tcsc0881 CVT-313

CVT-313 is a potent, selective, reversible, and ATP-competitive inhibitor of CDK2 with IC₅₀ of 0.5 μM.

IC50 & Target: IC50: 0.5 μM (CDK2), 4.2 μM (CDK1), 215 μM (CDK4)^[1]

In Vitro: CVT-313 has been shown to inhibit other kinases, but at much higher IC₅₀ values, i.e., CDK1 (IC₅₀=4.2 μM), CDK4 D1 (IC₅₀=215 μM), and MAPK/PKA/PKC (IC₅₀>1.25 mM), compared to CDK2 (IC₅₀=0.5 μM). CVT-313 has been shown to have profound effects on cell proliferation at concentrations of 5-20 μM^[1]. CVT-313 is a potent CDK2 inhibitor, which is identified from a purine analog library with an IC₅₀ of 0.5 μM in vitro. Inhibition is competitive with respect to ATP (K_i=95 nM), and selective CVT-313 has no effect on other, nonrelated ATP-dependent serine/threonine kinases. When added to CDK1 or CDK4, a 8.5- and 430-fold higher concentration of CVT-313 is required for half-maximal inhibition of the enzyme activity. Using normal and tumor human/murine cell lines, the effects of CVT-313 on cell proliferation is measured. The IC₅₀ for growth inhibition ranged from 1.25 to 20 μM^[2].