CHEBI:63974 - 5,6-DHET

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 5,6-DHET
ChEBI ID CHEBI:63974
Definition A DHET obtained by formal dihydroxylation across the 5,6-double bond of arachidonic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Mark Williams
Secondary ChEBI IDs CHEBI:34449
Supplier Information eMolecules:636962, ZINC000100044649
Download Molfile XML SDF
Formula C20H34O4
Net Charge 0
Average Mass 338.48160
Monoisotopic Mass 338.24571
InChI InChI=1S/C20H34O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-18(21)19(22)16-14-17-20(23)24/h6-7,9-10,12-13,18-19,21-22H,2-5,8,11,14-17H2,1H3,(H,23,24)/b7-6-,10-9-,13-12-
InChIKey GFNYAPAJUNPMGH-QNEBEIHSSA-N
SMILES CCCCC\C=C/C\C=C/C\C=C/CC(O)C(O)CCCC(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: MetaboLights Study
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 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): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via DHET )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5,6-DHET (CHEBI:63974) has role mouse metabolite (CHEBI:75771)
5,6-DHET (CHEBI:63974) is a DHET (CHEBI:64005)
IUPAC Name
(8Z,11Z,14Z)-5,6-dihydroxyicosa-8,11,14-trienoic acid
Synonyms Sources
(+/-)5,6-DiHETrE LIPID MAPS
(8Z,11Z,14Z)-5,6-Dihydroxyeicosa-8,11,14-trienoic acid KEGG COMPOUND
(8Z,11Z,14Z)-5,6-Dihydroxyicosa-8,11,14-trienoic acid KEGG COMPOUND
5,6-DHET KEGG COMPOUND
5,6-DiHETrE SUBMITTER
5,6-dihydroxy-8Z,11Z,14Z-eicosatrienoic acid LIPID MAPS
5,6-dihydroxy-8Z,11Z,14Z-icosatrienoic acid ChEBI
Manual Xrefs Databases
C14772 KEGG COMPOUND
HMDB0002343 HMDB
LMFA03050004 LIPID MAPS
View more database links
Registry Numbers Types Sources
213382-49-1 CAS Registry Number HMDB
8580625 Reaxys Registry Number Reaxys
Citation Type Source
9694933 PubMed citation Europe PMC
Last Modified
27 January 2016