CHEBI:34484 - 8(R)-HETE

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ChEBI Name 8(R)-HETE ChEBI ID CHEBI:34484 ChEBI ASCII Name 8(R)-HETE Definition A HETE having an (8R)-hydroxy group and (5Z)-, (9E)-, (11Z)- and (14Z)-double bonds. 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 320.46628 Monoisotopic Mass 320.23514 InChI InChI=1S/C20H32O3/c1-2-3-4-5-6-7-8-9-10-13-16-19(21)17-14-11-12-15-18-20(22)23/h6-7,9-11,13-14,16,19,21H,2-5,8,12,15,17-18H2,1H3,(H,22,23)/b7-6-,10-9-,14-11-,16-13+/t19-/m0/s1 InChIKey NLUNAYAEIJYXRB-GTYUHVKWSA-N SMILES CCCCC\C=C/C\C=C/C=C/[C@H](O)C\C=C/CCCC(O)=O Roles Classification Chemical Role(s): Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) View more via ChEBI Ontology ChEBI Ontology Outgoing 8(R)-HETE (CHEBI:34484) has functional parent icosa-5,9,11,14-tetraenoic acid (CHEBI:36042) 8(R)-HETE (CHEBI:34484) is a HETE (CHEBI:36275) 8(R)-HETE (CHEBI:34484) is enantiomer of 8(S)-HETE (CHEBI:34486) Incoming 8(S)-HETE (CHEBI:34486) is enantiomer of 8(R)-HETE (CHEBI:34484) IUPAC Name (5Z,8R,9E,11Z,14Z)-8-hydroxyicosa-5,9,11,14-tetraenoic acid Synonyms Sources (+)-(8R,5Z,9E,11Z,14Z)-8-hydroxy-5,9,11,14-eicosatetraenoic acid ChEBI (+)-(8R,5Z,9E,11Z,14Z)-8-hydroxy-5,9,11,14-icosatetraenoic acid ChEBI (5Z,8R,9E,11Z,14Z)-8-hydroxyeicosa-5,9,11,14-tetraenoic acid ChEBI (5Z,9E,11Z,14Z)-(8R)-8-Hydroxyeicosa-5,9,11,14-tetraenoic acid KEGG COMPOUND (5Z,9E,11Z,14Z)-(8R)-8-Hydroxyicosa-5,9,11,14-tetraenoic acid KEGG COMPOUND (8R)-hydroxy-(5Z),(9E),(11Z),(14Z)-eicosatetraenoic acid ChEBI (R)-(Z,E,Z,Z)-8-hydroxyeicosa-5,9,11,14-tetraenoic acid ChEBI 8(R)-HETE KEGG COMPOUND 8(R)-hydroxyeicosatetraenoic acid ChEBI 8R-HETE LIPID MAPS Manual Xrefs Databases C14824 KEGG COMPOUND LMFA03060021 LIPID MAPS View more database links Registry Number Type Source 4688096 Reaxys Registry Number Reaxys Citation Type Source 3097019 PubMed citation Europe PMC Last Modified 28 March 2011

General Comment 2011-03-23 8(R)-HETE is biosynthesized by lipoxygenation of arachidonic acid in marine invertebrates such as gorgonian corals and starfish.