethylmercuric phosphate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28651,T3D1351,Ethylmercuric phosphate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28652,T3D1351,Ethylmercuric phosphate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28653,T3D1351,Ethylmercuric phosphate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28654,T3D1351,Ethylmercuric phosphate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28655,T3D1351,Ethylmercuric phosphate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28656,T3D1351,Ethylmercuric phosphate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28657,T3D1351,Ethylmercuric phosphate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28658,T3D1351,Ethylmercuric phosphate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28659,T3D1351,Ethylmercuric phosphate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28660,T3D1351,Ethylmercuric phosphate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28661,T3D1351,Ethylmercuric phosphate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28662,T3D1351,Ethylmercuric phosphate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28663,T3D1351,Ethylmercuric phosphate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28664,T3D1351,Ethylmercuric phosphate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28665,T3D1351,Ethylmercuric phosphate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28666,T3D1351,Ethylmercuric phosphate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28667,T3D1351,Ethylmercuric phosphate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28668,T3D1351,Ethylmercuric phosphate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28669,T3D1351,Ethylmercuric phosphate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28670,T3D1351,Ethylmercuric phosphate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28671,T3D1351,Ethylmercuric phosphate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28672,T3D1351,Ethylmercuric phosphate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28673,T3D1351,Ethylmercuric phosphate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28674,T3D1351,Ethylmercuric phosphate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28675,T3D1351,Ethylmercuric phosphate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28676,T3D1351,Ethylmercuric phosphate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28677,T3D1351,Ethylmercuric phosphate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28678,T3D1351,Ethylmercuric phosphate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28679,T3D1351,Ethylmercuric phosphate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28680,T3D1351,Ethylmercuric phosphate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28681,T3D1352,Methoxyethelmercuric acetate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28682,T3D1352,Methoxyethelmercuric acetate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28683,T3D1352,Methoxyethelmercuric acetate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28684,T3D1352,Methoxyethelmercuric acetate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28685,T3D1352,Methoxyethelmercuric acetate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28686,T3D1352,Methoxyethelmercuric acetate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28687,T3D1352,Methoxyethelmercuric acetate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28688,T3D1352,Methoxyethelmercuric acetate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28689,T3D1352,Methoxyethelmercuric acetate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28690,T3D1352,Methoxyethelmercuric acetate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28691,T3D1352,Methoxyethelmercuric acetate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28692,T3D1352,Methoxyethelmercuric acetate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28693,T3D1352,Methoxyethelmercuric acetate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28694,T3D1352,Methoxyethelmercuric acetate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28695,T3D1352,Methoxyethelmercuric acetate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28696,T3D1352,Methoxyethelmercuric acetate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28697,T3D1352,Methoxyethelmercuric acetate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28698,T3D1352,Methoxyethelmercuric acetate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28699,T3D1352,Methoxyethelmercuric acetate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28700,T3D1352,Methoxyethelmercuric acetate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28701,T3D1352,Methoxyethelmercuric acetate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28702,T3D1352,Methoxyethelmercuric acetate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28703,T3D1352,Methoxyethelmercuric acetate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28704,T3D1352,Methoxyethelmercuric acetate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28705,T3D1352,Methoxyethelmercuric acetate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28706,T3D1352,Methoxyethelmercuric acetate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28707,T3D1352,Methoxyethelmercuric acetate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28708,T3D1352,Methoxyethelmercuric acetate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28709,T3D1352,Methoxyethelmercuric acetate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28710,T3D1352,Methoxyethelmercuric acetate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28711,T3D1352,Methoxyethelmercuric acetate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28712,T3D1352,Methoxyethelmercuric acetate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28713,T3D1352,Methoxyethelmercuric acetate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28714,T3D1352,Methoxyethelmercuric acetate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28715,T3D1352,Methoxyethelmercuric acetate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28716,T3D1352,Methoxyethelmercuric acetate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28717,T3D1352,Methoxyethelmercuric acetate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28718,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28719,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28720,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28721,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28722,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28723,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28724,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28725,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28726,T3D1352,Methoxyethelmercuric acetate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28727,T3D1352,Methoxyethelmercuric acetate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28728,T3D1352,Methoxyethelmercuric acetate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28729,T3D1352,Methoxyethelmercuric acetate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28730,T3D1352,Methoxyethelmercuric acetate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28731,T3D1353,Ethoxyethyl hydroxy mercury,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28732,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28733,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28734,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28735,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28736,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28737,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28738,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28739,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28740,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28741,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28742,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28743,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28744,T3D1353,Ethoxyethyl hydroxy mercury,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28745,T3D1353,Ethoxyethyl hydroxy mercury,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28746,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28747,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28748,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28749,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28750,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28751,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28752,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28753,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28754,T3D1353,Ethoxyethyl hydroxy mercury,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28755,T3D1353,Ethoxyethyl hydroxy mercury,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28756,T3D1353,Ethoxyethyl hydroxy mercury,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28757,T3D1353,Ethoxyethyl hydroxy mercury,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28758,T3D1353,Ethoxyethyl hydroxy mercury,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28759,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28760,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28761,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28762,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28763,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28764,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28765,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28766,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28767,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28768,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28769,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28770,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28771,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28772,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28773,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28774,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28775,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28776,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28777,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28778,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28779,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28780,T3D1353,Ethoxyethyl hydroxy mercury,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28781,T3D1354,Phenylmercuric chloride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28782,T3D1354,Phenylmercuric chloride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28783,T3D1354,Phenylmercuric chloride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28784,T3D1354,Phenylmercuric chloride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28785,T3D1354,Phenylmercuric chloride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28786,T3D1354,Phenylmercuric chloride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28787,T3D1354,Phenylmercuric chloride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28788,T3D1354,Phenylmercuric chloride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28789,T3D1354,Phenylmercuric chloride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28790,T3D1354,Phenylmercuric chloride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28791,T3D1354,Phenylmercuric chloride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28792,T3D1354,Phenylmercuric chloride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28793,T3D1354,Phenylmercuric chloride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28794,T3D1354,Phenylmercuric chloride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28795,T3D1354,Phenylmercuric chloride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28796,T3D1354,Phenylmercuric chloride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28797,T3D1354,Phenylmercuric chloride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28798,T3D1354,Phenylmercuric chloride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28799,T3D1354,Phenylmercuric chloride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28800,T3D1354,Phenylmercuric chloride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28801,T3D1354,Phenylmercuric chloride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28802,T3D1354,Phenylmercuric chloride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28803,T3D1354,Phenylmercuric chloride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28804,T3D1354,Phenylmercuric chloride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28805,T3D1354,Phenylmercuric chloride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28806,T3D1354,Phenylmercuric chloride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28807,T3D1354,Phenylmercuric chloride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28808,T3D1354,Phenylmercuric chloride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28809,T3D1354,Phenylmercuric chloride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28810,T3D1354,Phenylmercuric chloride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28811,T3D1354,Phenylmercuric chloride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28812,T3D1354,Phenylmercuric chloride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28813,T3D1354,Phenylmercuric chloride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28814,T3D1354,Phenylmercuric chloride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28815,T3D1354,Phenylmercuric chloride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28816,T3D1354,Phenylmercuric chloride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28817,T3D1354,Phenylmercuric chloride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28818,T3D1354,Phenylmercuric chloride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28819,T3D1354,Phenylmercuric chloride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28820,T3D1354,Phenylmercuric chloride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28821,T3D1354,Phenylmercuric chloride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28822,T3D1354,Phenylmercuric chloride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28823,T3D1354,Phenylmercuric chloride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28824,T3D1354,Phenylmercuric