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
| Size | Price / USD | Stock | Quantity |
| 2MG | 34 | In Stock |
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| 5MG | 55 | In Stock |
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| 10MG | 96 | In Stock |
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| 25MG | 200 | In Stock |
|
| 50MG | 362 | In Stock |
|
| 100MG | 538 | In Stock |
|
| 500MG | 1161 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NamePF-06409577
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NoteResearch use only, not for human use.
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Brief DescriptionPF-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.
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DescriptionPF-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.
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In Vitro——
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In Vivo——
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SynonymsPF 06409577 | PF06409577 | PF 6409577
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PathwayMembrane Transporter/Ion Channel
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TargetAMPK
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RecptorAMPKα1β1γ1
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Research AreaMetabolic Disease
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IndicationDiabetes
Chemical Information
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CAS Number1467057-23-3
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Formula Weight341.79
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Molecular FormulaC19H16ClNO3
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Purity>98% (HPLC)
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SolubilityDMSO: 34.2 mg/mL (100 mM); Ethanol: 6.8 mg/mL (20 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
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SMILESO=C(C1=CNC2=C1C=C(C3=CC=C(C4(O)CCC4)C=C3)C(Cl)=C2)O
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Chemical Name6-Chloro-5-[4-(1- hydroxycyclobutyl)phenyl]-1H-indole-3-carboxylic acid
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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