Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 2: Identification and optimisation of substituted 2,4-bis anilino pyrimidines

Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 2: Identification and optimisation of substituted 2,4-bis anilino pyrimidines
复制标题

DOI:
10.1016/s0960-894x(03)00203-8
复制
发表时间:
2003-09-15
影响因子:
2.7
通讯作者:
Pease, JE
Pease, JE
中科院分区:
医学4区
文献类型:
--
作者:
Breault, GA;Ellston, RPA;Pease, JE

文献摘要

被引文献

相似文献

通过化学修饰和X-射线结晶学分析,我们确定了2,4-双苯胺基嘧啶类化合物为CDK4的有效抑制剂。在这里,我们描述了这个系列的优化。(C)2003爱思唯尔有限公司。保留所有权利。
Through chemical modification and X-ray crystallography we identified the 2,4-bis anilino pyrimidines as potent inhibitors of CDK4. Herein, we describe the optimisation of this series. (C) 2003 Elsevier Ltd. All rights reserved.