<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4569</id>
  <title>T3D4515</title>
  <common-name>Hexythiazox</common-name>
  <description>Hexythiazox is an acaricide used for the control of eggs and larvae of many phytophagous mites and functions as a mite growth regulator. It is also considered as a thiazolidine based acaricide that has long-lasting effects against many kinds of mites and is applied at any stage of the plant growth from budding to fruiting. Its mode of action is non-systemic with contact and stomach action.</description>
  <cas>78587-05-0</cas>
  <pubchem-id>13218777</pubchem-id>
  <chemical-formula>C17H21ClN2O2S</chemical-formula>
  <weight nil="true"/>
  <appearance>White powder.</appearance>
  <melting-point></melting-point>
  <boiling-point></boiling-point>
  <density nil="true"/>
  <solubility></solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure></route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity></mechanism-of-toxicity>
  <metabolism></metabolism>
  <toxicity>Oral LD50 (rat) &gt; 5000 mg/kg bw
Dermal LD50 (rat) &gt; 5000 mg/kg bw
Inhalation &gt; 2.0 mg/l/4 h (whole body exposure)</toxicity>
  <lethaldose></lethaldose>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>This is a man-made compound that is used as a pesticide.</use-source>
  <min-risk-level></min-risk-level>
  <health-effects>Hexythiazox increased incidences of tumours in rodents exposed to hexythiazox and doesn't present a carcinogenic risk to humans at exposure  levels associated with residues in food. (L2110)</health-effects>
  <symptoms></symptoms>
  <treatment></treatment>
  <created-at type="dateTime">2014-08-29T06:51:44Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:26:52Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia></wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id>C18467</kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id>CHEBI:39328</chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id></ctd-id>
  <stitch-id></stitch-id>
  <drugbank-id></drugbank-id>
  <pdb-id></pdb-id>
  <actor-id></actor-id>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>[H][C@@]1(C)N(C(O)=NC2CCCCC2)C(=O)S[C@@]1([H])C1=CC=C(Cl)C=C1</moldb-smiles>
  <moldb-formula>C17H21ClN2O2S</moldb-formula>
  <moldb-inchi>InChI=1S/C17H21ClN2O2S/c1-11-15(12-7-9-13(18)10-8-12)23-17(22)20(11)16(21)19-14-5-3-2-4-6-14/h7-11,14-15H,2-6H2,1H3,(H,19,21)/t11-,15+/m0/s1</moldb-inchi>
  <moldb-inchikey>InChIKey=XGWIJUOSCAQSSV-XHDPSFHLSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">352.879</moldb-average-mass>
  <moldb-mono-mass type="decimal">352.101226323</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp></logp>
  <hmdb-id></hmdb-id>
  <chembl-id>CHEMBL1904578</chembl-id>
  <chemspider-id>10469179</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference></synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
