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FRAX1036

FRAX1036

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商品描述
FRAX1036,HY-19538,MCE:
Description

FRAX1036 is a PAK inhibitor with Kis of 23.3 nM, 72.4 nM, and 2.4 μM for PAK1, PAK2 and PAK4, respectively.

IC50 & Target

PAK1

23.3 nM (Ki)

PAK2

72.4 nM (Ki)

PAK4

2.4 μM (Ki)

In Vitro

FRAX1036 is a PAK inhibitor with Kis of 23.3 nM, 72.4 nM, and 2.4 μM for PAK1, PAK2 and PAK4, respectively. FRAX1036 (2.5 μM) incombination with docetaxel alters stathmin phosphorylation, induces the apoptotic marker cleaved PARP and increases kinetics of apoptosis in MDA-MB-175 and HCC2911 cells; also alters microtubule organization, mitosis and cell fate in U2OS cells. Moreover, FRAX1036 shows significantly effective inhibition on U2OS cells. FRAX1036 (10 μM) affects the proliferation of non-small cell lung cancer (NSCLC) cells when added to KRAS prenylation inhibitors.

Solvent & Solubility
In Vitro: 

DMSO : 5.3 mg/mL (10.23 mM; Need warming)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.9303 mL 9.6516 mL 19.3032 mL
5 mM 0.3861 mL 1.9303 mL 3.8606 mL
10 mM 0.1930 mL 0.9652 mL 1.9303 mL
*Please refer to the solubility information to select the appropriate solvent.



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