chloride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28825,T3D1354,Phenylmercuric chloride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28826,T3D1354,Phenylmercuric chloride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28827,T3D1354,Phenylmercuric chloride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28828,T3D1354,Phenylmercuric chloride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28829,T3D1354,Phenylmercuric chloride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28830,T3D1354,Phenylmercuric chloride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28831,T3D1355,Phenylmercuric nitrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28832,T3D1355,Phenylmercuric nitrate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28833,T3D1355,Phenylmercuric nitrate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28834,T3D1355,Phenylmercuric nitrate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28835,T3D1355,Phenylmercuric nitrate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28836,T3D1355,Phenylmercuric nitrate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28837,T3D1355,Phenylmercuric nitrate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28838,T3D1355,Phenylmercuric nitrate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28839,T3D1355,Phenylmercuric nitrate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28840,T3D1355,Phenylmercuric nitrate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28841,T3D1355,Phenylmercuric nitrate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28842,T3D1355,Phenylmercuric nitrate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28843,T3D1355,Phenylmercuric nitrate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28844,T3D1355,Phenylmercuric nitrate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28845,T3D1355,Phenylmercuric nitrate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28846,T3D1355,Phenylmercuric nitrate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28847,T3D1355,Phenylmercuric nitrate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28848,T3D1355,Phenylmercuric nitrate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28849,T3D1355,Phenylmercuric nitrate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28850,T3D1355,Phenylmercuric nitrate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28851,T3D1355,Phenylmercuric nitrate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28852,T3D1355,Phenylmercuric nitrate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28853,T3D1355,Phenylmercuric nitrate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28854,T3D1355,Phenylmercuric nitrate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28855,T3D1355,Phenylmercuric nitrate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28856,T3D1355,Phenylmercuric nitrate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28857,T3D1355,Phenylmercuric nitrate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28858,T3D1355,Phenylmercuric nitrate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28859,T3D1355,Phenylmercuric nitrate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28860,T3D1355,Phenylmercuric nitrate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28861,T3D1355,Phenylmercuric nitrate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28862,T3D1355,Phenylmercuric nitrate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28863,T3D1355,Phenylmercuric nitrate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28864,T3D1355,Phenylmercuric nitrate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28865,T3D1355,Phenylmercuric nitrate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28866,T3D1355,Phenylmercuric nitrate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28867,T3D1355,Phenylmercuric nitrate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28868,T3D1355,Phenylmercuric nitrate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28869,T3D1355,Phenylmercuric nitrate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28870,T3D1355,Phenylmercuric nitrate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28871,T3D1355,Phenylmercuric nitrate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28872,T3D1355,Phenylmercuric nitrate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28873,T3D1355,Phenylmercuric nitrate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28874,T3D1355,Phenylmercuric nitrate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28875,T3D1355,Phenylmercuric nitrate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28876,T3D1355,Phenylmercuric nitrate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28877,T3D1355,Phenylmercuric nitrate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28878,T3D1355,Phenylmercuric nitrate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28879,T3D1355,Phenylmercuric nitrate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28880,T3D1355,Phenylmercuric nitrate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28881,T3D1356,Mercurol,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28882,T3D1356,Mercurol,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28883,T3D1356,Mercurol,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28884,T3D1356,Mercurol,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28885,T3D1356,Mercurol,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28886,T3D1356,Mercurol,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28887,T3D1356,Mercurol,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28888,T3D1356,Mercurol,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28889,T3D1356,Mercurol,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28890,T3D1356,Mercurol,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28891,T3D1356,Mercurol,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28892,T3D1356,Mercurol,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28893,T3D1356,Mercurol,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28894,T3D1356,Mercurol,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28895,T3D1356,Mercurol,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28896,T3D1356,Mercurol,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28897,T3D1356,Mercurol,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28898,T3D1356,Mercurol,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28899,T3D1356,Mercurol,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28900,T3D1356,Mercurol,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28901,T3D1356,Mercurol,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28902,T3D1356,Mercurol,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28903,T3D1356,Mercurol,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28904,T3D1356,Mercurol,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28905,T3D1356,Mercurol,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28906,T3D1356,Mercurol,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28907,T3D1356,Mercurol,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28908,T3D1356,Mercurol,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28909,T3D1356,Mercurol,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28910,T3D1356,Mercurol,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28911,T3D1356,Mercurol,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28912,T3D1356,Mercurol,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28913,T3D1356,Mercurol,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28914,T3D1356,Mercurol,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28915,T3D1356,Mercurol,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28916,T3D1356,Mercurol,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28917,T3D1356,Mercurol,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28918,T3D1356,Mercurol,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28919,T3D1356,Mercurol,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28920,T3D1356,Mercurol,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28921,T3D1356,Mercurol,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28922,T3D1356,Mercurol,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28923,T3D1356,Mercurol,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28924,T3D1356,Mercurol,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28925,T3D1356,Mercurol,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28926,T3D1356,Mercurol,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28927,T3D1356,Mercurol,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28928,T3D1356,Mercurol,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28929,T3D1356,Mercurol,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28930,T3D1356,Mercurol,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28931,T3D1357,Mercaptomerin,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28932,T3D1357,Mercaptomerin,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28933,T3D1357,Mercaptomerin,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28934,T3D1357,Mercaptomerin,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28935,T3D1357,Mercaptomerin,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28936,T3D1357,Mercaptomerin,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28937,T3D1357,Mercaptomerin,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28938,T3D1357,Mercaptomerin,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28939,T3D1357,Mercaptomerin,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28940,T3D1357,Mercaptomerin,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28941,T3D1357,Mercaptomerin,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28942,T3D1357,Mercaptomerin,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28943,T3D1357,Mercaptomerin,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28944,T3D1357,Mercaptomerin,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28945,T3D1357,Mercaptomerin,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28946,T3D1357,Mercaptomerin,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28947,T3D1357,Mercaptomerin,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28948,T3D1357,Mercaptomerin,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28949,T3D1357,Mercaptomerin,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28950,T3D1357,Mercaptomerin,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28951,T3D1357,Mercaptomerin,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28952,T3D1357,Mercaptomerin,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28953,T3D1357,Mercaptomerin,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28954,T3D1357,Mercaptomerin,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28955,T3D1357,Mercaptomerin,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
28956,T3D1357,Mercaptomerin,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28957,T3D1357,Mercaptomerin,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28958,T3D1357,Mercaptomerin,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28959,T3D1357,Mercaptomerin,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28960,T3D1357,Mercaptomerin,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28961,T3D1357,Mercaptomerin,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28962,T3D1357,Mercaptomerin,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28963,T3D1357,Mercaptomerin,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28964,T3D1357,Mercaptomerin,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28965,T3D1357,Mercaptomerin,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28966,T3D1357,Mercaptomerin,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28967,T3D1357,Mercaptomerin,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28968,T3D1357,Mercaptomerin,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28969,T3D1357,Mercaptomerin,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28970,T3D1357,Mercaptomerin,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28971,T3D1357,Mercaptomerin,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28972,T3D1357,Mercaptomerin,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28973,T3D1357,Mercaptomerin,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28974,T3D1357,Mercaptomerin,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28975,T3D1357,Mercaptomerin,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28976,T3D1357,Mercaptomerin,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28977,T3D1357,Mercaptomerin,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28978,T3D1357,Mercaptomerin,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28979,T3D1357,Mercaptomerin,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28980,T3D1357,Mercaptomerin,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
28981,T3D1358,Diethyl mercury,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28982,T3D1358,Diethyl mercury,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28983,T3D1358,Diethyl mercury,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28984,T3D1358,Diethyl mercury,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28985,T3D1358,Diethyl mercury,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28986,T3D1358,Diethyl mercury,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28987,T3D1358,Diethyl mercury,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28988,T3D1358,Diethyl mercury,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28989,T3D1358,Diethyl mercury,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28990,T3D1358,Diethyl mercury,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28991,T3D1358,Diethyl mercury,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28992,T3D1358,Diethyl mercury,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28993,T3D1358,Diethyl mercury,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28994,T3D1358,Diethyl mercury,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28995,T3D1358,Diethyl mercury,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
28996,T3D1358,Diethyl mercury,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28997,T3D1358,Diethyl mercury,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28998,T3D1358,Diethyl mercury,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
