Alkylated piperazine compounds of Formula I are provided, including stereoisomers, tautomers, and pharmaceutically acceptable salts thereof, useful for inhibiting Btk kinase, and for treating cancer mediated by Btk kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, and treatment of cancer in mammalian cells, or associated pathological conditions, are disclosed.
提供了式I的烷基化
哌嗪化合物,包括立体异构体,互变异构体和其药学上可接受的盐,用于抑制Btk激酶并治疗由Btk激酶介导的癌症。公开了使用式I的化合物进行哺乳动物细胞中癌症的体外,体内和原位诊断和治疗,或相关病理条件的方法。