Heterocyclic pyrimidine compounds that modulate mutant-selective epidermal growth factor receptor (EGFR) and ALK kinase activity are disclosed. More specifically, the invention provides pyrimidines which inhibit, regulate and/or modulate kinase receptor, particularly in selectively modulation of various EGFR mutant activity and ALK kinase activity have been disclosed. Pharmaceutical compositions comprising the pyrimidine derivative, and methods of treatment for diseases associated with protein kinase enzymatic activity, particularly EGFR or ALK kinase activity including non-small cell lung cancer comprising administration of the pyrimidine derivative are disclosed.
                            本发明公开了能调节突变选择性
表皮生长因子受体(
EGFR)和 ALK 激酶活性的杂环
嘧啶化合物。更具体地说,本发明提供了抑制、调节和/或调节激酶受体的
嘧啶类化合物,特别是选择性调节各种
表皮生长因子受体突变体活性和 ALK 激酶活性的
嘧啶类化合物。本发明公开了包含
嘧啶衍
生物的药物组合物,以及通过服用
嘧啶衍
生物治疗与蛋白激酶酶活性有关的疾病,特别是
表皮生长因子受体或ALK激酶活性,包括非小细胞肺癌的方法。