28999,T3D1358,Diethyl mercury,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29000,T3D1358,Diethyl mercury,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29001,T3D1358,Diethyl mercury,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29002,T3D1358,Diethyl mercury,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29003,T3D1358,Diethyl mercury,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29004,T3D1358,Diethyl mercury,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29005,T3D1358,Diethyl mercury,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
29006,T3D1358,Diethyl mercury,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29007,T3D1358,Diethyl mercury,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29008,T3D1358,Diethyl mercury,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29009,T3D1358,Diethyl mercury,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29010,T3D1358,Diethyl mercury,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29011,T3D1358,Diethyl mercury,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29012,T3D1358,Diethyl mercury,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29013,T3D1358,Diethyl mercury,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29014,T3D1358,Diethyl mercury,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29015,T3D1358,Diethyl mercury,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29016,T3D1358,Diethyl mercury,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29017,T3D1358,Diethyl mercury,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29018,T3D1358,Diethyl mercury,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29019,T3D1358,Diethyl mercury,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29020,T3D1358,Diethyl mercury,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29021,T3D1358,Diethyl mercury,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29022,T3D1358,Diethyl mercury,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29023,T3D1358,Diethyl mercury,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29024,T3D1358,Diethyl mercury,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29025,T3D1358,Diethyl mercury,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29026,T3D1358,Diethyl mercury,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29027,T3D1358,Diethyl mercury,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29028,T3D1358,Diethyl mercury,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29029,T3D1358,Diethyl mercury,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29030,T3D1358,Diethyl mercury,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29031,T3D1359,Ethylmercury chloride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29032,T3D1359,Ethylmercury chloride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29033,T3D1359,Ethylmercury chloride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29034,T3D1359,Ethylmercury chloride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29035,T3D1359,Ethylmercury chloride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29036,T3D1359,Ethylmercury chloride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29037,T3D1359,Ethylmercury chloride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29038,T3D1359,Ethylmercury chloride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29039,T3D1359,Ethylmercury chloride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29040,T3D1359,Ethylmercury chloride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29041,T3D1359,Ethylmercury chloride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29042,T3D1359,Ethylmercury chloride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29043,T3D1359,Ethylmercury chloride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29044,T3D1359,Ethylmercury chloride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29045,T3D1359,Ethylmercury chloride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29046,T3D1359,Ethylmercury chloride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29047,T3D1359,Ethylmercury chloride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29048,T3D1359,Ethylmercury chloride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29049,T3D1359,Ethylmercury chloride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29050,T3D1359,Ethylmercury chloride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29051,T3D1359,Ethylmercury chloride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29052,T3D1359,Ethylmercury chloride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29053,T3D1359,Ethylmercury chloride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29054,T3D1359,Ethylmercury chloride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29055,T3D1359,Ethylmercury chloride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
29056,T3D1359,Ethylmercury chloride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29057,T3D1359,Ethylmercury chloride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29058,T3D1359,Ethylmercury chloride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29059,T3D1359,Ethylmercury chloride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29060,T3D1359,Ethylmercury chloride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29061,T3D1359,Ethylmercury chloride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29062,T3D1359,Ethylmercury chloride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29063,T3D1359,Ethylmercury chloride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29064,T3D1359,Ethylmercury chloride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29065,T3D1359,Ethylmercury chloride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29066,T3D1359,Ethylmercury chloride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29067,T3D1359,Ethylmercury chloride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29068,T3D1359,Ethylmercury chloride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29069,T3D1359,Ethylmercury chloride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29070,T3D1359,Ethylmercury chloride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29071,T3D1359,Ethylmercury chloride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29072,T3D1359,Ethylmercury chloride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29073,T3D1359,Ethylmercury chloride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29074,T3D1359,Ethylmercury chloride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29075,T3D1359,Ethylmercury chloride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29076,T3D1359,Ethylmercury chloride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29077,T3D1359,Ethylmercury chloride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29078,T3D1359,Ethylmercury chloride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29079,T3D1359,Ethylmercury chloride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29080,T3D1359,Ethylmercury chloride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29081,T3D1360,Meralluride,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29082,T3D1360,Meralluride,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29083,T3D1360,Meralluride,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29084,T3D1360,Meralluride,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29085,T3D1360,Meralluride,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29086,T3D1360,Meralluride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29087,T3D1360,Meralluride,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29088,T3D1360,Meralluride,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29089,T3D1360,Meralluride,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29090,T3D1360,Meralluride,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29091,T3D1360,Meralluride,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29092,T3D1360,Meralluride,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29093,T3D1360,Meralluride,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29094,T3D1360,Meralluride,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29095,T3D1360,Meralluride,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29096,T3D1360,Meralluride,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29097,T3D1360,Meralluride,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29098,T3D1360,Meralluride,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29099,T3D1360,Meralluride,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29100,T3D1360,Meralluride,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29101,T3D1360,Meralluride,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29102,T3D1360,Meralluride,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29103,T3D1360,Meralluride,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29104,T3D1360,Meralluride,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29105,T3D1360,Meralluride,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
29106,T3D1360,Meralluride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29107,T3D1360,Meralluride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29108,T3D1360,Meralluride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29109,T3D1360,Meralluride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29110,T3D1360,Meralluride,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29111,T3D1360,Meralluride,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29112,T3D1360,Meralluride,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29113,T3D1360,Meralluride,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29114,T3D1360,Meralluride,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29115,T3D1360,Meralluride,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29116,T3D1360,Meralluride,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29117,T3D1360,Meralluride,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29118,T3D1360,Meralluride,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29119,T3D1360,Meralluride,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29120,T3D1360,Meralluride,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29121,T3D1360,Meralluride,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29122,T3D1360,Meralluride,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29123,T3D1360,Meralluride,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29124,T3D1360,Meralluride,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29125,T3D1360,Meralluride,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29126,T3D1360,Meralluride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29127,T3D1360,Meralluride,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29128,T3D1360,Meralluride,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29129,T3D1360,Meralluride,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29130,T3D1360,Meralluride,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29131,T3D1361,Merbromin,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29132,T3D1361,Merbromin,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29133,T3D1361,Merbromin,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29134,T3D1361,Merbromin,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29135,T3D1361,Merbromin,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29136,T3D1361,Merbromin,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29137,T3D1361,Merbromin,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29138,T3D1361,Merbromin,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29139,T3D1361,Merbromin,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29140,T3D1361,Merbromin,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29141,T3D1361,Merbromin,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29142,T3D1361,Merbromin,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29143,T3D1361,Merbromin,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29144,T3D1361,Merbromin,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29145,T3D1361,Merbromin,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29146,T3D1361,Merbromin,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29147,T3D1361,Merbromin,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29148,T3D1361,Merbromin,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29149,T3D1361,Merbromin,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29150,T3D1361,Merbromin,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29151,T3D1361,Merbromin,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29152,T3D1361,Merbromin,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29153,T3D1361,Merbromin,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29154,T3D1361,Merbromin,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29155,T3D1361,Merbromin,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
