[CAS NO. 1224887-10-8]  GSK2256098

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PRODUCTS SPECIFICATIONS [1224887-10-8]

Store
Catalog
SLK-S8523
Brand
Selleck
CAS
1224887-10-8

DESCRIPTION [1224887-10-8]

Overview

MDLMFCD30502650
Molecular Weight414.89
Molecular FormulaC20H23ClN6O2
SMILESO=C(NOC)C1=CC=CC=C1NC2=CC(NC3=CC(C)=NN3C(C)C)=NC=C2Cl

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM2.4103 mL12.0514 mL24.1028 mL
5 mM0.4821 mL2.4103 mL4.8206 mL
10 mM0.2410 mL1.2051 mL2.4103 mL
50 mM0.0482 mL0.2410 mL0.4821 mL

Description

GSK2256098 is a potent, selective, reversible, and ATP competitive inhibitor with apparent Ki of 0.4 nM. GSK2256098 inhibits cancer cell growth and induces .

Targets

FAK [5]
0.4 nM(Ki)

In vitro

GSK2256098 has been developed to inhibit FAK activity through targeting the phosphorylation site of FAK, tyrosine (Y) 397. After a 30-min incubation, GSK2256098 inhibits FAK activity or Y397 phosphorylation in cancer cell lines, OVCAR8 (ovary), U87MG (brain), and A549 (lung), at IC50 values of 15, 8.5 and 12 nM, respectively. In addition, the data suggests that cellular inhibition of FAK by GSK2256098 can occur as early as 30 min in cultured cells and lasts up to 12 hours in mouse tumor xenografts. GSK2256098 inhibition of FAK kinase activity can decrease Akt and ERK activity. PI3K/Akt and ERK signaling contributes to cell survival, implying a pharmacological value of GSK2256098 in attenuation of abnormal survival pathways in specific types of PDAC cells. GSK2256098 can promote apoptosis in L3.6P1 cells through caspase-9/PARP-related pathways. It attenuates abnormal growth and aberrant motility of PDAC cells in a FAK specific manner.GSK2256098 also inhibits growth, migration, and invasion and induces apoptosis in a subset of GBM cell lines.