Disclosed are the ERK inhibitors of formula 1.0:
and the pharmaceutically acceptable salts, esters and solvates thereof. Q is a piperidine or piperazine ring that can have a bridge or a fused ring. The piperidine ring can have a double bond in the ring. All other substitutents are as defined herein. Also disclosed are methods of treating cancer using the compounds of formula 1.0.
本发明公开了式1.0的ERK
抑制剂及其药学上可接受的盐、
酯和溶剂化物。其中,Q是一个带有桥或融合环的
哌啶或
哌嗪环。
哌啶环中可以在环上具有双键。所有其他取代基如本文所定义。本发明还公开了使用式1.0的化合物治疗癌症的方法。