Identification of Promising Sulfonamide Chalcones as Inhibitors of SARS-CoV-2 3CLprothrough Structure-Based Virtual Screening and Experimental Approaches

3CLprois a viable target for developing antiviral therapies against the coronavirus. With the urgent need to find new possible inhibitors, a structure-based virtual screening approach was developed. This study recognized 75 pharmacologically bioactive compounds from our in-house library of 1052 natural product-based compounds that satisfied drug-likeness criteria and exhibited good bioavailability and membrane permeability. Among these compounds, three promising sulfonamide chalcones were identified by combined theoretical and experimental approaches, with SWC423 being the most suitable representative compound due to its competitive inhibition and low cytotoxicity in Vero E6 cells (EC50= 0.89 ± 0.32 μM; CC50= 25.54 ± 1.38 μM; SI = 28.70). The binding and stability of SWC423 in the 3CLproactive site were investigated through all-atom molecular dynamics simulation and fragment molecular orbital calculation, indicating its potential as a 3CLproinhibitor for further SARS-CoV-2 therapeutic research. These findings suggested that inhibiting 3CLprowith a sulfonamide chalcone such as SWC423 may pave the effective way for developing COVID-19 treatments.