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CHEBI:69081 - 1-monopalmitoylglycerol

Default Structure
ChEBI IDCHEBI:69081
ChEBI Name1-monopalmitoylglycerol
Stars
DefinitionA 1-monoglyceride that has palmitoyl as the acyl group. A natural product found in Neolitsea daibuensis.
Last Modified17 May 2017
DownloadsMolfile
FormulaC19H38O4
Net Charge0
Average Mass330.509
Monoisotopic Mass330.27701
SMILESCCCCCCCCCCCCCCCC(=O)OCC(O)CO
InChIInChI=1S/C19H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(22)23-17-18(21)16-20/h18,20-21H,2-17H2,1H3
InChIKeyQHZLMUACJMDIAE-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Chlamydomonas reinhardtii (ncbitaxon:3055) - PubMed (25515814)
Neolitsea daibuensis (IPNI:466954-1) root (BTO:0001188) PubMed (22148193) Cold MeOH extract of dried roots
Roles Classification
Biological Roles:
algal metabolite  Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
ChEBI Ontology
Outgoing Relation(s)
1-monopalmitoylglycerol (CHEBI:69081) has functional parent hexadecanoic acid (CHEBI:15756)
1-monopalmitoylglycerol (CHEBI:69081) has role algal metabolite (CHEBI:84735)
1-monopalmitoylglycerol (CHEBI:69081) has role plant metabolite (CHEBI:76924)
1-monopalmitoylglycerol (CHEBI:69081) is a 1-acylglycerol 16:0 (CHEBI:134127)
Incoming Relation(s)
1-hexadecanoyl-sn-glycerol (CHEBI:75542) is a 1-monopalmitoylglycerol (CHEBI:69081)
3-palmitoyl-sn-glycerol (CHEBI:64757) is a 1-monopalmitoylglycerol (CHEBI:69081)
IUPAC Name 
2,3-dihydroxypropyl palmitate
Synonyms  Source
1-palmitoylglycerolChemIDplus
2,3-dihydroxypropyl hexadecanoateChEBI
glycerol 1-monopalmitateChemIDplus
glycerol 1-palmitateChemIDplus
glycerol 3-palmitateChemIDplus
glyceryl palmitateChemIDplus
UniProt Name  Source
1-hexadecanoylglycerolUniProt
Manual XrefsDatabases
CPD-8508MetaCyc
HMDB0031074HMDB
LSM-4482LINCS
Registry NumbersSources
Reaxys:1728235Reaxys
CAS:542-44-9ChemIDplus
Citations