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Selective inhibitors of clinically important variants of EGFR tyrosine kinase

机译:EGFR酪氨酸激酶临床上重要变异体的选择性抑制剂

摘要

The present invention relates to compounds of the formula (I) or a subgeneric structure or species thereof, or pharmaceutically acceptable salts, esters, solvates and / or prodrugs thereof and abnormal cell growth such as cancer Provide methods and compositions for treating or ameliorating sexual disorders, wherein A, R 2 , R 3 , R 10 , E 1 , E 2 , E 3 , Y, and Z are defined herein As it is. The compounds and salts of the invention inhibit kinases, in particular epidermal growth factor receptor EGFR, and certain variants thereof that are important in developing resistance to treatment with EGFR inhibition therapy, such as cancer, etc. Useful for treating or ameliorating aberrant cell proliferative disorders. 【Selection chart】 None
机译:本发明涉及式(I)的化合物或其亚类结构或种类,或其药学上可接受的盐,酯,溶剂化物和/或前药以及异常细胞生长,例如癌症,提供治疗或改善性障碍的方法和组合物,其中A,R 2 ,R 3 ,R 10 ,E 1 ,E 2 < / Sup>,E 3 ,Y和Z此处按原样定义。本发明的化合物和盐抑制激酶,特别是表皮生长因子受体EGFR,及其某些变异体,这些激酶在发展对EGFR抑制疗法的治疗例如癌症等的抵抗力中很重要。 。 【选型表】无

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