CHEBI:73944 - 2,3-dinor-6-oxoprostaglandin F1α

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ChEBI Name 2,3-dinor-6-oxoprostaglandin F1α
ChEBI ID CHEBI:73944
ChEBI ASCII Name 2,3-dinor-6-oxoprostaglandin F1alpha
Definition A prostanoid that is prostaglandin F1α lacking two methylenes in the carboxyalkyl chain and bearing an oxo group at the 6-position.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C18H30O6
Net Charge 0
Average Mass 342.42720
Monoisotopic Mass 342.20424
InChI InChI=1S/C18H30O6/c1-2-3-4-5-12(19)6-8-14-15(17(22)11-16(14)21)10-13(20)7-9-18(23)24/h6,8,12,14-17,19,21-22H,2-5,7,9-11H2,1H3,(H,23,24)/b8-6+/t12-,14+,15+,16+,17-/m0/s1
InChIKey DNKGWNLXBRCUCF-NLOSNHEGSA-N
SMILES CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1CC(=O)CCC(O)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2,3-dinor-6-oxoprostaglandin F1α (CHEBI:73944) has functional parent prostaglandin F1α (CHEBI:28852)
2,3-dinor-6-oxoprostaglandin F1α (CHEBI:73944) has role metabolite (CHEBI:25212)
2,3-dinor-6-oxoprostaglandin F1α (CHEBI:73944) is a 4-oxo monocarboxylic acid (CHEBI:35950)
2,3-dinor-6-oxoprostaglandin F1α (CHEBI:73944) is a prostanoid (CHEBI:26347)
2,3-dinor-6-oxoprostaglandin F1α (CHEBI:73944) is a secondary alcohol (CHEBI:35681)
Incoming 19-hydroxy-2,3-dinor-6-oxoprostaglandin F1α (CHEBI:73951) has functional parent 2,3-dinor-6-oxoprostaglandin F1α (CHEBI:73944)
IUPAC Names
(13E,15S)-9α,11α,15-trihydroxy-2,3-dinor-6-oxoprost-13-en-1-oic acid
5-{(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]cyclopentyl}-4-oxopentanoic acid
Synonyms Sources
2,3-dinor, 6-keto-PGF1α LIPID MAPS
2,3-dinor-6-keto-pgf1α ChemIDplus
2,3-dinor-6-keto-PGF1α ChEBI
2,3-dinor-6-ketoprostaglandin F1α ChemIDplus
2,3-dinor-6-oxo-pgf1α ChemIDplus
2,3-dinor-6-oxo-PGF1α ChEBI
2,3-dinor-6-oxo-prostaglandin F1α ChEBI
2,3-dkpgf1α ChemIDplus
Pgi2-M ChemIDplus
Manual Xrefs Databases
HMDB0002277 HMDB
LMFA03010089 LIPID MAPS
View more database links
Registry Numbers Types Sources
4540372 Reaxys Registry Number Reaxys
64700-71-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10941682 PubMed citation Europe PMC
22311294 PubMed citation Europe PMC
8150859 PubMed citation Europe PMC
Last Modified
23 October 2015