Pyrazolo[3,4-c]pyridine compounds of Formula I, including stereoisomers, geometric isomers, tautomers, and pharmaceutically acceptable salts thereof, wherein R1 and R2 are as defined herein, are useful for inhibiting Pim kinase, and for treating disorders such as cancer mediated by Pim kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
本发明提供了式I的
吡唑并[3,4-c]
吡啶化合物,包括立体异构体、几何异构体、互变异构体和其药学上可接受的盐。其中,R1和R2如本文所定义,可用于抑制Pim激酶并治疗由Pim激酶介导的癌症等疾病。本发明还公开了使用式I的化合物在哺乳动物细胞中进行体外、体内和原位诊断、预防或治疗此类疾病或相关病理状态的方法。