CHEBI:15558 - 15(S)-HETE

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 15(S)-HETE
ChEBI ID CHEBI:15558
ChEBI ASCII Name 15(S)-HETE
Definition An optically active form of 15-HETE having 15(S)-configuration..
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:18507, CHEBI:10824, CHEBI:147
Supplier Information
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Formula C20H32O3
Net Charge 0
Average Mass 320.46628
InChI InChI=1S/C20H32O3/c1-2-3-13-16-19(21)17-14-11-9-7-5-4-6-8-10-12-15-18-20(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 JSFATNQSLKRBCI-VAEKSGALSA-N
SMILES CCCCC[C@H](O)\C=C\C=C/C\C=C/C\C=C/CCCC(O)=O
Metabolite of Species Details
Mus musculus (NCBI:10090) Source: BioModels - MODEL1507180067 See: PubMed
Homo sapiens (NCBI:9606) 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): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via (5Z,8Z,11Z,13E)-15-HETE )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 15(S)-HETE (CHEBI:15558) has role human metabolite (CHEBI:77746)
15(S)-HETE (CHEBI:15558) has role mouse metabolite (CHEBI:75771)
15(S)-HETE (CHEBI:15558) is a (5Z,8Z,11Z,13E)-15-HETE (CHEBI:64017)
15(S)-HETE (CHEBI:15558) is conjugate acid of 15(S)-HETE(1−) (CHEBI:57409)
15(S)-HETE (CHEBI:15558) is enantiomer of 15(R)-HETE (CHEBI:63989)
Incoming 15(S)-HETE(1−) (CHEBI:57409) is conjugate base of 15(S)-HETE (CHEBI:15558)
15(R)-HETE (CHEBI:63989) is enantiomer of 15(S)-HETE (CHEBI:15558)
IUPAC Name
(5Z,8Z,11Z,13E,15S)-15-hydroxyicosa-5,8,11,13-tetraenoic acid
INN Source
icomucret ChemIDplus
Synonyms Sources
(15S)-15-Hydroxy-5,8,11-cis-13-trans-eicosatetraenoate KEGG COMPOUND
(15S)-15-hydroxy-5,8,11-cis-13-trans-eicosatetraenoate ChEBI
(15S)-15-Hydroxy-5,8,11-cis-13-trans-icosatetraenoate KEGG COMPOUND
(15S)-15-hydroxy-5,8,11-cis-13-trans-icosatetraenoate ChEBI
(15S)-hydroxy-(5Z,8Z,11Z,13E)-eicosatetraenoic acid ChEBI
(15S)-hydroxyeicosa-(5Z,8Z,11Z,13E)-tetraenoic acid ChEBI
(5Z,8Z,11Z,13E)-(15S)-15-Hydroxyicosa-5,8,11,13-tetraenoic acid KEGG COMPOUND
(5Z,8Z,11Z,13E,15S)-15-hydroxy-5,8,11,13-eicosatetraenoic acid ChEBI
(5Z,8Z,11Z,13E,15S)-15-hydroxyeicosa-5,8,11,13-tetraenoic acid ChEBI
15(S)-HETE KEGG COMPOUND
15(S)-hydroxyeicosatetraenoic acid ChEBI
15S-HETE LIPID MAPS
Database Links Databases
C04742 KEGG COMPOUND
D08931 KEGG DRUG
HMDB03876 HMDB
LMFA03060001 LIPID MAPS
View more database links
Registry Numbers Types Sources
2470466 Beilstein Registry Number Beilstein
54845-95-3 CAS Registry Number KEGG COMPOUND
54845-95-3 CAS Registry Number ChemIDplus
6125815 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11212240 PubMed citation CiteXplore
15613483 PubMed citation CiteXplore
15964853 PubMed citation CiteXplore
18494609 PubMed citation CiteXplore
22068350 PubMed citation CiteXplore
Last Modified
27 January 2016