A cell-permeable pyrrolo-pyrazine compound that acts as a potent, selective, reversible, and ATP-competitive inhibitor of cyclin dependent kinases (Cdks: IC50 =150nM, 120 nM, 400 nM and 200 nM for Cdk1/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E, and Cdk5/p25,
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参考文献
• Mitsuhashi, M., et al.: Pharm. Res., 25, 1116 (2003)
• Mattey, Y., et al.: J. Med. Chem., 46, 222 (2003)
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