Validation and invalidation of SARS-CoV-2 main protease inhibitors using the Flip-GFP and Protease-Glo luciferase assays.

SARS-CoV-2 main protease (M) is one of the most extensively exploited drug targets for COVID-19. Structurally disparate compounds have been reported as M inhibitors, raising the question of their target specificity. To elucidate the target specificity and the cellular target engagement of the claimed M inhibitors, we systematically characterize their mechanism of action using the cell-free FRET assay, the thermal shift-binding assay, the cell lysate Protease-Glo luciferase assay, and the cell-based FlipGFP assay. Collectively, our results have shown that majority of the M inhibitors identified from drug repurposing including ebselen, carmofur, disulfiram, and shikonin are promiscuous cysteine inhibitors that are not specific to M, while chloroquine, oxytetracycline, montelukast, candesartan, and dipyridamole do not inhibit M in any of the assays tested. Overall, our study highlights the need of stringent hit validation at the early stage of drug discovery.