CHEBI:82929 - 1,2-dipalmitoyl-sn-glycerol

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ChEBI Name 1,2-dipalmitoyl-sn-glycerol
ChEBI ID CHEBI:82929
ChEBI ASCII Name 1,2-dipalmitoyl-sn-glycerol
Definition A 1,2-diacyl-sn-glycerol in which both acyl groups are specified as palmitoyl (hexadecanoyl).
Stars This entity has been manually annotated by the ChEBI Team.
Submitter laimo
Supplier Information
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Formula C35H68O5
Net Charge 0
Average Mass 568.91140
Monoisotopic Mass 568.50668
InChI InChI=1S/C35H68O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-34(37)39-32-33(31-36)40-35(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h33,36H,3-32H2,1-2H3/t33-/m0/s1
InChIKey JEJLGIQLPYYGEE-XIFFEERXSA-N
SMILES CCCCCCCCCCCCCCCC(=O)OC[C@H](CO)OC(=O)CCCCCCCCCCCCCCC
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: MetaboLights Study
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
(via diglyceride )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via diglyceride )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1,2-dipalmitoyl-sn-glycerol (CHEBI:82929) has role mouse metabolite (CHEBI:75771)
1,2-dipalmitoyl-sn-glycerol (CHEBI:82929) is a 1,2-diacyl-sn-glycerol (CHEBI:17815)
1,2-dipalmitoyl-sn-glycerol (CHEBI:82929) is a 1,2-dipalmitoylglycerol (CHEBI:78090)
IUPAC Name
(2S)-3-hydroxypropane-1,2-diyl dihexadecanoate
Synonyms Sources
(S)-1-(Hydroxymethyl)ethane-1,2-diyl dipalmitate ChemIDplus
1,2-dihexadecanoyl-sn-glycerol UniProt
DAG(16:0/16:0) HMDB
DAG(32:0) HMDB
DG(16:0/16:0) HMDB
DG(16:0/16:0/0:0) LIPID MAPS
DG(32:0) HMDB
Diacylglycerol(16:0/16:0) HMDB
Diacylglycerol(32:0) HMDB
Manual Xrefs Databases
HMDB0007098 HMDB
LMGL02010009 LIPID MAPS
View more database links
Registry Numbers Types Sources
30334-71-5 CAS Registry Number ChemIDplus
3597346 Reaxys Registry Number Reaxys
Last Modified
23 October 2015