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

ChEBI IDCHEBI:137746
ChEBI Name(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid
Stars
ASCII Name(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosatetraenoic acid
DefinitionAn icosanoid that is (6E,8Z,11Z,13E)-icosatetraenoic acid substituted at positions 5 and 15 by oxo and hydroxy groups respectively.
Last Modified5 March 2018
SubmitterSteve
DownloadsMolfile
FormulaC20H30O4
Net Charge0
Average Mass334.456
Monoisotopic Mass334.21441
SMILESCCCCC[C@H](O)/C=C/C=C\C/C=C\C=C\C(=O)CCCC(=O)O
InChIInChI=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
InChIKeyRIUDRKHGFDAKPO-WWWYWCMOSA-N
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
human xenobiotic metabolite  Any human metabolite produced by metabolism of a xenobiotic compound in humans.
ChEBI Ontology
Outgoing Relation(s)
(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)
IUPAC Name 
(6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosa-6,8,11,13-tetraenoic acid
Synonyms  Source
5-oxo-15-HETEChEBI
5-Oxo-15-hydroxy-6,8,11,13-eicosatetraenoic acidChemIDplus
Registry NumbersSources
Reaxys:21359907Reaxys
CAS:142828-12-4ChemIDplus
Citations