CHEBI:88346 - 13,14-dihydroprostaglandin F2α

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ChEBI Name 13,14-dihydroprostaglandin F2α
ChEBI ID CHEBI:88346
ChEBI ASCII Name 13,14-dihydroprostaglandin F2alpha
Definition A prostaglandins Fα that is prost-5-en-1-oic acid substituted by hydroxy groups at positions 9, 11 and 15.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C20H36O5
Net Charge 0
Average Mass 356.498
Monoisotopic Mass 356.25627
InChI InChI=1S/C20H36O5/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/h4,7,15-19,21-23H,2-3,5-6,8-14H2,1H3,(H,24,25)/b7-4-/t15-,16+,17+,18-,19+/m0/s1
InChIKey LLQBSJQTCKVWTD-NFUXFLSFSA-N
SMILES [C@@H]1(CC[C@@H](O)CCCCC)[C@H]([C@H](C[C@H]1O)O)C/C=C\CCCC(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: MetaboLights Study
Rattus norvegicus (NCBI:txid10116) See: PubMed
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): rat metabolite
Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 13,14-dihydroprostaglandin F2α (CHEBI:88346) has functional parent prostaglandin F2α (CHEBI:15553)
13,14-dihydroprostaglandin F2α (CHEBI:88346) has role rat metabolite (CHEBI:86264)
13,14-dihydroprostaglandin F2α (CHEBI:88346) is a hydroxy monocarboxylic acid (CHEBI:35868)
13,14-dihydroprostaglandin F2α (CHEBI:88346) is a prostaglandins Fα (CHEBI:36066)
13,14-dihydroprostaglandin F2α (CHEBI:88346) is conjugate acid of 13,14-dihydroprostaglandin F2α(1−) (CHEBI:133376)
Incoming 13,14-dihydroprostaglandin F2α(1−) (CHEBI:133376) is conjugate base of 13,14-dihydroprostaglandin F2α (CHEBI:88346)
IUPAC Name
(5Z,9α,11α,15S)-9,11,15-trihydroxyprost-5-en-1-oic acid
Synonyms Sources
13,14-dihydro-PGF2α ChEBI
13,14-dihydro-prostaglandin F2α LIPID MAPS
13,14-Dihydrodinoprost HMDB
13,14-Dihydroprostaglandin F2-alpha ChemIDplus
9S,11R,15S-trihydroxy-5Z-prostenoic acid LIPID MAPS
Manual Xrefs Databases
HMDB0004239 HMDB
LMFA03010079 LIPID MAPS
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Registry Numbers Types Sources
27376-74-5 CAS Registry Number ChemIDplus
2885169 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
3365066 PubMed citation Europe PMC
6572072 PubMed citation Europe PMC
9690712 PubMed citation Europe PMC
Last Modified
09 February 2017