Virtual screening and molecular simulation study of natural products database for lead identification of novel coronavirus main protease inhibitors. Issue 8 (24th May 2022)

• Record Type: Journal Article
• Authors: Tripathi, Nancy; Goel, Bharat; Bhardwaj, Nivedita; Sahu, Bharat; Kumar, Hemant; Jain, Shreyans K.
• Is Part Of: Journal of biomolecular structure & dynamics. Volume 40:Issue 8(2022)
• Page Start: 3655
• Page End: 3667
• Publication Date: 2022-05-24
• Subjects: COVID-19 -- natural products -- virtual screening -- molecular docking -- protease inhibitors; Biomolecules -- Periodicals; Molecular structure -- Periodicals; Molecular Biology -- Periodicals; Biomechanics -- Periodicals; 572
• DOI: 10.1080/07391102.2020.1848630
• Languages: English
• ISSNs: 0739-1102

Abstract

Abstract: 3CL like protease (3CLpro or Mpro) is one of the main proteases of 2019-nCoV. The 3CLpro is a nonstructural protein of SARS-CoV and has an essential role in viral replication and transcription, thus, could be a potential target for anti-SARS drug development. The present study employed ligand- and structure-based approaches to identify the potent inhibitors of 2019-nCoV protease. The e-pharmacophore developed from 3CLpro-1 yielded virtual hits, that were subjected through drug likeliness and PAINS filters to remove interfering compounds. Further comprehensive docking studies, free energy calculations and ADMET studies resulted in two virtual leads- MolPort-000-410-348 and MolPort-002-530-156. The compounds MolPort-000-410-348 and MolPort-002-530-156 displayed good docking score of −12.09 and −13.38 Kcal/mol and free binding energy of −63.34 ± 2.03 and −61.52 ± 2.24 Kcal/mol, respectively. The compounds also exhibited satisfactory predicted ADMET profile and were subjected to molecular dynamic (MD) studies. The MD simulation produced stable complexes of these ligands with 3CLpro protein and ligand RMSD in acceptable limits. Communicated by Ramaswamy H. Sarma