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CHEBI:134510 - prostaglandin A3

ChEBI IDCHEBI:134510
ChEBI Nameprostaglandin A3
Stars
ASCII Nameprostaglandin A3
DefinitionA member of the class of prostaglandins A that is prosta-5,10,13,17-tetraen-1-oic acid carrying oxo and hydroxy substituents at positions 9 and 15 respectively (the 5Z,13E,15S,17Z-stereoisomer).
Last Modified27 February 2018
SubmitterSteve
DownloadsMolfile
FormulaC20H28O4
Net Charge0
Average Mass332.440
Monoisotopic Mass332.19876
SMILESCC/C=C\C[C@H](O)/C=C/[C@H]1C=CC(=O)[C@@H]1C/C=C\CCCC(=O)O
InChIInChI=1S/C20H28O4/c1-2-3-6-9-17(21)14-12-16-13-15-19(22)18(16)10-7-4-5-8-11-20(23)24/h3-4,6-7,12-18,21H,2,5,8-11H2,1H3,(H,23,24)/b6-3-,7-4-,14-12+/t16-,17-,18+/m0/s1
InChIKeyKSIRMUMXJFWKAC-FHJHOUOTSA-N
Species of MetaboliteComponentSourceComments
Canis lupus familiaris (ncbitaxon:9615) - PubMed (10410384)
Roles Classification
Biological Role:
mammalian metabolite  Any animal metabolite produced during a metabolic reaction in mammals.
ChEBI Ontology
Outgoing Relation(s)
prostaglandin A3 (CHEBI:134510) has role mammalian metabolite (CHEBI:75768)
prostaglandin A3 (CHEBI:134510) is a prostaglandins A (CHEBI:26334)
prostaglandin A3 (CHEBI:134510) is a secondary allylic alcohol (CHEBI:134396)
prostaglandin A3 (CHEBI:134510) is conjugate acid of prostaglandin A3(1−) (CHEBI:133423)
Incoming Relation(s)
prostaglandin A3(1−) (CHEBI:133423) is conjugate base of prostaglandin A3 (CHEBI:134510)
IUPAC Name 
(5Z,13E,15S,17Z)-15-hydroxy-9-oxoprosta-5,10,13,17-tetraen-1-oic acid
Synonym  Source
PGA3ChEBI
Registry NumbersSources
Reaxys:8937043Reaxys
Citations