PF-622

PF-622 Suppliers list
Company Name: Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel: +86-057181025280; +8617767106207
Email: sales@molcore.com
Products Intro: Product Name:PF-622
CAS:898235-65-9
Purity:NLT 98% Remarks:MC578502
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Products Intro: Product Name:PF-622
CAS:898235-65-9
Purity:>98% Package:5mg;25mg
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:PF-622
CAS:898235-65-9
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
Company Name: MedBioPharmaceutical Technology Inc  
Tel: 021-69568360 18916172912
Email: order@med-bio.cn
Products Intro: Product Name:PF-622
CAS:898235-65-9
Purity:98% Package:50mg; 5mg; 10mg Remarks:Medbio
Company Name: ApexBio Technology  
Tel: + 1-832-696-8203
Email: sales@apexbt.com
Products Intro: Product Name:PF-622
CAS:898235-65-9
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
EINECS:
Product Categories:
Mol File:898235-65-9.mol
PF-622 Structure
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.
Safety Information
MSDS Information
PF-622 Usage And Synthesis
DescriptionPF-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 vitropf-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].
References1) 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
Tag:PF-622(898235-65-9) Related Product Information
Prostaglandin E2 6-ISOPROPOXY-9-XANTHONE-2-CARBOXYLIC ACID URB597 LY 171883 PF-622