<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4830</id>
  <title>T3D4775</title>
  <common-name>Fenofibrate</common-name>
  <description>An antilipemic agent which reduces both cholesterol and triglycerides in the blood. </description>
  <cas>49562-28-9</cas>
  <pubchem-id>3339</pubchem-id>
  <chemical-formula>C20H21ClO4</chemical-formula>
  <weight nil="true"/>
  <appearance>White powder.</appearance>
  <melting-point>80.5°C</melting-point>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility>0.25mg/ml at 25°C</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure>Fenofibrate is well absorbed from the gastrointestinal tract. After absorption, fenofibrate is mainly excreted in the urine in the form of metabolites, primarily fenofibric acid and fenofibric acid glucuronide</route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity>Fenofibrate exerts its therapeutic effects through activation of peroxisome proliferator activated receptor a (PPARa). This increases lipolysis and elimination of triglyceride-rich particles from plasma by activating lipoprotein lipase and reducing production of apoprotein C-III. The resulting fall in triglycerides produces an alteration in the size and composition of LDL from small, dense particles, to large buoyant particles. These larger particles have a greater affinity for cholesterol receptors and are catabolized rapidly.</mechanism-of-toxicity>
  <metabolism>Route of Elimination: Fenofibric acid is primarily conjugated with glucuronic acid and then excreted in urine. Following oral administration in healthy volunteers, approximately 60% of a single dose of radiolabelled fenofibrate appeared in urine, primarily as fenofibric acid and its glucuronate conjugate and 25% was excreted in the feces.Half Life: 20 hours</metabolism>
  <toxicity>LD&lt;sub&gt;50&lt;/sub&gt;=1600 mg/kg (Oral, in mice)</toxicity>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>For use as adjunctive therapy to diet to reduce elevated LDL-C, Total-C,Triglycerides and Apo B, and to increase HDL-C in adult patients with primary hypercholesterolemia or mixed dyslipidemia (Fredrickson Types IIa and IIb)</use-source>
  <min-risk-level nil="true"/>
  <health-effects>Investigated as a teratogen and reproductive hazard.</health-effects>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2014-09-11T05:16:04Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:26:57Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Fenofibrate</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C07586</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>5001</chebi-id>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB01039</drugbank-id>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CC(C)OC(=O)C(C)(C)OC1=CC=C(C=C1)C(=O)C1=CC=C(Cl)C=C1</moldb-smiles>
  <moldb-formula>C20H21ClO4</moldb-formula>
  <moldb-inchi>InChI=1S/C20H21ClO4/c1-13(2)24-19(23)20(3,4)25-17-11-7-15(8-12-17)18(22)14-5-9-16(21)10-6-14/h5-13H,1-4H3</moldb-inchi>
  <moldb-inchikey>InChIKey=YMTINGFKWWXKFG-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">360.831</moldb-average-mass>
  <moldb-mono-mass type="decimal">360.112836867</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp>5.3</logp>
  <hmdb-id>HMDB15173</hmdb-id>
  <chembl-id>CHEMBL672</chembl-id>
  <chemspider-id>3222</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>&lt;p&gt;Jean-Francois Boyer, &amp;#8220;Medicine based on fenofibrate, and a method of preparing it.&amp;#8221; U.S. Patent US4800079, issued January, 1988.&lt;/p&gt;</synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
