化学
变构调节
磷酸化
蛋白质水解
MEK抑制剂
细胞生物学
药理学
生物化学
MAPK/ERK通路
酶
生物
作者
Stefan Vollmer,Danen Cunoosamy,Huafei Lv,Huanxi Feng,Xia Li,Ziyang Nan,Wenzhen Yang,Matthew W. D. Perry
标识
DOI:10.1021/acs.jmedchem.9b00810
摘要
PROteolysis TArgeting Chimeras (PROTACs) targeting the degradation of MEK have been designed based on allosteric MEK inhibitors. Inhibition of the phosphorylation of ERK1/2 was less effective with the PROTACs than a small-molecule inhibitor; the best PROTACs, however, were more effective in inhibiting proliferation of A375 cells than an inhibitor.
科研通智能强力驱动
Strongly Powered by AbleSci AI