Discovery of potent small molecule PROTACs targeting mutant EGFR
Hongyi Zhao(Xi'an Jiaotong University), San‐Qi Zhang(Xi'an Jiaotong University), Minhang Xin(Xi'an Jiaotong University), Xiao-Xiao Xi(Xi'an Jiaotong University), Xueyan Yang(Xi'an Jiaotong University), Junjie Zhang(Chemical Synthesis Lab), Hao Lei(Xi'an Jiaotong University), Shemin Lu(Xi'an Jiaotong University)
Cited by 94
Related Papers
Small molecule selenium-containing compounds: Recent development and therapeutic applications
|European Journal of Medicinal Chemistry|2021|233
Review of the molecular mechanisms of Ganoderma lucidum triterpenoids: Ganoderic acids A, C2, D, F, DM, X and Y
|European Journal of Medicinal Chemistry|2019|192
The development of Bruton's tyrosine kinase (BTK) inhibitors from 2012 to 2017: A mini-review
|European Journal of Medicinal Chemistry|2018|168
Discovery of potent epidermal growth factor receptor (EGFR) degraders by proteolysis targeting chimera (PROTAC)
|European Journal of Medicinal Chemistry|2020|120
Strategies to target the Hedgehog signaling pathway for cancer therapy
|Medicinal Research Reviews|2018|108