Design and synthesis of isatin derivatives as effective SARS-CoV-2 3CL protease inhibitors
Description
SARS-CoV-2 chymotrypsin-like cysteine protease (3CL^(pro) ) is one of the most widely developed drug targets for COVID-19. This study aimed to design and synthesize isatin derivatives to target SARS-CoV-2 3CL^(pro) in a covalent binding manner
