CHEBI:15558 - 15(S)-HETE

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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 eMolecules:1934471, ZINC000004629861 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 320.46628 Monoisotopic Mass 320.23514 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:txid10090) Source: BioModels - MODEL1507180067 See: PubMed 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): 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 Manual Xrefs Databases C04742 KEGG COMPOUND D08931 KEGG DRUG HMDB0003876 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 Last Modified 27 January 2016