EMBL-EBI | Chemical Biology | ChEBI

Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search

CHEBI:34126 - 11(R)-HETE

ChEBI IDCHEBI:34126
ChEBI Name11(R)-HETE
Stars
ASCII Name11(R)-HETE
DefinitionAn 11-HETE in which the chiral centre at position 11 has R-configuration.
Secondary ChEBI IDCHEBI:78835
Last Modified30 August 2017
Submitternhn
DownloadsMolfile
FormulaC20H32O3
Net Charge0
Average Mass320.473
Monoisotopic Mass320.23514
SMILESCCCCC/C=C\C=C\[C@H](O)C/C=C\C/C=C\CCCC(=O)O
InChIInChI=1S/C20H32O3/c1-2-3-4-5-7-10-13-16-19(21)17-14-11-8-6-9-12-15-18-20(22)23/h6-7,9-11,13-14,16,19,21H,2-5,8,12,15,17-18H2,1H3,(H,22,23)/b9-6-,10-7-,14-11-,16-13+/t19-/m0/s1
InChIKeyGCZRCCHPLVMMJE-WXMXURGXSA-N
Roles Classification
Chemical Roles:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
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)
11(R)-HETE (CHEBI:34126) is a 11-HETE (CHEBI:72606)
11(R)-HETE (CHEBI:34126) is conjugate acid of 11(R)-HETE(1−) (CHEBI:78836)
11(R)-HETE (CHEBI:34126) is enantiomer of 11(S)-HETE (CHEBI:138332)
Incoming Relation(s)
2-[(11R)-hydroxy-(5Z,8Z,12E,14Z)-icosatetraenoyl]-sn-glycero-3-phosphoethanolamine (CHEBI:138339) has functional parent 11(R)-HETE (CHEBI:34126)
11(R)-HETE(1−) (CHEBI:78836) is conjugate base of 11(R)-HETE (CHEBI:34126)
11(S)-HETE (CHEBI:138332) is enantiomer of 11(R)-HETE (CHEBI:34126)
IUPAC Name 
(5Z,8Z,11R,12E,14Z)-11-hydroxyicosa-5,8,12,14-tetraenoic acid
Synonyms  Source
11(R)-HETEKEGG COMPOUND
(5Z,8Z,12E,14Z)-(11R)-Hydroxyeicosa-5,8,12,14-tetraenoic acidKEGG COMPOUND
(5Z,8Z,12E,14Z)-(11R)-Hydroxyicosa-5,8,12,14-tetraenoic acidKEGG COMPOUND
11R-HETELIPID MAPS
(11R)-hydroxy-(5Z),(8Z),(12E),(14Z)-eicosatetraenoic acidChEBI
11(R)-hydroxyeicosatetraenoic acidChEBI
Manual XrefsDatabases
C14780KEGG COMPOUND
LMFA03060028LIPID MAPS
C00000425KNApSAcK
Registry NumbersSources
Reaxys:5277419Reaxys
CAS:73347-43-0KEGG COMPOUND
Citations