化学
喹唑啉
激酶
药理学
体内
突变体
阿法替尼
MAPK/ERK通路
蛋白激酶B
PI3K/AKT/mTOR通路
立体化学
癌症研究
生物化学
磷酸化
埃罗替尼
信号转导
受体
生物
表皮生长因子受体
基因
生物技术
作者
Leifu Yang,Yaxin Li,Yunling Du,Yan Guo,Zhenke Guo,Baoxiu Liu,Jianglin Liu,Yanfei Liu,Hongdan Niu,Yueming Sun,Henglin Yan,Yajuan Yang,Shannan Yu,Yifan Zhang,Yuan Zhang,Kun Zheng,Nanqiao Zheng,Xiaoqing Zhang,Qiang Zhang,Liming Hu
标识
DOI:10.1021/acs.jmedchem.3c02302
摘要
HER2 mutations were seen in 4% of non-small-cell lung cancer (NSCLC) patients. Most of these mutations (90%) occur as an insertion mutation within the exon 20 frame, leading to the downstream activation of the PI3K-AKT and RAS/MAPK pathways. However, no targeted therapies have yet been approved worldwide. Here a novel series of highly potent HER2 inhibitors with a pyrido[2,3,4-
科研通智能强力驱动
Strongly Powered by AbleSci AI