Identification of a Quinolone-Based Scaffold as a Dual SARS-COV-2 PLᵖʳᵒ and Mᵖʳᵒ Inhibitor: An Integrated Molecular Modeling and In-vitro Evaluation Approach

Introduction: The papain-like protease (PLᵖʳᵒ) plays a critical role in the SARS-CoV-2 life cycle by regulating both viral replication and immune evasion, making it an attractive target for antiviral drug development. Methods: In this study, a virtual screening strategy combining pharmacophore modeling, molecular docking, enzymatic evaluation, and molecular dynamics (MD) simulations was employed to identify novel PLᵖʳᵒ inhibitors. From this process, 30 top ranked candidates were selected for experimental enzymatic evaluation. Results: of 124.8 µM against PLᵖʳᵒ. Molecular dynamics simulations of 100 ns revealed that the lead compound forms a stable complex with PLᵖʳᵒ, exhibiting interaction patterns comparable to those of the co-crystallized ligand. Furthermore, MM-GB/SA binding free energies were calculated from the MD trajectories for the lead (ST50940260), the derivative (Z30231927), and the co-crystallized ligand in 7JN2. The lead demonstrated favourable binding (-27.33 kcal/mol) within a comparable range, while the derivative showed the most favourable binding (-30.26 kcal/mol), followed closely by the co-crystallized reference (-29.82 kcal/mol). Conclusion: Overall, these findings highlight ST50940260 as a promising lead candidate for further optimization, with potential dual inhibitory activity against both proteases.