CHEBI:34939 - prostaglandin D₃

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ChEBI Name prostaglandin D3 ChEBI ID CHEBI:34939 ChEBI ASCII Name prostaglandin D3 Definition A member of the class of prostaglandins D that is prosta-5,13,17-trien-1-oic acid substituted by hydroxy groups at positions 9 and 15 and an oxo group at position 11 (the 5Z,13E,15S,17Z-stereoisomer). Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C20H30O5 Net Charge 0 Average Mass 350.44920 Monoisotopic Mass 350.20932 InChI InChI=1S/C20H30O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h3-4,6-7,12-13,15-18,21-22H,2,5,8-11,14H2,1H3,(H,24,25)/b6-3-,7-4-,13-12+/t15-,16+,17+,18-/m0/s1 InChIKey ANOICLBSJIMQTA-WXGBOJPQSA-N SMILES CC\C=C/C[C@H](O)\C=C\[C@@H]1[C@@H](C\C=C/CCCC(O)=O)[C@@H](O)CC1=O Metabolite of Species Details Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Biological Role(s): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing prostaglandin D3 (CHEBI:34939) has role human metabolite (CHEBI:77746) prostaglandin D3 (CHEBI:34939) is a prostaglandins D (CHEBI:26337) prostaglandin D3 (CHEBI:34939) is conjugate acid of prostaglandin D3(1−) (CHEBI:132149) Incoming prostaglandin D3(1−) (CHEBI:132149) is conjugate base of prostaglandin D3 (CHEBI:34939) IUPAC Name (5Z,13E,15S,17Z)-9α,15-dihydroxy-11-oxoprosta-5,13,17-trien-1-oic acid Synonyms Sources (5Z)-7-[(1R,2R,5S)-5-hydroxy-2-[(1E,3S,5Z)-3-hydroxyocta-1,5-dien-1-yl]-3-oxocyclopentyl]hept-5-enoic acid HMDB (5Z,13E,15S,17Z)-9alpha,15-dihydroxy-11-oxoprosta-5,13,17-trien-1-oic acid HMDB 9S,15S-Dihydroxy-11-oxo-5Z,13E,17Z-prostatrienoic acid HMDB Prostaglandin D3 KEGG COMPOUND Manual Xrefs Databases C13802 KEGG COMPOUND HMDB0003034 HMDB LMFA03010142 LIPID MAPS View more database links Registry Numbers Types Sources 5995201 Reaxys Registry Number Reaxys 71902-47-1 CAS Registry Number ChemIDplus Citations Types Sources 230492 PubMed citation Europe PMC 23595524 PubMed citation Europe PMC 23833568 PubMed citation Europe PMC Last Modified 21 July 2016