CHEBI:137746 - (6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid

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ChEBI Name (6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid
ChEBI ASCII Name (6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid
Definition An icosanoid that is (6E,8Z,11Z,13E)-icosatetraenoic acid substituted at positions 5 and 15 by oxo and hydroxy groups respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C20H30O4
Net Charge 0
Average Mass 334.451
Monoisotopic Mass 334.214
InChI InChI=1S/C20H30O4/c1-2-3-9-13-18(21)14-10-7-5-4-6-8-11-15-19(22)16-12-17-20(23)24/h5-8,10-11,14-15,18,21H,2-4,9,12-13,16-17H2,1H3,(H,23,24)/b7-5-,8-6-,14-10+,15-11+/t18-/m0/s1
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.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid (CHEBI:137746) has role human xenobiotic metabolite (CHEBI:76967)
(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid (CHEBI:137746) is a enone (CHEBI:51689)
(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid (CHEBI:137746) is a hydroxy polyunsaturated fatty acid (CHEBI:140345)
(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid (CHEBI:137746) is a icosanoid (CHEBI:23899)
(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid (CHEBI:137746) is a long-chain fatty acid (CHEBI:15904)
(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid (CHEBI:137746) is a oxo fatty acid (CHEBI:59644)
(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid (CHEBI:137746) is a secondary allylic alcohol (CHEBI:134396)
(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosa-6,8,11,13-tetraenoic acid
Synonyms Sources
5-oxo-15-HETE ChEBI
5-Oxo-15-hydroxy-6,8,11,13-eicosatetraenoic acid ChemIDplus
Registry Numbers Types Sources
142828-12-4 CAS Registry Number ChemIDplus
21359907 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1326548 PubMed citation Europe PMC
1618754 PubMed citation Europe PMC
7706749 PubMed citation Europe PMC
7797484 PubMed citation Europe PMC
Last Modified
05 March 2018