Phenylsulfonamide substituted, pyrazolo[1,5-a]pyrimidines are described. The compounds of the invention selectively inhibit Raf kinase activity and are useful for treating disorders associated with Raf kinases. Formula (I)
苯磺酰胺取代的
吡唑并[1,5-a]
嘧啶已被描述。该发明的化合物选择性地抑制Raf激酶活性,并可用于治疗与Raf激酶相关的疾病。公式(I)