2-MONOPALMITIN

2-MONOPALMITIN Basic information
Product Name:2-MONOPALMITIN
Synonyms:2-monopalmitoylglycerol (C16:0);2-O-Hexadecanoylglycerol;2-O-Palmitoylglycerol;2-O-Palmitoyl-L-glycerol;Hexadecanoic acid [2-hydroxy-1-(hydroxymethyl)ethyl] ester;Palmitic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester;2-(1,3-dihydroxypropan-2-yl)hexadecanoic acid compound with 1,3-dihydroxypropan-2-yl palmitate (1:1);2-Hexadecanoylglycerol
CAS:23470-00-0
MF:C19H38O4
MW:330.5
EINECS:
Product Categories:Fatty Acid Derivatives & Lipids;Glycerols;Cannabinoid receptor;SiChem
Mol File:23470-00-0.mol
2-MONOPALMITIN Structure
2-MONOPALMITIN Chemical Properties
Melting point 68-70°C
Boiling point 387.92°C (rough estimate)
density 0.9708 (rough estimate)
refractive index 1.4434 (estimate)
storage temp. −20°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
pka13.54±0.10(Predicted)
form neat
color White to Off-White
BRN 1796692
Safety Information
Hazard Codes Xi
Risk Statements 43
Safety Statements 36/37
WGK Germany 3
MSDS Information
2-MONOPALMITIN Usage And Synthesis
Description2-Arachidonoyl glycerol (2-AG; ) is an endogenous agonist of the CB1 and CB2 cannabinoid receptors. 2-Palmitoyl glycerol is a fatty acid ester that does not bind directly to cannabinoid receptors, nor inhibit adenylyl cyclase, but rather potentiates the activity of 2-AG (and other endocannabinoids) to bind to CB1 and CB2 and inhibit adenylyl cyclase. This “entourage” effect has been attributed to blockade of the breakdown and reuptake pathways that normally function to reduce endocannabinoid levels rapidly upon release. 2-Palmitoyl glycerol and related endogenous fatty acid derivatives have been shown to interact with endocannabinoids in the modulation of pain sensitivity.
Chemical PropertiesWhite Solid
UsesA biomarker of metabolic responses to hepatotoxicants and carcinogens.
DefinitionChEBI: A 2-monoglyceride where the acyl group is hexadecanoyl (palmitoyl).
Biological ActivityEndogenous fatty acid glycerol ester that enhances activity of 2-arachidonylglycerol ((5Z,8Z,11Z,14Z)-5,8,11,14-Eicosatetraenoic acid,2-hydroxy-1-(hydroxymethyl)ethyl ester ). Does not bind to CB 1 or CB 2 cannabinoid receptors, but potentiates the apparent binding of 2-AG and increases its ability to inhibit adenylyl cyclase. Enhances in vivo cannabinoid effects of 2-AG following combined administration with 2-linoleoylglycerol.
2-MONOPALMITIN Preparation Products And Raw materials
1,2-DIPALMITOYL-SN-GLYCERO-3-PHOSPHATE CALCIUM SALT 1,2-DIHEXADECANOYL-SN-GLYCERO-3-[BIS(PHENYL) PHOSPHATE] TRIARACHIDIN 1,2-DIHEXADECANOYL-SN-GLYCERO-3-PHOSPHO[N-HEXADECANOYL]ETHANOLAMINE AMMONIUM SALT 1,2-DIPALMITOYL-RAC-GLYCEROL L-ALPHA-PHOSPHATIDYLCHOLINE, DISTEAROYL 1,2-DIPALMITOYL-3-O-HEXADECYL-RAC-GLYCEROL 2-MONOOLEIN 1,2-DIARACHIDIN 1,2-DIHEXADECANOYL-RAC-GLYCERO-3-PHOSPHO[DIMETHYLAMINOETHANOL] DELTA 9 CIS MONOOLEIN,DL-ALPHA-MONOOLEIN,1-MONOOLEIN,MONOOLEIN,di-alpha-monoolein 1,2-DIPALMITOYL-SN-GLYCERO-3-PHOSPHOCHOLINE TRIHEPTADECANOIN 1,2-DIPALMITOYL-SN-GLYCERO-3-PHOSPHO-(N-METHYL)-ETHANOLAMINE 1,2-DIPALMITOYL-3-OLEOYL-RAC-GLYCEROL 1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE 1,2-DIPALMITOYL-SN-GLYCERO-3-PHOSPHATE 1,2-DIPALMITOYL-3-O-BENZYL-RAC-GLYCEROL

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