In silico studies on phytochemicals to combat the emerging COVID-19 infection
Abdalla, Mohnad and Mohapatra, Ranjan K. and Sarangi, Ashish K. and Mohapatra, Pranab K. and Eltayb, Wafa Ali and Alam, Mahboob and El-Arabey, Amr Ahmed and Azam, Mohammad and Al-Resayes, Saud I. and Seidel, Veronique and Dhama, Kuldeep (2021) In silico studies on phytochemicals to combat the emerging COVID-19 infection. Journal of the Saudi Chemical Society, 25 (12). 101367. ISSN 1319-6103 (https://doi.org/10.1016/j.jscs.2021.101367)
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Abstract
The current COVID-19 pandemic, caused by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and its variants, remains a serious health hazard globally. The SARS-CoV-2 Mpro and spike proteins, as well as the human ACE2 receptor, have previously been reported as good targets for the development of new drug leads to combat COVID-19. Various ligands, including synthetic and plant-derived small molecules, can interact with the aforementioned proteins. In this study, we investigated the interaction of eight phytochemicals, from selected medicinal plants (Aegle marmelos, Azadirachta indica, and Ocimum sanctum) commonly used in Indian traditional medicine, with SARS-CoV-2 Mpro (PDBID: 6LU7), SARS-CoV-2S spike protein (PDB ID: 6M0J) and the human ACE2 receptor (PDB ID: 6M18). All compounds were subjected to density functional theory (DFT) and frontier molecular orbitals (FMO) analysis to determine their geometry, and key electronic and energetic properties. Upon examining the interactions of the phytochemicals with the human ACE2 receptor and the SARS-CoV-2 Mpro, spike protein targets, two compounds (C-5 and C-8) were identified as the best binding ligands. These were further examined in MD simulation studies to determine the stability of the ligand–protein interactions. QSAR, pharmacokinetic and drug-likeness properties studies revealed that C-5 may be the best candidate to serve as a template for the design and development of new drugs to combat COVID-19.
ORCID iDs
Abdalla, Mohnad, Mohapatra, Ranjan K., Sarangi, Ashish K., Mohapatra, Pranab K., Eltayb, Wafa Ali, Alam, Mahboob, El-Arabey, Amr Ahmed, Azam, Mohammad, Al-Resayes, Saud I., Seidel, Veronique ORCID: https://orcid.org/0000-0003-3880-5261 and Dhama, Kuldeep;-
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Item type: Article ID code: 78396 Dates: DateEvent31 December 2021Published19 October 2021Published Online4 October 2021AcceptedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 04 Nov 2021 14:24 Last modified: 11 Nov 2024 13:16 URI: https://strathprints.strath.ac.uk/id/eprint/78396