ChemicalBook >> CAS DataBase List >>PF-622

PF-622

CAS No.
898235-65-9
Chemical Name:
PF-622
Synonyms
PF-622;FAAH Inhibitor, PF-622;N-phenyl-4-(quinolin-2-ylmethyl)piperazine-1-carboxamide;1-Piperazinecarboxamide, N-phenyl-4-(2-quinolinylmethyl)-
CBNumber:
CB92454224
Molecular Formula:
C21H22N4O
Molecular Weight:
346.43
MDL Number:
MFCD10567108
MOL File:
898235-65-9.mol
Last updated:2023-05-18 11:31:06

PF-622 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 price More Price(9)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 10010907 PF-622 >98% 898235-65-9 1mg $25 2024-03-01 Buy
Cayman Chemical 10010907 PF-622 >98% 898235-65-9 5mg $107 2024-03-01 Buy
Cayman Chemical 10010907 PF-622 >98% 898235-65-9 10mg $186 2024-03-01 Buy
Cayman Chemical 10010907 PF-622 >98% 898235-65-9 50mg $807 2024-03-01 Buy
ApexBio Technology C4756 PF-622 898235-65-9 50mg $922 2021-12-16 Buy
Product number Packaging Price Buy
10010907 1mg $25 Buy
10010907 5mg $107 Buy
10010907 10mg $186 Buy
10010907 50mg $807 Buy
C4756 50mg $922 Buy

PF-622 Chemical Properties,Uses,Production

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

PF-622 Preparation Products And Raw materials

Raw materials

Preparation Products

PF-622 Suppliers

Global( 26)Suppliers
Supplier Tel Email Country ProdList Advantage
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49739 58
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9709 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8141 58
ApexBio Technology -- sales@apexbt.com United States 6254 58
PF-622 N-phenyl-4-(quinolin-2-ylmethyl)piperazine-1-carboxamide FAAH Inhibitor, PF-622 1-Piperazinecarboxamide, N-phenyl-4-(2-quinolinylmethyl)- 898235-65-9