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CHEBI:34162 - 16(R)-HETE

ChEBI IDCHEBI:34162
ChEBI Name16(R)-HETE
Stars
ASCII Name16(R)-HETE
DefinitionA 16-HETE in which the chiral centre at position 16 has R-configuration.
Last Modified9 August 2017
DownloadsMolfile
FormulaC20H32O3
Net Charge0
Average Mass320.473
Monoisotopic Mass320.23514
SMILESCCCC[C@@H](O)/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O
InChIInChI=1S/C20H32O3/c1-2-3-16-19(21)17-14-12-10-8-6-4-5-7-9-11-13-15-18-20(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-/m1/s1
InChIKeyJEKNPVYFNMZRJG-STHMYGMFSA-N
Species of MetaboliteComponentSourceComments
Mus musculus (ncbitaxon:10090) - PubMed (19425150) Source: BioModels - MODEL1507180067
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
ChEBI Ontology
Outgoing Relation(s)
16(R)-HETE (CHEBI:34162) has role mouse metabolite (CHEBI:75771)
16(R)-HETE (CHEBI:34162) is a 16-HETE (CHEBI:63994)
16(R)-HETE (CHEBI:34162) is conjugate acid of 16(R)-HETE(1−) (CHEBI:137166)
16(R)-HETE (CHEBI:34162) is enantiomer of 16(S)-HETE (CHEBI:138110)
Incoming Relation(s)
16(R)-HETE(1−) (CHEBI:137166) is conjugate base of 16(R)-HETE (CHEBI:34162)
16(S)-HETE (CHEBI:138110) is enantiomer of 16(R)-HETE (CHEBI:34162)
IUPAC Name 
(5Z,8Z,11Z,14Z,16R)-16-hydroxyicosa-5,8,11,14-tetraenoic acid
Synonyms  Source
16(R)-HETEKEGG COMPOUND
(5Z,8Z,11Z,14Z)-(16R)-16-Hydroxyeicosa-5,8,11,14-tetraenoic acidKEGG COMPOUND
(5Z,8Z,11Z,14Z)-(16R)-16-Hydroxyicosa-5,8,11,14-tetraenoic acidKEGG COMPOUND
(all-Z)-16(R)-hydroxy-5,8,11,14-eicosatetraenoic acidChEBI
16(R)-hydroxyeicosa-5(Z),8(Z),11(Z),14(Z)-tetraenoic acidChEBI
(16R,5Z,8Z,11Z,14Z)-16-hydroxy-5,8,11,14-eicosatetraenoic acidChEBI
Manual XrefsDatabases
C14778KEGG COMPOUND
LMFA03060069LIPID MAPS
Registry NumbersSources
Reaxys:9287647Reaxys
Citations