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Useful diaminothiazoles as selective inhibitors of CDK4

机译:有用的二氨基噻唑类化合物作为CDK4的选择性抑制剂

摘要

The present invention is directed to novel diaminothiazoles of formulaThese compounds inhibit cyclin-dependent kinase 4 (Cdk4) and are selective against Cdk2 and Cdk1. These compounds and their pharmaceutically acceptable salts and esters have antiproliferative activity and are useful in the treatment or control of cancer, in particular solid tumors. This invention is also directed to pharmaceutical compositions containing such compounds and to methods of treating or controlling cancer, most particularly the treatment or control of breast, lung and colon and prostate tumors.
机译:本发明涉及下式的新型二氨基噻唑:这些化合物抑制细胞周期蛋白依赖性激酶4(Cdk4)并对Cdk2和Cdk1具有选择性。这些化合物及其药学上可接受的盐和酯具有抗增殖活性,可用于治疗或控制癌症,特别是实体瘤。本发明还涉及含有这类化合物的药物组合物,以及治疗或控制癌症的方法,最特别地是治疗或控制乳腺癌,肺癌,结肠癌和前列腺癌。

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