CHEBI:91286 - 5(S),15(S)-DiHETE

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ChEBI Name 5(S),15(S)-DiHETE ChEBI ID CHEBI:91286 ChEBI ASCII Name 5(S),15(S)-DiHETE Definition A DiHETE that is (6E,8Z,11Z,13E)-icosatetraenoic acid in which the two hydroxy substituents are placed at the 5S- and 15S-positions. 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 C20H32O4 Net Charge 0 Average Mass 336.466 Monoisotopic Mass 336.23006 InChI InChI=1S/C20H32O4/c1-2-3-9-13-18(21)14-10-7-5-4-6-8-11-15-19(22)16-12-17-20(23)24/h5-8,10-11,14-15,18-19,21-22H,2-4,9,12-13,16-17H2,1H3,(H,23,24)/b7-5-,8-6-,14-10+,15-11+/t18-,19+/m0/s1 InChIKey UXGXCGPWGSUMNI-BVHTXILBSA-N SMILES C(CCC[C@@H](/C=C/C=C\C/C=C\C=C\[C@H](CCCCC)O)O)(O)=O Metabolite of Species Details Rattus norvegicus (NCBI:txid10116) 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): rat metabolite Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus). human xenobiotic metabolite Any human metabolite produced by metabolism of a xenobiotic compound in humans. View more via ChEBI Ontology ChEBI Ontology Outgoing 5(S),15(S)-DiHETE (CHEBI:91286) has role human xenobiotic metabolite (CHEBI:76967) 5(S),15(S)-DiHETE (CHEBI:91286) has role rat metabolite (CHEBI:86264) 5(S),15(S)-DiHETE (CHEBI:91286) is a dihydroxyicosatetraenoic acid (CHEBI:72868) 5(S),15(S)-DiHETE (CHEBI:91286) is conjugate acid of 5(S),15(S)-DiHETE(1−) (CHEBI:90813) Incoming 5(S),15(S)-DiHETE(1−) (CHEBI:90813) is conjugate base of 5(S),15(S)-DiHETE (CHEBI:91286) IUPAC Name (5S,6E,8Z,11Z,13E,15S)-5,15-dihydroxyicosa-6,8,11,13-tetraenoic acid Synonyms Sources (5S,15S)-dihydroxy-(6E,8Z,11Z,13E)-eicosatetraenoic acid ChEBI (5S,15S)-dihydroxy-(6E,8Z,11Z,13E)-icosatetraenoic acid ChEBI (5S,6E,8Z,11Z,13E,15S)-5,15-dihydroxyicosatetraenoic acid ChEBI 5(S),15(S)-Dihydroxy-6,13-trans-8,11-cis-eicosatetraenoic acid ChemIDplus 5,15-DiHETE HMDB 5,15-Dihydroxy-6,8,11,13-eicosatetraenoic acid HMDB 5,15-Dihydroxyeicosatetraenoic acid HMDB 5S,15S-DiHETE LIPID MAPS 5S,15S-dihydroxy-6E,8Z,11Z,13E-eicosatetraenoic acid LIPID MAPS Manual Xrefs Databases HMDB0010216 HMDB LMFA03060010 LIPID MAPS View more database links Registry Numbers Types Sources 4472597 Reaxys Registry Number Reaxys 82200-87-1 CAS Registry Number ChemIDplus Citations Types Sources 2127820 PubMed citation Europe PMC 2155268 PubMed citation Europe PMC 22068350 PubMed citation Europe PMC 26398714 PubMed citation Europe PMC 6806263 PubMed citation Europe PMC Last Modified 22 February 2016