Structure-based Drug Design, ADME and Molecular Docking analyses of anti-viral agents against SARS-CoV-2 virus, Zika virus and Hepatitis C virus

Authors

Abstract

Computer-aided drug design has been taking an increasing role in the field of modern drug discovery.  These in silico computational methods are cost-effective, reduce the use of animal models in pharmacological research, and can be used to study pathogenic organisms without the need for any facilities. Based on the structure of known anti-viral agents, a total of 812 ligands have been designed. All ligands were screened for drug-likeness based on Lipinski rule of five. A database of ligands was constructed and in silico docking analyses were performed using MOE 2015.10 program against three selected viruses, viz., Zika virus, Hepatitis C virus and SARS-CoV-2 virus. Ligand 93 (-8.4469 kcal/mol) and ligand 123 (-8.3609 kcal/mol) were identified to be having higher docking scores as compared to the native ligand 6T8 (-8.2839 kcal/mol) and could be considered potential candidates for further studies in anti-viral drugs against Zika virus. Ligands 153 (-10.3108 kcal/mol), 63 (-9.9968 kcal/mol), 621 (-9.8700 kcal/mol), 31 (-9.5001 kcal/mol) and 779 (-9.3874 kcal/com) were identified as the top five binding ligands, and have docking scores much higher than the reference native ligand K4J (-8.9037 kcal/com). All these ligands can be potent candidates for anti-viral research against Hepatitis C virus. Ligand 798 (-8.0957 kcal/com) and ligand 63 (-8.0778 kcal/com) have higher docking scores as compared to the reference native ligand X77 (-8.0689 kcal/mol), they also interact with the catalytic dyad at the active site of the target protein and can be considered as possible candidates for studies in anti-viral drugs against SARS-CoV-2.

Keywords: Computer-aided drug design, ADME, Molecular Docking analyses, anti-viral agents, Sars-CoV-2 virus, Zika virus, Hepatitis C virus

Keywords:

Computer-aided drug design, ADME, Molecular Docking analyses, anti-viral agents, Sars-CoV-2 virus, Zika virus, Hepatitis C virus

DOI

https://doi.org/10.22270/jddt.v13i7.5909

Author Biographies

Peter Solo, Department of Chemistry, St. Joseph’s College autonomous, Jakhama, Nagaland, India.

Department of Chemistry, St. Joseph’s College autonomous, Jakhama, Nagaland, India.

Sangdintuile Zeliang, Department of Chemistry, St. Joseph’s College autonomous, Jakhama, Nagaland, India.

Department of Chemistry, St. Joseph’s College autonomous, Jakhama, Nagaland, India.

Muluvelu Lohe, Department of Chemistry, St. Joseph’s College autonomous, Jakhama, Nagaland, India.

Department of Chemistry, St. Joseph’s College autonomous, Jakhama, Nagaland, India.

Avünü Neikha, Department of Chemistry, St. Joseph’s College autonomous, Jakhama, Nagaland, India.

Department of Chemistry, St. Joseph’s College autonomous, Jakhama, Nagaland, India.

Akumsunep Jamir, Department of Evnironmental Studies, St. Xavier’s College, Jalukie, Nagaland, India.

Department of Evnironmental Studies, St. Xavier’s College, Jalukie, Nagaland, India.

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Published

2023-07-15
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How to Cite

1.
Solo P, Zeliang S, Lohe M, Neikha A, Jamir A. Structure-based Drug Design, ADME and Molecular Docking analyses of anti-viral agents against SARS-CoV-2 virus, Zika virus and Hepatitis C virus. J. Drug Delivery Ther. [Internet]. 2023 Jul. 15 [cited 2026 Feb. 2];13(7):65-74. Available from: https://www.jddtonline.info/index.php/jddt/article/view/5909

How to Cite

1.
Solo P, Zeliang S, Lohe M, Neikha A, Jamir A. Structure-based Drug Design, ADME and Molecular Docking analyses of anti-viral agents against SARS-CoV-2 virus, Zika virus and Hepatitis C virus. J. Drug Delivery Ther. [Internet]. 2023 Jul. 15 [cited 2026 Feb. 2];13(7):65-74. Available from: https://www.jddtonline.info/index.php/jddt/article/view/5909