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PD-161570

PD-161570
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Purity:99.23%
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PD-161570

Catalog No. T23127Cas No. 192705-80-9
PD-161570 is a potent and ATP-competitive human FGF-1 receptor inhibitor with an IC50 of 39.9 nM and a Ki of 42 nM. It also inhibits the PDGFR, EGFR, and c-Src tyrosine kinases with IC50 values of 310 nM, 240 nM, and 44 nM, respectively.
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Pack SizePriceAvailabilityQuantity
1 mg$98In Stock
2 mg$138In Stock
5 mg$222In Stock
10 mg$328In Stock
25 mg$553In Stock
50 mg$789In Stock
100 mg$1,070In Stock
1 mL x 10 mM (in DMSO)$258In Stock
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Product Introduction

Bioactivity
Description
PD-161570 is a potent and ATP-competitive human FGF-1 receptor inhibitor with an IC50 of 39.9 nM and a Ki of 42 nM. It also inhibits the PDGFR, EGFR, and c-Src tyrosine kinases with IC50 values of 310 nM, 240 nM, and 44 nM, respectively.
Targets&IC50
FGFR1:39.9 nM (IC50), FGFR1 autophosphorylation:622 nM, FGFR1:42 nM (Ki)
AliasPD 161570
Chemical Properties
Molecular Weight532.51
FormulaC26H35Cl2N7O
Cas No.192705-80-9
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 30 mg/mL (56.34 mM), Sonication is recommended.
Ethanol: < 53.25 mg/mL
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8779 mL9.3895 mL18.7790 mL93.8950 mL
5 mM0.3756 mL1.8779 mL3.7558 mL18.7790 mL
10 mM0.1878 mL0.9389 mL1.8779 mL9.3895 mL
20 mM0.0939 mL0.4695 mL0.9389 mL4.6947 mL
50 mM0.0376 mL0.1878 mL0.3756 mL1.8779 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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