<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4492</id>
  <title>T3D4438</title>
  <common-name>Coproporphyrinogen III</common-name>
  <description>Coproporphyrinogen III oxidase is deficient in hereditary coproporphyria. These persons usually have enhanced excretion even in a subclinical state of the disease.  (A3500).</description>
  <cas>2624-63-7</cas>
  <pubchem-id>321</pubchem-id>
  <chemical-formula>C36H44N4O8</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 nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>This is an endogenously produced metabolite found in the human body. It is used in metabolic reactions, catabolic reactions or waste generation.</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2014-08-29T06:51:16Z</created-at>
  <updated-at type="dateTime">2026-04-05T11:56:31Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Coproporphyrinogen III</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C03263</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>15439</chebi-id>
  <biocyc-id>COPROPORPHYRINOGEN_III</biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB04461</drugbank-id>
  <pdb-id>CP3</pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CC1=C2CC3=C(C)C(CCC(O)=O)=C(CC4=C(CCC(O)=O)C(C)=C(CC5=C(CCC(O)=O)C(C)=C(CC(N2)=C1CCC(O)=O)N5)N4)N3</moldb-smiles>
  <moldb-formula>C36H44N4O8</moldb-formula>
  <moldb-inchi>InChI=1S/C36H44N4O8/c1-17-21(5-9-33(41)42)29-14-27-19(3)22(6-10-34(43)44)30(39-27)15-28-20(4)24(8-12-36(47)48)32(40-28)16-31-23(7-11-35(45)46)18(2)26(38-31)13-25(17)37-29/h37-40H,5-16H2,1-4H3,(H,41,42)(H,43,44)(H,45,46)(H,47,48)</moldb-inchi>
  <moldb-inchikey>NIUVHXTXUXOFEB-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">660.7566</moldb-average-mass>
  <moldb-mono-mass type="decimal">660.315914404</moldb-mono-mass>
  <origin>Endogenous</origin>
  <state>Solid</state>
  <logp nil="true"/>
  <hmdb-id>HMDB01261</hmdb-id>
  <chembl-id>CHEMBL1231891</chembl-id>
  <chemspider-id>315</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;Ichiro Kojima, Kenji Maruhashi, Yasuo Fujiwara, &amp;#8220;Process for producing coproporphyrin &lt;span class="caps"&gt;III&lt;/span&gt;.&amp;#8221; U.S. Patent US4334021, issued September, 1978.&lt;/p&gt;</synthesis-reference>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003398</chemdb-id>
  <dsstox-id>DTXSID40180875</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>3-[9,14,20-tris(2-carboxyethyl)-5,10,15,19-tetramethyl-21,22,23,24-tetraazapentacyclo[16.2.1.1^{3,6}.1^{8,11}.1^{13,16}]tetracosa-1(20),3,5,8,10,13,15,18-octaen-4-yl]propanoic acid</iupac>
</compound>
