PF-622
PF-622 Basic information
- Product Name:
- PF-622
- Synonyms:
-
- PF-622
- N-phenyl-4-(quinolin-2-ylmethyl)piperazine-1-carboxamide
- FAAH Inhibitor, PF-622
- 1-Piperazinecarboxamide, N-phenyl-4-(2-quinolinylmethyl)-
- CAS:
- 898235-65-9
- MF:
- C21H22N4O
- MW:
- 346.43
- Mol File:
- 898235-65-9.mol
PF-622 Chemical Properties
- 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.
PF-622 Usage And Synthesis
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
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
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