CHEBI:136500 - 14(R),15(S)-DiHETE

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ChEBI Name 14(R),15(S)-DiHETE ChEBI ID CHEBI:136500 ChEBI ASCII Name 14(R),15(S)-DiHETE Definition A DiHETE that is (5Z,8Z,10E,12E)-icosatetraenoic acid carrying two hydroxy substituents at positions 14 and 15 (the 14R,15S-stereoisomer). 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/c1-2-3-12-15-18(21)19(22)16-13-10-8-6-4-5-7-9-11-14-17-20(23)24/h4,6-10,13,16,18-19,21-22H,2-3,5,11-12,14-15,17H2,1H3,(H,23,24)/b6-4-,9-7-,10-8+,16-13+/t18-,19+/m0/s1 InChIKey RFCYXKNVYQOCTM-PEPUZGFWSA-N SMILES OC(CCC/C=C\C/C=C\C=C\C=C\[C@H]([C@H](CCCCC)O)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. View more via ChEBI Ontology ChEBI Ontology Outgoing 14(R),15(S)-DiHETE (CHEBI:136500) has role human xenobiotic metabolite (CHEBI:76967) 14(R),15(S)-DiHETE (CHEBI:136500) is a dihydroxyicosatetraenoic acid (CHEBI:72868) 14(R),15(S)-DiHETE (CHEBI:136500) is conjugate acid of 14(R),15(S)-DiHETE(1−) (CHEBI:133916) Incoming 14(R),15(S)-DiHETE(1−) (CHEBI:133916) is conjugate base of 14(R),15(S)-DiHETE (CHEBI:136500) IUPAC Name (5Z,8Z,10E,12E,14R,15S)-14,15-dihydroxyicosa-5,8,10,12-tetraenoic acid Synonyms Sources (14R,15S)-DiHETE ChEBI (14R,15S)-dihydroxy-(5Z,8Z,10E,12E)-eicosatetraenoic acid ChEBI (14R,15S)-dihydroxy-(5Z,8Z,10E,12E)-icosatetraenoic acid ChEBI (5Z,8Z,10E,12E,14R,15S)-14,15-dihydroxyeicosatetraenoic acid ChEBI (5Z,8Z,10E,12E,14R,15S)-14,15-dihydroxyicosatetraenoic acid ChEBI Registry Number Type Source 4704842 Reaxys Registry Number Reaxys Citation Type Source 8334154 PubMed citation Europe PMC Last Modified 08 March 2017