29156,T3D1361,Merbromin,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29157,T3D1361,Merbromin,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29158,T3D1361,Merbromin,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29159,T3D1361,Merbromin,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29160,T3D1361,Merbromin,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29161,T3D1361,Merbromin,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29162,T3D1361,Merbromin,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29163,T3D1361,Merbromin,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29164,T3D1361,Merbromin,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29165,T3D1361,Merbromin,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29166,T3D1361,Merbromin,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29167,T3D1361,Merbromin,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29168,T3D1361,Merbromin,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29169,T3D1361,Merbromin,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29170,T3D1361,Merbromin,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29171,T3D1361,Merbromin,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29172,T3D1361,Merbromin,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29173,T3D1361,Merbromin,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29174,T3D1361,Merbromin,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29175,T3D1361,Merbromin,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29176,T3D1361,Merbromin,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29177,T3D1361,Merbromin,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29178,T3D1361,Merbromin,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29179,T3D1361,Merbromin,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29180,T3D1361,Merbromin,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29181,T3D1362,Mersalyl acid,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29182,T3D1362,Mersalyl acid,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29183,T3D1362,Mersalyl acid,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29184,T3D1362,Mersalyl acid,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29185,T3D1362,Mersalyl acid,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29186,T3D1362,Mersalyl acid,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29187,T3D1362,Mersalyl acid,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29188,T3D1362,Mersalyl acid,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29189,T3D1362,Mersalyl acid,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29190,T3D1362,Mersalyl acid,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29191,T3D1362,Mersalyl acid,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29192,T3D1362,Mersalyl acid,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29193,T3D1362,Mersalyl acid,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29194,T3D1362,Mersalyl acid,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29195,T3D1362,Mersalyl acid,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29196,T3D1362,Mersalyl acid,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29197,T3D1362,Mersalyl acid,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29198,T3D1362,Mersalyl acid,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29199,T3D1362,Mersalyl acid,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29200,T3D1362,Mersalyl acid,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29201,T3D1362,Mersalyl acid,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29202,T3D1362,Mersalyl acid,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29203,T3D1362,Mersalyl acid,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29204,T3D1362,Mersalyl acid,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29205,T3D1362,Mersalyl acid,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
29206,T3D1362,Mersalyl acid,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29207,T3D1362,Mersalyl acid,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29208,T3D1362,Mersalyl acid,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29209,T3D1362,Mersalyl acid,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29210,T3D1362,Mersalyl acid,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29211,T3D1362,Mersalyl acid,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29212,T3D1362,Mersalyl acid,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29213,T3D1362,Mersalyl acid,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29214,T3D1362,Mersalyl acid,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29215,T3D1362,Mersalyl acid,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29216,T3D1362,Mersalyl acid,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29217,T3D1362,Mersalyl acid,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29218,T3D1362,Mersalyl acid,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29219,T3D1362,Mersalyl acid,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29220,T3D1362,Mersalyl acid,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29221,T3D1362,Mersalyl acid,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29222,T3D1362,Mersalyl acid,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29223,T3D1362,Mersalyl acid,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29224,T3D1362,Mersalyl acid,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29225,T3D1362,Mersalyl acid,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29226,T3D1362,Mersalyl acid,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29227,T3D1362,Mersalyl acid,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29228,T3D1362,Mersalyl acid,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29229,T3D1362,Mersalyl acid,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29230,T3D1362,Mersalyl acid,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29231,T3D1363,Phenylmercuric borate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29232,T3D1363,Phenylmercuric borate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29233,T3D1363,Phenylmercuric borate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29234,T3D1363,Phenylmercuric borate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29235,T3D1363,Phenylmercuric borate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29236,T3D1363,Phenylmercuric borate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29237,T3D1363,Phenylmercuric borate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29238,T3D1363,Phenylmercuric borate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29239,T3D1363,Phenylmercuric borate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29240,T3D1363,Phenylmercuric borate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29241,T3D1363,Phenylmercuric borate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29242,T3D1363,Phenylmercuric borate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29243,T3D1363,Phenylmercuric borate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29244,T3D1363,Phenylmercuric borate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29245,T3D1363,Phenylmercuric borate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29246,T3D1363,Phenylmercuric borate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29247,T3D1363,Phenylmercuric borate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29248,T3D1363,Phenylmercuric borate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29249,T3D1363,Phenylmercuric borate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29250,T3D1363,Phenylmercuric borate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29251,T3D1363,Phenylmercuric borate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29252,T3D1363,Phenylmercuric borate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29253,T3D1363,Phenylmercuric borate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29254,T3D1363,Phenylmercuric borate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29255,T3D1363,Phenylmercuric borate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
29256,T3D1363,Phenylmercuric borate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29257,T3D1363,Phenylmercuric borate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29258,T3D1363,Phenylmercuric borate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29259,T3D1363,Phenylmercuric borate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29260,T3D1363,Phenylmercuric borate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29261,T3D1363,Phenylmercuric borate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29262,T3D1363,Phenylmercuric borate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29263,T3D1363,Phenylmercuric borate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29264,T3D1363,Phenylmercuric borate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29265,T3D1363,Phenylmercuric borate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29266,T3D1363,Phenylmercuric borate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29267,T3D1363,Phenylmercuric borate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29268,T3D1363,Phenylmercuric borate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29269,T3D1363,Phenylmercuric borate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29270,T3D1363,Phenylmercuric borate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29271,T3D1363,Phenylmercuric borate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29272,T3D1363,Phenylmercuric borate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29273,T3D1363,Phenylmercuric borate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29274,T3D1363,Phenylmercuric borate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29275,T3D1363,Phenylmercuric borate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29276,T3D1363,Phenylmercuric borate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29277,T3D1363,Phenylmercuric borate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29278,T3D1363,Phenylmercuric borate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29279,T3D1363,Phenylmercuric borate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29280,T3D1363,Phenylmercuric borate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29281,T3D1364,Thiomersal,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29282,T3D1364,Thiomersal,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29283,T3D1364,Thiomersal,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29284,T3D1364,Thiomersal,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29285,T3D1364,Thiomersal,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29286,T3D1364,Thiomersal,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29287,T3D1364,Thiomersal,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29288,T3D1364,Thiomersal,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29289,T3D1364,Thiomersal,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29290,T3D1364,Thiomersal,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29291,T3D1364,Thiomersal,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29292,T3D1364,Thiomersal,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29293,T3D1364,Thiomersal,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29294,T3D1364,Thiomersal,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29295,T3D1364,Thiomersal,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29296,T3D1364,Thiomersal,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29297,T3D1364,Thiomersal,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29298,T3D1364,Thiomersal,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29299,T3D1364,Thiomersal,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29300,T3D1364,Thiomersal,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29301,T3D1364,Thiomersal,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29302,T3D1364,Thiomersal,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29303,T3D1364,Thiomersal,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29304,T3D1364,Thiomersal,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29305,T3D1364,Thiomersal,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
29306,T3D1364,Thiomersal,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29307,T3D1364,Thiomersal,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29308,T3D1364,Thiomersal,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29309,T3D1364,Thiomersal,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29310,T3D1364,Thiomersal,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29311,T3D1364,Thiomersal,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29312,T3D1364,Thiomersal,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29313,T3D1364,Thiomersal,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29314,T3D1364,Thiomersal,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29315,T3D1364,Thiomersal,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29316,T3D1364,Thiomersal,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29317,T3D1364,Thiomersal,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29318,T3D1364,Thiomersal,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29319,T3D1364,Thiomersal,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29320,T3D1364,Thiomersal,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29321,T3D1364,Thiomersal,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29322,T3D1364,Thiomersal,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29323,T3D1364,Thiomersal,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29324,T3D1364,Thiomersal,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29325,T3D1364,Thiomersal,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29326,T3D1364,Thiomersal,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29327,T3D1364,Thiomersal,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29328,T3D1364,Thiomersal,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29329,T3D1364,Thiomersal,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29330,T3D1364,Thiomersal,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29331,T3D1365,Mercury(II) nitrate hydrate,"Alkaline phosphatase, tissue-nonspecific isozyme",P05186,"Mercury affects the nervous system by inhibiting alkaline phosphatase, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29332,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-1,P29972,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29333,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-10,Q96PS8,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29334,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-11,Q8NBQ7,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29335,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-12A,Q8IXF9,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29336,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29337,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-2,P41181,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29338,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-3,Q92482,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29339,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-4,P55087,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29340,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-5,P55064,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29341,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-6,Q13520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29342,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-7,O14520,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29343,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-8,O94778,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29344,T3D1365,Mercury(II) nitrate hydrate,Aquaporin-9,O43315,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29345,T3D1365,Mercury(II) nitrate hydrate,Lens fiber major intrinsic protein,P30301,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29346,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C alpha type,P17252,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29347,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C beta type,P05771,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29348,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C delta type,Q05655,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29349,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C epsilon type,Q02156,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29350,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C eta type,P24723,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29351,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C gamma type,P05129,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29352,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C iota type,P41743,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29353,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C theta type,Q04759,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29354,T3D1365,Mercury(II) nitrate hydrate,Protein kinase C zeta type,Q05513,"Mercury affects the nervous system by inhibiting protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. (R022)"
