PF-622 | FAAH inhibitor

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

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

Weight 0.01 mg
Dimensions 0.01 × 0.01 × 0.01 cm
size :

10 mg, 50 mg

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CAS:
898235-65-9
Catalog Number:
10-1299
Activity:
FAAH inhibitor
Chemical Name:
N-Phenyl-4-(quinolin-2-ylmethyl)piperazine-1-carboxamide
Molecular Weight:
346.44
Molecular Formula:
C21H22N4O
Solubility:
Soluble in DMSO (up to 25 mg/ml) or in Ethanol (up to 3 mg/ml).
Physical Properties:
White solid
Purity:
98% by TLC
NMR (Conforms)
Storage Temperature:
RT (des.)
Stability:
Stable for 2 years as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month.
Shipping Code:
RT

PF-622 | FAAH inhibitor

$80.00$320.00

CAS:
898235-65-9
Catalog Number:
10-1299
Activity:
FAAH inhibitor
Chemical Name:
N-Phenyl-4-(quinolin-2-ylmethyl)piperazine-1-carboxamide
Molecular Weight:
346.44
Molecular Formula:
C21H22N4O
Solubility:
Soluble in DMSO (up to 25 mg/ml) or in Ethanol (up to 3 mg/ml).
Physical Properties:
White solid
Purity:
98% by TLC
NMR (Conforms)
Storage Temperature:
RT (des.)
Stability:
Stable for 2 years as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month.
Shipping Code:
RT
  • 10 mg
  • 50 mg
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