Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 1: identification and optimisation of substituted 4,6-Bis anilino pyrimidines
作者:John F. Beattie、Gloria A. Breault、Rebecca P.A. Ellston、Stephen Green、Philip J. Jewsbury、Catherine J. Midgley、Russell T. Naven、Claire A. Minshull、Richard A. Pauptit、Julie A. Tucker、J.Elizabeth Pease
DOI:10.1016/s0960-894x(03)00202-6
日期:2003.9
Using a high-throughput screening campaign, we identified the 4,6-bis anilino pyrimidines as inhibitors of the cyclin-dependent kinase, CDK4. Herein we describe the further chemical modification and use of X-ray crystallography to develop potent and selective in vitro inhibitors of CDK4.
使用高通量筛选活动,我们确定了4,6-bis苯胺嘧啶为细胞周期蛋白依赖性激酶CDK4的抑制剂。在这里,我们描述了进一步的化学修饰和X射线晶体学的用途,以开发有效和选择性的CDK4体外抑制剂。