29355,T3D1365,Mercury(II) nitrate hydrate,Proto-oncogene tyrosine-protein kinase LCK,P06239,"Mercury inhibits the protein LCK, which causes decreased T-cell signalling and immune system depression. (R066)"
29356,T3D1365,Mercury(II) nitrate hydrate,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29357,T3D1365,Mercury(II) nitrate hydrate,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29358,T3D1365,Mercury(II) nitrate hydrate,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29359,T3D1365,Mercury(II) nitrate hydrate,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29360,T3D1365,Mercury(II) nitrate hydrate,Tubulin alpha-1A chain,Q71U36,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29361,T3D1365,Mercury(II) nitrate hydrate,Tubulin alpha-1B chain,P68363,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29362,T3D1365,Mercury(II) nitrate hydrate,Tubulin alpha-1C chain,Q9BQE3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29363,T3D1365,Mercury(II) nitrate hydrate,Tubulin alpha-3C/D chain,Q13748,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29364,T3D1365,Mercury(II) nitrate hydrate,Tubulin alpha-3E chain,Q6PEY2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29365,T3D1365,Mercury(II) nitrate hydrate,Tubulin alpha-4A chain,P68366,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29366,T3D1365,Mercury(II) nitrate hydrate,Tubulin alpha-8 chain,Q9NY65,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29367,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta chain,P07437,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29368,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-1 chain,Q9H4B7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29369,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-2A chain,Q13885,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29370,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-2B chain,Q9BVA1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29371,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-2C chain,P68371,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29372,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-3 chain,Q13509,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29373,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-4 chain,P04350,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29374,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-6 chain,Q9BUF5,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29375,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-8 chain,Q3ZCM7,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29376,T3D1365,Mercury(II) nitrate hydrate,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29377,T3D1365,Mercury(II) nitrate hydrate,Tubulin delta chain,Q9UJT1,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29378,T3D1365,Mercury(II) nitrate hydrate,Tubulin epsilon chain,Q9UJT0,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29379,T3D1365,Mercury(II) nitrate hydrate,Tubulin gamma-1 chain,P23258,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29380,T3D1365,Mercury(II) nitrate hydrate,Tubulin gamma-2 chain,Q9NRH3,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29381,T3D0242,Mercuric chloride,Aquaporin-12B,A6NM10,"Mercury is known to inhibit aquaporins, halting water flow across the cell membrane and resulting in cell injury and death. (R067)"
29382,T3D0242,Mercuric chloride,Putative tubulin beta chain-like protein ENSP00000290377,A6NKZ8 ,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29383,T3D0242,Mercuric chloride,Putative tubulin beta-4q chain,Q99867,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29384,T3D0242,Mercuric chloride,Putative tubulin-like protein alpha-4B,Q9H853,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29385,T3D0242,Mercuric chloride,Tubulin alpha chain-like 3,A6NHL2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29386,T3D0242,Mercuric chloride,Tubulin beta-8 chain B,A6NNZ2,"Organic mercury exerts developmental effects by binding to tubulin, preventing microtubule assembly and causing mitotic inhibition. (R022)"
29387,T3D0365,Cadmium acetate hydrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29388,T3D0365,Cadmium acetate hydrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29389,T3D0365,Cadmium acetate hydrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29390,T3D0365,Cadmium acetate hydrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29391,T3D0365,Cadmium acetate hydrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29392,T3D0365,Cadmium acetate hydrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29393,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29394,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29395,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29396,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29397,T3D0365,Cadmium acetate hydrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29398,T3D0366,Cadmium acetate dihydrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29399,T3D0366,Cadmium acetate dihydrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29400,T3D0366,Cadmium acetate dihydrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29401,T3D0366,Cadmium acetate dihydrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29402,T3D0366,Cadmium acetate dihydrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29403,T3D0366,Cadmium acetate dihydrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29404,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29405,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29406,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29407,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29408,T3D0366,Cadmium acetate dihydrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29409,T3D0367,Cadmium arsenide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29410,T3D0367,Cadmium arsenide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29411,T3D0367,Cadmium arsenide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29412,T3D0367,Cadmium arsenide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29413,T3D0367,Cadmium arsenide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29414,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29415,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29416,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29417,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29418,T3D0367,Cadmium arsenide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29419,T3D0368,Cadmium bromate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29420,T3D0368,Cadmium bromate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29421,T3D0368,Cadmium bromate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29422,T3D0368,Cadmium bromate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29423,T3D0368,Cadmium bromate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29424,T3D0368,Cadmium bromate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29425,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29426,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29427,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29428,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29429,T3D0368,Cadmium bromate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29430,T3D0369,Cadmium bromide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29431,T3D0369,Cadmium bromide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29432,T3D0369,Cadmium bromide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29433,T3D0369,Cadmium bromide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29434,T3D0369,Cadmium bromide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29435,T3D0369,Cadmium bromide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29436,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29437,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29438,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29439,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29440,T3D0369,Cadmium bromide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29441,T3D0370,Cadmium carbonate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29442,T3D0370,Cadmium carbonate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29443,T3D0370,Cadmium carbonate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29444,T3D0370,Cadmium carbonate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29445,T3D0370,Cadmium carbonate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29446,T3D0370,Cadmium carbonate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29447,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29448,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29449,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29450,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29451,T3D0370,Cadmium carbonate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29452,T3D0371,Cadmium chloride,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29453,T3D0371,Cadmium chloride,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29454,T3D0371,Cadmium chloride,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29455,T3D0371,Cadmium chloride,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29456,T3D0371,Cadmium chloride,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29457,T3D0371,Cadmium chloride,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29458,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29459,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29460,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29461,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29462,T3D0371,Cadmium chloride,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29463,T3D0372,Cadmium fluoborate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29464,T3D0372,Cadmium fluoborate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29465,T3D0372,Cadmium fluoborate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29466,T3D0372,Cadmium fluoborate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29467,T3D0372,Cadmium fluoborate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29468,T3D0372,Cadmium fluoborate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29469,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29470,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29471,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29472,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29473,T3D0372,Cadmium fluoborate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29474,T3D0373,Cadmium fluoride,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29475,T3D0373,Cadmium fluoride,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29476,T3D0373,Cadmium fluoride,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29477,T3D0373,Cadmium fluoride,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29478,T3D0373,Cadmium fluoride,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29479,T3D0373,Cadmium fluoride,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29480,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29481,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29482,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29483,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29484,T3D0373,Cadmium fluoride,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29485,T3D0374,Cadmium fluosilicate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29486,T3D0374,Cadmium fluosilicate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29487,T3D0374,Cadmium fluosilicate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29488,T3D0374,Cadmium fluosilicate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29489,T3D0374,Cadmium fluosilicate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29490,T3D0374,Cadmium fluosilicate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29491,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29492,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29493,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29494,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29495,T3D0374,Cadmium fluosilicate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29496,T3D0375,Cadmium hydroxide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29497,T3D0375,Cadmium hydroxide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29498,T3D0375,Cadmium hydroxide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29499,T3D0375,Cadmium hydroxide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29500,T3D0375,Cadmium