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AZ13705339

AZ13705339
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Purity:98.57%
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AZ13705339

Catalog No. T26704Cas No. 2016806-57-6
AZ13705339 is an effective inhibitor of PAK1 with an IC50 of 0.33 nM and a Kd of 0.28 nM. AZ13705339 binds PAK2 with a Kd of 0.32 nM. AZ13705339 can be used in studies about cancers.
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Pack SizePriceAvailabilityQuantity
2 mg$39In Stock
5 mg$64In Stock
10 mg$98In Stock
25 mg$222In Stock
50 mg$355In Stock
100 mg$572In Stock
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Product Introduction

Bioactivity
Description
AZ13705339 is an effective inhibitor of PAK1 with an IC50 of 0.33 nM and a Kd of 0.28 nM. AZ13705339 binds PAK2 with a Kd of 0.32 nM. AZ13705339 can be used in studies about cancers.
In vitro
AZ13705339 (300 nM) prevents Siglec-8 binding-induced eosinophil death[2]. In Namalwa cells, AZ13705339 (1 μM) inhibits αIgM-controlled but not PMA-induced adhesion[3].
In vivo
In rats, AZ13705339 (100 mg/kg, p.o.) exhibits moderate clearance and Cmax of 7.7 μM[1].
AliasAZ-13705339, AZ 13705339
Chemical Properties
Molecular Weight629.75
FormulaC33H36FN7O3S
Cas No.2016806-57-6
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 225 mg/mL (357.3 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.5879 mL7.9397 mL15.8793 mL79.3966 mL
5 mM0.3176 mL1.5879 mL3.1759 mL15.8793 mL
10 mM0.1588 mL0.7940 mL1.5879 mL7.9397 mL
20 mM0.0794 mL0.3970 mL0.7940 mL3.9698 mL
50 mM0.0318 mL0.1588 mL0.3176 mL1.5879 mL
100 mM0.0159 mL0.0794 mL0.1588 mL0.7940 mL

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