Details
Stereochemistry | RACEMIC |
Molecular Formula | C19H38O4 |
Molecular Weight | 330.5026 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCCCCC(=O)OCC(O)CO
InChI
InChIKey=QHZLMUACJMDIAE-UHFFFAOYSA-N
InChI=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
Molecular Formula | C19H38O4 |
Molecular Weight | 330.5026 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Glyceryl-1-palmitate (α-Monopalmitin, Glycerol 1-hexadecanoate) is a member of the chemical class known as Monoacylglycerols. Glycerol 1-hexadecanoate is found in fats and oils. Glycerol 1-hexadecanoate is a minor component of olive oil and other vegetable oil. α-Monopalmitin is a glycerol esterified fatty acid, monoacylglycerol, found in lipid structures such as ceramides. 1-Palmitoylglycerol may be used as a substrate for the identification and differentiation of enzymes that hydrolyze or transfer monoacylglycerols such as neuropathy target esterase(s) and monoacylglycerol acyltransferase(s) (MAG).
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15513825
Glyceryl-1-palmitate can be used at concentrations up to 12% in cosmetic products
Route of Administration:
Topical
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27497869
The IC50 value of Glyceryl-1-palmitate (α-Monopalmitin), isolated from Alocasia macrorrhiza, was 92.28 ug/ml for HePG2 cells, 36.76 ug/ml for Hep-2 cells and 36.24 ug/ml for HCT-116 cells.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:58:46 UTC 2023
by
admin
on
Fri Dec 15 18:58:46 UTC 2023
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Record UNII |
U9H9OM3S75
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Record Status |
Validated (UNII)
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Record Version |
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