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HomeProduct name listPF-622

PF-622

PF-622 Structural

What is PF-622?

Description

PF-622 (898235-65-9) is a potent and selective irreversible FAAH inhibitor. Covalently modifies active site-serine (IC50=33 nM). Completely selective for FAAH relative to other mammalian serine hydrolases. Cell permeable

What are the applications of Application

PF-622 is a novel, potent and selective inhibitor of FAAH (fatty acid amide hydrolase)

in vitro

pf-622 inhibited the activity of faah in a time-dependent manner with the ic50 values of 0.99 and 0.033 μm in human recombinant faah for 5 and 60 minutes, respectively [1]. in various human and murine tissue proteome samples, pf-622 showed highly selectivity for faah in relative to other serine hydrolases, showing no discernable off-site activity up to 500 μm [1]. pf-622 at 1 μm decreased il-2 production in both healthy subjects and in hcv patients [2].

References

1) Ahn et al. (2007), Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity; Biochemistry, 46 13019

Properties of PF-622

storage temp.  RT
solubility  Soluble in DMSO (up to 25 mg/ml) or in Ethanol (up to 3 mg/ml).
form  Off-white solid.
color  White
Stability: Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month.

Safety information for PF-622

Computed Descriptors for PF-622

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