CHEBI:138110 - 16(S)-HETE

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ChEBI Name 16(S)-HETE
ChEBI ID CHEBI:138110
ChEBI ASCII Name 16(S)-HETE
Definition A 16-HETE in which the chiral centre at position 16 has S-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/c1-2-3-16-19(21)17-14-12-10-8-6-4-5-7-9-11-13-15-18-20(22)23/h4-5,8-11,14,17,19,21H,2-3,6-7,12-13,15-16,18H2,1H3,(H,22,23)/b5-4-,10-8-,11-9-,17-14-/t19-/m0/s1
InChIKey JEKNPVYFNMZRJG-IFOZKBMWSA-N
SMILES O=C(CCC/C=C\C/C=C\C/C=C\C/C=C\[C@H](CCCC)O)O
Metabolite of Species Details
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.
Application(s): anti-inflammatory agent
Any compound that has anti-inflammatory effects.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 16(S)-HETE (CHEBI:138110) has role anti-inflammatory agent (CHEBI:67079)
16(S)-HETE (CHEBI:138110) has role human xenobiotic metabolite (CHEBI:76967)
16(S)-HETE (CHEBI:138110) is a 16-HETE (CHEBI:63994)
16(S)-HETE (CHEBI:138110) is conjugate acid of 16(S)-HETE(1−) (CHEBI:137167)
16(S)-HETE (CHEBI:138110) is enantiomer of 16(R)-HETE (CHEBI:34162)
Incoming 16(S)-HETE(1−) (CHEBI:137167) is conjugate base of 16(S)-HETE (CHEBI:138110)
16(R)-HETE (CHEBI:34162) is enantiomer of 16(S)-HETE (CHEBI:138110)
IUPAC Name
(5Z,8Z,11Z,14Z,16S)-16-hydroxyicosa-5,8,11,14-tetraenoic acid
Synonyms Sources
(16S)-HETE ChEBI
(16S)-hydroxyarachidonic acid ChEBI
(5Z,8Z,11Z,14Z,16S)-16-hydroxyeicosa-5,8,11,14-tetraenoic acid ChEBI
(5Z,8Z,11Z,14Z,16S)-16-hydroxyeicosatetraenoic acid ChEBI
(5Z,8Z,11Z,14Z,16S)-16-hydroxyicosatetraenoic acid ChEBI
16(S)-hydroxy-(5Z,8Z,11Z,14Z)-eicosatetraenoic acid ChEBI
16(S)-hydroxy-(5Z,8Z,11Z,14Z)-icosatetraenoic acid ChEBI
Registry Number Type Source
9287648 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
10908295 PubMed citation Europe PMC
14552765 PubMed citation Europe PMC
28655971 PubMed citation Europe PMC
Last Modified
09 August 2017