CHEBI:75913 - 2-arachidonyl glyceryl ether

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 2-arachidonyl glyceryl ether
ChEBI ID CHEBI:75913
Definition A monoalkylglycerol that is glycerol which is substituted by a (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraen-1-yl group at position 2.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter laimo
Supplier Information ZINC000008860490
Download Molfile XML SDF
more structures >>
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C23H40O3
Net Charge 0
Average Mass 364.56190
Monoisotopic Mass 364.29775
InChI InChI=1S/C23H40O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-26-23(21-24)22-25/h6-7,9-10,12-13,15-16,23-25H,2-5,8,11,14,17-22H2,1H3/b7-6-,10-9-,13-12-,16-15-
InChIKey CUJUUWXZAQHCNC-DOFZRALJSA-N
SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCOC(CO)CO
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via endocannabinoid )
cannabinoid receptor agonist
An agonist that binds to and activates cannabinoid receptors.
(via cannabinoid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-arachidonyl glyceryl ether (CHEBI:75913) is a 2-alkylglycerol (CHEBI:76581)
2-arachidonyl glyceryl ether (CHEBI:75913) is a endocannabinoid (CHEBI:67197)
2-arachidonyl glyceryl ether (CHEBI:75913) is a monoalkylglycerol (CHEBI:75883)
IUPAC Name
2-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraen-1-yloxy]propane-1,3-diol
Synonyms Sources
(5Z,8Z,11Z,14Z)-icosatetraenyl-2-glyceryl ether SUBMITTER
2-(5Z,8Z,11Z,14Z-eicosatetraenyl)-sn-glycerol LIPID MAPS
2-AG ether LIPID MAPS
2-arachidonyl glycerol ether ChEBI
2-O-(5Z,8Z,11Z,14Z)-eicosatetraenylglycerol UniProt
5Z,8Z,11Z,14Z-eicosatetraen-2-glyceryl ether LIPID MAPS
noladin ether LIPID MAPS
Manual Xrefs Databases
2-Arachidonyl_glyceryl_ether Wikipedia
HMDB0013657 HMDB
LMGL01010029 LIPID MAPS
View more database links
Registry Numbers Types Sources
222723-55-9 CAS Registry Number HMDB
8798140 Reaxys Registry Number Reaxys
Citations Types Sources
11259648 PubMed citation Europe PMC
22309979 PubMed citation Europe PMC
22728691 PubMed citation Europe PMC
23386378 PubMed citation Europe PMC
Last Modified
12 February 2019