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发明授权
CN1701073B 作为细胞周期蛋白依赖激酶抑制剂的吡唑并[1,5-A]嘧啶 失效 - 权利终止

作为细胞周期蛋白依赖激酶抑制剂的吡唑并[1,5-A]嘧啶
摘要：
在本发明的许多实施方案中，提供了新类型的作为细胞周期蛋白依赖激酶抑制剂的吡唑并[1，5-a]嘧啶化合物、这类化合物的制备方法、包括一种或多种这类化合物的药物组合物、包括一种或多种这类化合物的药物制剂的制备方法，以及用这类化合物或药物组合物治疗、预防、抑制或改善一种或多种与CDK有关的疾病的方法。
摘要（英）：

In its many embodiments, the present invention provides a novel class of pyrazolo[1,5-a]pyrimidine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions.

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