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PF-06260933

SKU: orb1303048

Description

PF-06260933

Research Area

Signal Transduction

Images & Validation

Key Properties

CAS Number1811510-56-1
MW296.75
Purity99.63%
FormulaC16H13ClN4
SMILESNc1ccc(cn1)-c1cnc(N)c(c1)-c1ccc(Cl)cc1
TargetMAPK
SolubilityDMSO:50 mg/mL (168.49 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (6.74 mM)

Bioactivity

Target IC50
MAP4K4:3.7 nM
In Vivo
Treatment with PF-06260933 does not modify plasma lipid content in a mouse model, yet it leads to decreased glucose levels, mirroring outcomes seen in whole-body-inducible Map4k4 knockout animals. Moreover, PF-06260933 administration results in eithe the attenuation of plaque progression or promotion of plaque regression in this model (46.0% versus 25.5%), alongside reductions In both plasma glucose and lipid content.
In Vitro
Treatment with PF-06260933 significantly enhance the resistance of human aortic endothelial cells (EC) to TNF-α-induced increases in endothelial permeability in vitro

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
DisclaimerFor research use only

Alternative Names

Inhibitor, MAPK Kinase Kinase Kinase, MAP4K, MAP4K4 for Cell, MAP4K4 for Kinase, inhibit, PF6260933, PF-6260933, PF06260933, PF-06260933, PF 6260933, PF 06260933

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  • PF-06260933 [orb1225883]

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    1811510-56-1

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    C16H13ClN4

    1 g, 500 mg, 25 mg, 50 mg, 100 mg, 200 mg, 10 mg, 2 mg, 5 mg
Quality Guarantee

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Key Properties

No computed properties available.

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Protocol Information

PF-06260933 (orb1303048)

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Step 1: Enter information below

(Recommended: An additional animal making an allowance for loss during the experiment)

Step 2: Enter the in vivo formulation

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

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1 mg
$ 90.00
2 mg
$ 100.00
1 ml x 10 mM (in DMSO)
$ 150.00
5 mg
$ 150.00
10 mg
$ 210.00
25 mg
$ 390.00
50 mg
$ 590.00
100 mg
$ 830.00
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