CHEBI:132303 - (8R,9S)-EET

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ChEBI Name (8R,9S)-EET
ChEBI ID CHEBI:132303
ChEBI ASCII Name (8R,9S)-EET
Definition An 8,9-EET in which the epoxy moiety has 8R,9S-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C20H32O3
Net Charge 0
Average Mass 320.467
Monoisotopic Mass 320.23514
InChI InChI=1S/C20H32O3/c1-2-3-4-5-6-7-8-9-12-15-18-19(23-18)16-13-10-11-14-17-20(21)22/h6-7,9-10,12-13,18-19H,2-5,8,11,14-17H2,1H3,(H,21,22)/b7-6-,12-9-,13-10-/t18-,19+/m0/s1
InChIKey DBWQSCSXHFNTMO-QJVNBQAESA-N
SMILES C(CCC)C/C=C\C/C=C\C[C@H]1[C@@H](C/C=C\CCCC(O)=O)O1
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: PubMed
Rattus norvegicus (NCBI:txid10116) See: PubMed
Stenotomus chrysops (NCBI:txid35579) See: PubMed
Homo sapiens (NCBI:txid9606) 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): human xenobiotic metabolite
Any human metabolite produced by metabolism of a xenobiotic compound in humans.
marine xenobiotic metabolite
Any metabolite produced by metabolism of a xenobiotic compound in marine macro- and microorganisms.
rat metabolite
Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via 8,9-EET )
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via EET )
Application(s): platelet aggregation inhibitor
A drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
(via EET )
anti-inflammatory drug
A substance that reduces or suppresses inflammation.
(via EET )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (8R,9S)-EET (CHEBI:132303) has role human xenobiotic metabolite (CHEBI:76967)
(8R,9S)-EET (CHEBI:132303) has role marine xenobiotic metabolite (CHEBI:83399)
(8R,9S)-EET (CHEBI:132303) has role mouse metabolite (CHEBI:75771)
(8R,9S)-EET (CHEBI:132303) has role rat metabolite (CHEBI:86264)
(8R,9S)-EET (CHEBI:132303) is a 8,9-EET (CHEBI:34490)
(8R,9S)-EET (CHEBI:132303) is conjugate acid of (8R,9S)-EET(1−) (CHEBI:131975)
(8R,9S)-EET (CHEBI:132303) is enantiomer of (8S,9R)-EET (CHEBI:132302)
Incoming (8R,9S)-EET(1−) (CHEBI:131975) is conjugate base of (8R,9S)-EET (CHEBI:132303)
(8S,9R)-EET (CHEBI:132302) is enantiomer of (8R,9S)-EET (CHEBI:132303)
IUPAC Name
(5Z)-7-{(2R,3S)-3-[(2Z,5Z)-undeca-2,5-dien-1-yl]oxiran-2-yl}hept-5-enoic acid
Synonyms Sources
(8R,9S)-EpETrE ChEBI
(8R,9S)-epoxy-(5Z,11Z,14Z)-eicosatrienoic acid ChEBI
(8R,9S)-epoxy-(5Z,11Z,14Z)-icosatrienoic acid ChEBI
8(R),9(S)-EET ChEBI
8R,9S-EET LIPID MAPS
8R,9S-EpETrE LIPID MAPS
8R,9S-epoxy-5Z,11Z,14Z-eicosatrienoic acid LIPID MAPS
Manual Xref Database
LMFA03080018 LIPID MAPS
View more database links
Registry Number Type Source
4697203 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
15084647 PubMed citation Europe PMC
20972997 PubMed citation Europe PMC
22628547 PubMed citation Europe PMC
7840649 PubMed citation Europe PMC
9606961 PubMed citation Europe PMC
Last Modified
28 June 2016