Synthesis of non-symmetric -benzylbispidinol amides and study of their inhibitory activity against the main protease of the SARS-CoV-2 virus.

Based on the data obtained by molecular modeling of the non-covalent interaction of non-symmetric -benzylbispidin-9-ol amides with the active site of the main protease 3CLpro of the SARS-CoV-2 virus, a series of compounds was synthesized, and their inhibitory activity against 3CLpro was studied and compared with that of the known inhibitor ML188 (IC = 1.56±0.55 µmol L). It was found that only compound containing the 1,4-dihydroindeno[1,2-]pyrazole fragment showed moderate activity (IC = 100±5.7µmol L) and was characterized by the highest calculated binding energy among the studied bispidine derivatives according to molecular docking data.