Cat. No. 1815
Alternative Name: PIA
Chemical Name: N-(1-Methylethyl)-hexadecanamide
Biological ActivityInhibitor of fatty acid amide hydrolase (FAAH); pIC50 = 4.89 for inhibition of [3H]-anandamide metabolism. Displays little binding to CB1 and CB2 receptors (IC50 > 100 μM) and very weakly blocks anandamide uptake (IC50 ~ 100 μM). Inhibits proliferation of C6 glioma cells.
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Certificate of Analysis / Safety Data Sheet
Jonsson et al (2001) Effects of homologues and analogues of palmitoylethanolamide upon the inactivation of the endocannabinoid anandamide. Br.J.Pharmacol. 133 1263. PMID: 11498512.
Jonsson et al (2003) AM404 and VDM 11 non-specifically inhibit C6 glioma cell proliferation at concentrations used to block the cellular accumulation of the endocannabinoid anandamide. Arch.Toxicol. 77 201. PMID: 12698235.
If you know of a relevant citation for this product please let us know.
View Related Products by Target
Keywords: Palmitoylisopropylamide, supplier, inhibitors, FAAH, cannabinoids, Receptors, Anandamide, Amidase, Fatty, Acid, Amide, Hydrolases
Find multiple products by catalog number
New Products in this Area
Potent and selective CB1 receptor antagonistCOR 170
Selective CB2 receptor inverse agonist
Meet your representative
July 15, 2014