[CAS NO. 1467057-23-3]  PF-06409577

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PRODUCTS SPECIFICATIONS [1467057-23-3]

Store
Catalog
SLK-S8335
Brand
Selleck
CAS
1467057-23-3

DESCRIPTION [1467057-23-3]

Overview

MDLMFCD29917835
Molecular Weight341.79
Molecular FormulaC19H16ClNO3
SMILESO=C(C1=CNC2=C1C=C(C3=CC=C(C4(O)CCC4)C=C3)C(Cl)=C2)O

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Description

PF-06409577 is an orally bioavailable activator with of 7 nM for α1β1γ1 in the TR-FRET assay and it shows no detectable inhibition of hERG in a patch-clamp assay (100 μM) and was not an inhibitor (IC50 > 100 μM) of the microsomal activities of major human cytochrome P450 isoforms.

Targets

AMPK α2β1γ1 [1]AMPK α1β1γ1 [1]
6.8 nM(EC50)7 nM(EC50)

In vitro

PF-06409577 activates α1β1γ1 and α2β1γ1 AMPK isoforms with EC50 of 7.0 nM and 6.8 nM but was much less active against α1β2γ1/α2β2γ1/α2β2γ3 AMPK isoforms with EC50 greater 4000 nM.

In vivo

PF-06409577 exhibits efficacy in a preclinical model of diabetic nephropathy. It exhibits high plasma protein binding in rat (plasma unbound fraction, fu,p = 0.0044), dog (fu,p = 0.028), monkey (fu,p = 0.032), and human (fu,p = 0.017). Following iv administration, PF-06409577 demonstrates moderate plasma clearance (CLp) in rats (22.6 mL/min/kg), dogs (12.9 mL/min/kg), and monkeys (8.57 mL/min/kg) and was well distributed with steady state distribution volumes (Vdss) ranging from 0.846-3.15 L/kg. Following oral administration of crystalline PF-06409577 in 0.5% methylcellulose suspension, PF-06409577 is rapidly absorbed (Tmax = 0.25-1.20 h) in rats, dogs, and monkeys. The corresponding oral bioavailability (F) values in rats, dogs, and monkeys, were 15%, 100%, and 59%, respectively. PF-06409577 is subject to a higher degree of first pass intestinal glucuronidation in the rat (relative to other preclinical species and human).