hydroxide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29501,T3D0375,Cadmium hydroxide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29502,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29503,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29504,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29505,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29506,T3D0375,Cadmium hydroxide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29507,T3D0376,Cadmium iodide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29508,T3D0376,Cadmium iodide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29509,T3D0376,Cadmium iodide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29510,T3D0376,Cadmium iodide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29511,T3D0376,Cadmium iodide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29512,T3D0376,Cadmium iodide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29513,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29514,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29515,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29516,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29517,T3D0376,Cadmium iodide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29518,T3D0377,Cadmium lactate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29519,T3D0377,Cadmium lactate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29520,T3D0377,Cadmium lactate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29521,T3D0377,Cadmium lactate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29522,T3D0377,Cadmium lactate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29523,T3D0377,Cadmium lactate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29524,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29525,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29526,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29527,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29528,T3D0377,Cadmium lactate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29529,T3D0378,Cadmium nitrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29530,T3D0378,Cadmium nitrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29531,T3D0378,Cadmium nitrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29532,T3D0378,Cadmium nitrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29533,T3D0378,Cadmium nitrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29534,T3D0378,Cadmium nitrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29535,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29536,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29537,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29538,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29539,T3D0378,Cadmium nitrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29540,T3D0379,Cadmium nitrate tetrahydrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29541,T3D0379,Cadmium nitrate tetrahydrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29542,T3D0379,Cadmium nitrate tetrahydrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29543,T3D0379,Cadmium nitrate tetrahydrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29544,T3D0379,Cadmium nitrate tetrahydrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29545,T3D0379,Cadmium nitrate tetrahydrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29546,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29547,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29548,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29549,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29550,T3D0379,Cadmium nitrate tetrahydrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29551,T3D0380,Cadmium oxide fume,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29552,T3D0380,Cadmium oxide fume,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29553,T3D0380,Cadmium oxide fume,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29554,T3D0380,Cadmium oxide fume,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29555,T3D0380,Cadmium oxide fume,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29556,T3D0380,Cadmium oxide fume,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29557,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29558,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29559,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29560,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29561,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29562,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29563,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29564,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29565,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29566,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29567,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29568,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29569,T3D0380,Cadmium oxide fume,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29570,T3D0381,Cadmium phosphate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29571,T3D0381,Cadmium phosphate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29572,T3D0381,Cadmium phosphate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29573,T3D0381,Cadmium phosphate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29574,T3D0381,Cadmium phosphate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29575,T3D0381,Cadmium phosphate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29576,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29577,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29578,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29579,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29580,T3D0381,Cadmium phosphate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29581,T3D0382,Cadmium selenide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29582,T3D0382,Cadmium selenide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29583,T3D0382,Cadmium selenide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29584,T3D0382,Cadmium selenide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29585,T3D0382,Cadmium selenide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29586,T3D0382,Cadmium selenide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29587,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29588,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29589,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29590,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29591,T3D0382,Cadmium selenide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29592,T3D0383,Cadmium succinate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29593,T3D0383,Cadmium succinate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29594,T3D0383,Cadmium succinate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29595,T3D0383,Cadmium succinate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29596,T3D0383,Cadmium succinate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29597,T3D0383,Cadmium succinate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29598,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29599,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29600,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29601,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29602,T3D0383,Cadmium succinate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29603,T3D0384,Cadmium sulfate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29604,T3D0384,Cadmium sulfate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29605,T3D0384,Cadmium sulfate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29606,T3D0384,Cadmium sulfate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29607,T3D0384,Cadmium sulfate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29608,T3D0384,Cadmium sulfate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29609,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29610,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29611,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29612,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29613,T3D0384,Cadmium sulfate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29614,T3D0385,Cadmium sulfate hydrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29615,T3D0385,Cadmium sulfate hydrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29616,T3D0385,Cadmium sulfate hydrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29617,T3D0385,Cadmium sulfate hydrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29618,T3D0385,Cadmium sulfate hydrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29619,T3D0385,Cadmium sulfate hydrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29620,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29621,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29622,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29623,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29624,T3D0385,Cadmium sulfate hydrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29625,T3D0386,Cadmium sulphide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29626,T3D0386,Cadmium sulphide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29627,T3D0386,Cadmium sulphide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29628,T3D0386,Cadmium sulphide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29629,T3D0386,Cadmium sulphide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29630,T3D0386,Cadmium sulphide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29631,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29632,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29633,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29634,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29635,T3D0386,Cadmium sulphide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29636,T3D0387,Cadmium telluride,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29637,T3D0387,Cadmium telluride,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29638,T3D0387,Cadmium telluride,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29639,T3D0387,Cadmium telluride,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29640,T3D0387,Cadmium telluride,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29641,T3D0387,Cadmium telluride,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29642,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29643,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29644,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29645,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29646,T3D0387,Cadmium telluride,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29647,T3D0388,Cadmium tungstate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29648,T3D0388,Cadmium tungstate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29649,T3D0388,Cadmium tungstate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29650,T3D0388,Cadmium tungstate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29651,T3D0388,Cadmium tungstate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29652,T3D0388,Cadmium tungstate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29653,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29654,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29655,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29656,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29657,T3D0388,Cadmium tungstate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29658,T3D1097,Barium cadmium stearate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29659,T3D1097,Barium cadmium stearate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29660,T3D1097,Barium cadmium stearate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29661,T3D1097,Barium cadmium stearate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29662,T3D1097,Barium cadmium stearate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29663,T3D1097,Barium cadmium stearate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29664,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29665,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29666,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29667,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29668,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29669,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29670,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29671,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29672,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29673,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29674,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29675,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29676,T3D1097,Barium cadmium stearate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29677,T3D1346,Cadmium mercury sulfide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29678,T3D1346,Cadmium mercury sulfide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29679,T3D1346,Cadmium mercury sulfide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29680,T3D1346,Cadmium mercury sulfide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29681,T3D1346,Cadmium mercury sulfide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29682,T3D1346,Cadmium mercury sulfide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29683,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29684,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29685,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29686,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29687,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29688,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29689,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29690,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29691,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29692,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29693,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29694,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29695,T3D1346,Cadmium mercury sulfide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29696,T3D1366,Cadmium chloride