Article
Design, synthesis, and molecular docking studies of novel pomalidomide-based PROTACs as potential anti-cancer agents targeting EGFRWT and EGFRT790M.
Journal of enzyme inhibition and medicinal chemistry - 1 Dec 2022
O Aboelez Moustafa, Belal Amany, Xiang Guangya, Ma Xiang
Abstract excerpt
A new class of EGFR PROTACs based on pomalidomide was developed, synthesised, and tested for their cytotoxic activity against a panel of human cancer cells. Compounds 15-21 were showed to be more effective against the four tested cell lines than erlotinib. In particular, compound 16 was found to be the most potent counterpart as it was 5.55, 4.34, 5.04, and 7.18 times more active than erlotinib against MCF-7,...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
