Heterocycle amino alkyloxy substituted quinazoline derivatives as represented by the structural Formula (I) and pharmaceutically acceptable salts thereof, capable of inhibiting the activity of receptor tyrosine kinase EGFR, and being used to treat cancers related to the expression of the receptor tyrosine kinase of the ErbB family are provided.
本发明提供了异环
氨基烷
氧基取代的
喹唑啉衍
生物,其结构式表示为(I),以及其药学上可接受的盐,能够抑制受体
酪氨酸激酶
EGFR的活性,并用于治疗与ErbB家族受体
酪氨酸激酶表达相关的癌症。