hemi-pentahydrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29697,T3D1366,Cadmium chloride hemi-pentahydrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29698,T3D1366,Cadmium chloride hemi-pentahydrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29699,T3D1366,Cadmium chloride hemi-pentahydrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29700,T3D1366,Cadmium chloride hemi-pentahydrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29701,T3D1366,Cadmium chloride hemi-pentahydrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29702,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29703,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29704,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29705,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29706,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29707,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29708,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29709,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29710,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29711,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29712,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29713,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29714,T3D1366,Cadmium chloride hemi-pentahydrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29715,T3D1367,Cadmium cyclohexane-butyrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29716,T3D1367,Cadmium cyclohexane-butyrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29717,T3D1367,Cadmium cyclohexane-butyrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29718,T3D1367,Cadmium cyclohexane-butyrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29719,T3D1367,Cadmium cyclohexane-butyrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29720,T3D1367,Cadmium cyclohexane-butyrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29721,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29722,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29723,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29724,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29725,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29726,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29727,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29728,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29729,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29730,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29731,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29732,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29733,T3D1367,Cadmium cyclohexane-butyrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29734,T3D1368,Cadmium sulfate monohydrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29735,T3D1368,Cadmium sulfate monohydrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29736,T3D1368,Cadmium sulfate monohydrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29737,T3D1368,Cadmium sulfate monohydrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29738,T3D1368,Cadmium sulfate monohydrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29739,T3D1368,Cadmium sulfate monohydrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29740,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29741,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29742,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29743,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29744,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29745,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29746,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29747,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29748,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29749,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29750,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29751,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29752,T3D1368,Cadmium sulfate monohydrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29753,T3D1369,Cadmium sulfate tetrahydrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29754,T3D1369,Cadmium sulfate tetrahydrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29755,T3D1369,Cadmium sulfate tetrahydrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29756,T3D1369,Cadmium sulfate tetrahydrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29757,T3D1369,Cadmium sulfate tetrahydrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29758,T3D1369,Cadmium sulfate tetrahydrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29759,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29760,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29761,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29762,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29763,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29764,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29765,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29766,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29767,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29768,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29769,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29770,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29771,T3D1369,Cadmium sulfate tetrahydrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29772,T3D1370,Cadmium sulfate octahydrate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29773,T3D1370,Cadmium sulfate octahydrate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29774,T3D1370,Cadmium sulfate octahydrate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29775,T3D1370,Cadmium sulfate octahydrate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29776,T3D1370,Cadmium sulfate octahydrate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29777,T3D1370,Cadmium sulfate octahydrate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29778,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29779,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29780,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29781,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29782,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29783,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29784,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29785,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29786,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29787,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29788,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29789,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29790,T3D1370,Cadmium sulfate octahydrate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29791,T3D1371,Cadmium 3-ethylhexanoate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29792,T3D1371,Cadmium 3-ethylhexanoate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29793,T3D1371,Cadmium 3-ethylhexanoate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29794,T3D1371,Cadmium 3-ethylhexanoate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29795,T3D1371,Cadmium 3-ethylhexanoate,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29796,T3D1371,Cadmium 3-ethylhexanoate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29797,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29798,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29799,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29800,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29801,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29802,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29803,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29804,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29805,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29806,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29807,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29808,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29809,T3D1371,Cadmium 3-ethylhexanoate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29810,T3D1372,Cadmium cyanide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29811,T3D1372,Cadmium cyanide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29812,T3D1372,Cadmium cyanide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29813,T3D1372,Cadmium cyanide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29814,T3D1372,Cadmium cyanide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29815,T3D1372,Cadmium cyanide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29816,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29817,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29818,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29819,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29820,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29821,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29822,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29823,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29824,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29825,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29826,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29827,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29828,T3D1372,Cadmium cyanide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29829,T3D1373,Zinc cadmium sulfide,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29830,T3D1373,Zinc cadmium sulfide,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29831,T3D1373,Zinc cadmium sulfide,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29832,T3D1373,Zinc cadmium sulfide,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29833,T3D1373,Zinc cadmium sulfide,Estrogen receptor,P03372,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29834,T3D1373,Zinc cadmium sulfide,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29835,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29836,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29837,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29838,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29839,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29840,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29841,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29842,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29843,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29844,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29845,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29846,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29847,T3D1373,Zinc cadmium sulfide,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29848,T3D1374,Cadmium(I) tetrachloroaluminate,C-jun-amino-terminal kinase-interacting protein 1,Q9UQF2,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29849,T3D1374,Cadmium(I) tetrachloroaluminate,C-jun-amino-terminal kinase-interacting protein 2,Q13387,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29850,T3D1374,Cadmium(I) tetrachloroaluminate,C-jun-amino-terminal kinase-interacting protein 3,Q9UPT6,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29851,T3D1374,Cadmium(I) tetrachloroaluminate,C-jun-amino-terminal kinase-interacting protein 4,O60271,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29852,T3D1374,Cadmium(I) tetrachloroaluminate,Estrogen receptor beta,Q92731,"Cadmium binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. (R059)"
29853,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 1,P28482,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29854,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 10,P53779,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29855,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 11,Q15759,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29856,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 12,P53778,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29857,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 13,O15264,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29858,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 14,Q16539,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29859,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 15,Q8TD08,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29860,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 3,P27361,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29861,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 4,P31152,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29862,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 6,Q16659,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29863,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 7,Q13164,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29864,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 8,P45983,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29865,T3D1374,Cadmium(I) tetrachloroaluminate,Mitogen-activated protein kinase 9,P45984,Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (R069)
29866,T3D1375,Beryllium silicate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29867,T3D1375,Beryllium silicate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29868,T3D1375,Beryllium silicate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29869,T3D1376,Zinc beryllium silicate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29870,T3D1376,Zinc beryllium silicate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29871,T3D1376,Zinc beryllium silicate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29872,T3D1377,Basic beryllium carbonate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29873,T3D1377,Basic beryllium carbonate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29874,T3D1377,Basic beryllium carbonate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29875,T3D1378,Beryllium carbonate tetrahydrate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29876,T3D1378,Beryllium carbonate tetrahydrate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29877,T3D1378,Beryllium carbonate tetrahydrate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29878,T3D1379,Beryllium sulfate tetrahydrate,"HLA class II histocompatibility antigen, DP alpha chain",P20036,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29879,T3D1379,Beryllium sulfate tetrahydrate,"HLA class II histocompatibility antigen, DP(W2) beta chain",P13763,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29880,T3D1379,Beryllium sulfate tetrahydrate,"HLA class II histocompatibility antigen, DP(W4) beta chain",P04440,"Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a major histocompatability (MHC) class II molecule. This MHC class II-beryllium-peptide complex is recognized by the T lymphocyte receptor, triggering CD4+ T lymphocyte activation and proliferation. The resulting inflammatory response is a cell-mediated process orchestrated by cytokines and results in the formation of (usually pulmonary) granulomas. (R079, R083)"
