CHEBI:138332 - 11(S)-HETE

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ChEBI Name 11(S)-HETE ChEBI ID CHEBI:138332 ChEBI ASCII Name 11(S)-HETE Definition An 11-HETE in which the chiral centre at position 11 has S-configuration. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C20H32O3 Net Charge 0 Average Mass 320.467 Monoisotopic Mass 320.23514 InChI InChI=1S/C20H32O3/c1-2-3-4-5-7-10-13-16-19(21)17-14-11-8-6-9-12-15-18-20(22)23/h6-7,9-11,13-14,16,19,21H,2-5,8,12,15,17-18H2,1H3,(H,22,23)/b9-6-,10-7-,14-11-,16-13+/t19-/m1/s1 InChIKey GCZRCCHPLVMMJE-YZGNWCGPSA-N SMILES C(CCC/C=C\C/C=C\C[C@@H](/C=C/C=C\CCCCC)O)(=O)O Metabolite of Species Details Mus musculus (NCBI:txid10090) 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 11-HETE ) View more via ChEBI Ontology ChEBI Ontology Outgoing 11(S)-HETE (CHEBI:138332) has role mouse metabolite (CHEBI:75771) 11(S)-HETE (CHEBI:138332) is a 11-HETE (CHEBI:72606) 11(S)-HETE (CHEBI:138332) is conjugate acid of 11(S)-HETE(1−) (CHEBI:137567) 11(S)-HETE (CHEBI:138332) is enantiomer of 11(R)-HETE (CHEBI:34126) Incoming 11(S)-HETE(1−) (CHEBI:137567) is conjugate base of 11(S)-HETE (CHEBI:138332) 11(R)-HETE (CHEBI:34126) is enantiomer of 11(S)-HETE (CHEBI:138332) IUPAC Name (5Z,8Z,11S,12E,14Z)-11-hydroxyicosa-5,8,12,14-tetraenoic acid Synonyms Sources (11S)-HETE ChEBI (5Z,8Z,11S,12E,14Z)-11-hydroxyeicosatetraenoic acid ChEBI (5Z,8Z,11S,12E,14Z)-11-hydroxyicosatetraenoic acid ChEBI 11(S)-hydroxy-(5Z,8Z,12E,14Z)-eicosatetraenoic acid ChEBI 11(S)-hydroxy-(5Z,8Z,12E,14Z)-icosatetraenoic acid ChEBI 11S-HETE LIPID MAPS 11S-hydroxy-5Z,8Z,11E,14Z-eicosatetraenoic acid LIPID MAPS Manual Xref Database LMFA03060003 LIPID MAPS View more database links Registry Number Type Source 7588271 Reaxys Registry Number Reaxys Citations Types Sources 7961871 PubMed citation Europe PMC 9822682 PubMed citation Europe PMC Last Modified 30 August 2017