PF-06409577

CAS No. 1467057-23-3

PF-06409577( PF 06409577 | PF06409577 | PF 6409577 )

Catalog No. M11999 CAS No. 1467057-23-3

PF-06409577(PF06409577, PF 6409577)?is a potent, selective AMPK β1-containing isoforms activator with TR-FRET EC50 of 7.0 and 6.8 nM for α1β1γ1 and α2β1γ1, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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2MG 34 In Stock
5MG 55 In Stock
10MG 96 In Stock
25MG 200 In Stock
50MG 362 In Stock
100MG 538 In Stock
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Biological Information

  • Product Name
    PF-06409577
  • Note
    Research use only, not for human use.
  • Brief Description
    PF-06409577(PF06409577, PF 6409577)?is a potent, selective AMPK β1-containing isoforms activator with TR-FRET EC50 of 7.0 and 6.8 nM for α1β1γ1 and α2β1γ1, respectively.
  • Description
    PF-06409577(PF06409577, PF 6409577)?is a potent, selective AMPK β1-containing isoforms activator with TR-FRET EC50 of 7.0 and 6.8 nM for α1β1γ1 and α2β1γ1, respectively; displays no activity for α1β2γ1/α2β2γ1/α2β2γ3 with EC50 >40 uM; elevates the phosphorylation of AMPK in the kidney, without impacting blood glucose levels, and reduces the progression of proteinuria in rat model of diabetic nephropathy.Diabetes Phase 1 Discontinued(In Vitro):PF-06409577 possesses similar potency toward the human and rat α1β1γ1 isoforms. In broad panel screening against other receptors, channels, PDEs and kinases, PF-06409577 exhibits minimal off-target pharmacology. PF-06409577 shows no detectable inhibition of hERG in a patch-clamp assay (100 μM) and is not an inhibitor (IC50>100 μM) of the microsomal activities of major human cytochrome P450 isoforms.(In Vivo):PF-06409577 demonstrates moderate plasma clearance in rats, dogs, and monkeys, and is well distributed with steady state distribution volume. Following oral administration of crystalline PF-06409577 in 0.5% methylcellulose suspension, PF-06409577 is rapidly absorbed in rats, dogs, and monkeys. The corresponding oral bioavailability values in rats, dogs, and monkeys, are 15%, 100%, and 59%, respectively. Dose responsive increases in pAMPK relative to total AMPK (tAMPK) in whole kidney tissue are observed with a maximal 3.8-fold response at 300 mg/kg PF-06409577 treatment. Oral administration of PF-06409577 (10, 30, and 100 mg/kg QD) results in dose-dependent reductions in proteinuria in the obese ZSF1 animals, with greater than 2-fold reduction in 24-hour urinary albumin loss compared to vehicle control after 60 days of treatment.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    PF 06409577 | PF06409577 | PF 6409577
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    AMPK
  • Recptor
    AMPKα1β1γ1
  • Research Area
    Metabolic Disease
  • Indication
    Diabetes

Chemical Information

  • CAS Number
    1467057-23-3
  • Formula Weight
    341.79
  • Molecular Formula
    C19H16ClNO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 34.2 mg/mL (100 mM); Ethanol: 6.8 mg/mL (20 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
  • SMILES
    O=C(C1=CNC2=C1C=C(C3=CC=C(C4(O)CCC4)C=C3)C(Cl)=C2)O
  • Chemical Name
    6-Chloro-5-[4-(1- hydroxycyclobutyl)phenyl]-1H-indole-3-carboxylic acid

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Cameron KO, et al. J Med Chem. 2016 Sep 8;59(17):8068-81. 2. Salatto CT, et al. J Pharmacol Exp Ther. 2017 May;361(2):303-311.
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