29881,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-1 subunit,Q06432,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29882,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-2 subunit,Q9Y698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29883,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-3 subunit,O60359,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29884,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-4 subunit,Q9UBN1,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29885,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-5 subunit,Q9UF02,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29886,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-6 subunit,Q9BXT2,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29887,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel gamma-7 subunit,P62955,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29888,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel subunit alpha-2/delta-1,P54289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29889,T3D0654,Cobalt(III) acetate,"Calcium channel, alpha 2/delta subunit 2",Q9NY47,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29890,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel subunit alpha-2/delta-3,Q8IZS8,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29891,T3D0654,Cobalt(III) acetate,Voltage-dependent calcium channel subunit alpha-2/delta-4,Q7Z3S7,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29892,T3D0654,Cobalt(III) acetate,Voltage-dependent L-type calcium channel subunit alpha-1F,O60840,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29893,T3D0654,Cobalt(III) acetate,Voltage-dependent L-type calcium channel subunit beta-3,P54284,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29894,T3D0654,Cobalt(III) acetate,Voltage-dependent L-type calcium channel subunit beta-4,O00305,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29895,T3D0654,Cobalt(III) acetate,Voltage-dependent N-type calcium channel subunit alpha-1B,Q00975,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29896,T3D0654,Cobalt(III) acetate,Voltage-dependent P/Q-type calcium channel subunit alpha-1A,O00555,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29897,T3D0654,Cobalt(III) acetate,Voltage-dependent R-type calcium channel subunit alpha-1E,Q15878,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29898,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-1 subunit,Q06432,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29899,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-2 subunit,Q9Y698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29900,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-3 subunit,O60359,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29901,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-4 subunit,Q9UBN1,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29902,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-5 subunit,Q9UF02,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29903,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-6 subunit,Q9BXT2,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29904,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel gamma-7 subunit,P62955,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29905,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel subunit alpha-2/delta-1,P54289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29906,T3D0655,Cobalt(II) carbonate,"Calcium channel, alpha 2/delta subunit 2",Q9NY47,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29907,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel subunit alpha-2/delta-3,Q8IZS8,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29908,T3D0655,Cobalt(II) carbonate,Voltage-dependent calcium channel subunit alpha-2/delta-4,Q7Z3S7,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29909,T3D0655,Cobalt(II) carbonate,Voltage-dependent L-type calcium channel subunit alpha-1F,O60840,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29910,T3D0655,Cobalt(II) carbonate,Voltage-dependent L-type calcium channel subunit beta-3,P54284,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29911,T3D0655,Cobalt(II) carbonate,Voltage-dependent L-type calcium channel subunit beta-4,O00305,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29912,T3D0655,Cobalt(II) carbonate,Voltage-dependent N-type calcium channel subunit alpha-1B,Q00975,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29913,T3D0655,Cobalt(II) carbonate,Voltage-dependent P/Q-type calcium channel subunit alpha-1A,O00555,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29914,T3D0655,Cobalt(II) carbonate,Voltage-dependent R-type calcium channel subunit alpha-1E,Q15878,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29915,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-1 subunit,Q06432,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29916,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-2 subunit,Q9Y698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29917,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-3 subunit,O60359,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29918,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-4 subunit,Q9UBN1,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29919,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-5 subunit,Q9UF02,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29920,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-6 subunit,Q9BXT2,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29921,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel gamma-7 subunit,P62955,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29922,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel subunit alpha-2/delta-1,P54289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29923,T3D0658,Cobalt(II) bromide,"Calcium channel, alpha 2/delta subunit 2",Q9NY47,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29924,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel subunit alpha-2/delta-3,Q8IZS8,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29925,T3D0658,Cobalt(II) bromide,Voltage-dependent calcium channel subunit alpha-2/delta-4,Q7Z3S7,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29926,T3D0658,Cobalt(II) bromide,Voltage-dependent L-type calcium channel subunit alpha-1F,O60840,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29927,T3D0658,Cobalt(II) bromide,Voltage-dependent L-type calcium channel subunit beta-3,P54284,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29928,T3D0658,Cobalt(II) bromide,Voltage-dependent L-type calcium channel subunit beta-4,O00305,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29929,T3D0658,Cobalt(II) bromide,Voltage-dependent N-type calcium channel subunit alpha-1B,Q00975,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29930,T3D0658,Cobalt(II) bromide,Voltage-dependent P/Q-type calcium channel subunit alpha-1A,O00555,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29931,T3D0658,Cobalt(II) bromide,Voltage-dependent R-type calcium channel subunit alpha-1E,Q15878,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29932,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-1 subunit,Q06432,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29933,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-2 subunit,Q9Y698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29934,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-3 subunit,O60359,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29935,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-4 subunit,Q9UBN1,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29936,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-5 subunit,Q9UF02,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29937,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-6 subunit,Q9BXT2,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29938,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel gamma-7 subunit,P62955,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29939,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel subunit alpha-2/delta-1,P54289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29940,T3D0659,Cobalt(II) chloride,"Calcium channel, alpha 2/delta subunit 2",Q9NY47,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29941,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel subunit alpha-2/delta-3,Q8IZS8,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29942,T3D0659,Cobalt(II) chloride,Voltage-dependent calcium channel subunit alpha-2/delta-4,Q7Z3S7,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29943,T3D0659,Cobalt(II) chloride,Voltage-dependent L-type calcium channel subunit alpha-1F,O60840,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29944,T3D0659,Cobalt(II) chloride,Voltage-dependent L-type calcium channel subunit beta-3,P54284,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29945,T3D0659,Cobalt(II) chloride,Voltage-dependent L-type calcium channel subunit beta-4,O00305,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29946,T3D0659,Cobalt(II) chloride,Voltage-dependent N-type calcium channel subunit alpha-1B,Q00975,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29947,T3D0659,Cobalt(II) chloride,Voltage-dependent P/Q-type calcium channel subunit alpha-1A,O00555,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29948,T3D0659,Cobalt(II) chloride,Voltage-dependent R-type calcium channel subunit alpha-1E,Q15878,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29949,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-1 subunit,Q06432,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29950,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-2 subunit,Q9Y698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29951,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-3 subunit,O60359,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29952,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-4 subunit,Q9UBN1,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29953,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-5 subunit,Q9UF02,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29954,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-6 subunit,Q9BXT2,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29955,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel gamma-7 subunit,P62955,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29956,T3D0660,Cobalt(II) fluoride,"Calcium channel, alpha 2/delta subunit 2",Q9NY47,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29957,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel subunit alpha-2/delta-3,Q8IZS8,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29958,T3D0660,Cobalt(II) fluoride,Voltage-dependent calcium channel subunit alpha-2/delta-4,Q7Z3S7,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29959,T3D0660,Cobalt(II) fluoride,Voltage-dependent L-type calcium channel subunit alpha-1F,O60840,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29960,T3D0660,Cobalt(II) fluoride,Voltage-dependent L-type calcium channel subunit beta-3,P54284,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29961,T3D0660,Cobalt(II) fluoride,Voltage-dependent L-type calcium channel subunit beta-4,O00305,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29962,T3D0660,Cobalt(II) fluoride,Voltage-dependent N-type calcium channel subunit alpha-1B,Q00975,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29963,T3D0660,Cobalt(II) fluoride,Voltage-dependent P/Q-type calcium channel subunit alpha-1A,O00555,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29964,T3D0660,Cobalt(II) fluoride,Voltage-dependent R-type calcium channel subunit alpha-1E,Q15878,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29965,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-1 subunit,Q06432,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29966,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-2 subunit,Q9Y698,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29967,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-3 subunit,O60359,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29968,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-4 subunit,Q9UBN1,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29969,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-5 subunit,Q9UF02,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29970,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-6 subunit,Q9BXT2,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29971,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel gamma-7 subunit,P62955,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29972,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel subunit alpha-2/delta-1,P54289,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29973,T3D0661,Cobalt(II) iodide,"Calcium channel, alpha 2/delta subunit 2",Q9NY47,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29974,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel subunit alpha-2/delta-3,Q8IZS8,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29975,T3D0661,Cobalt(II) iodide,Voltage-dependent calcium channel subunit alpha-2/delta-4,Q7Z3S7,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29976,T3D0661,Cobalt(II) iodide,Voltage-dependent L-type calcium channel subunit alpha-1F,O60840,"Cobalt blocks high-voltage-activated calcium channels, possibly impairing neurotransmission. (R253)"
29977,T3D0661,Cobalt(II) iodide,Voltage-dependent L-type calcium chan