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Identification Of Multipotent Drugs For Covid-19 Therapeutics With The Evaluation Of Their Sars-Cov2 Inhibitory Activity

COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL(2021)

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摘要
The SARS-CoV2 is a highly contagious pathogen that causes COVID-19 disease. It has affected millions of people globally with an average lethality of similar to 3%. There is an urgent need of drugs for the treatment of COVID-19.In the current studies, we have used bioinformatics techniques to screen the FDA approved drugs against nine SARS-CoV2 proteins to identify drugs for repurposing. Additionally, we analyzed if the identified molecules can also affect the human proteins whose expression in lung changed during SARS-CoV2 infection. Targeting such genes may also be a beneficial strategy to curb disease manifestation. We have identified 74 molecules that can bind to various SARS-CoV2 and human host proteins.We experimentally validated our in-silico predictions using vero E6 cells infected with SARS-CoV2 virus. Interestingly, many of our predicted molecules viz. capreomycin, celecoxib, mefloquine, montelukast, and nebivolol showed good activity (IC50) against SARS-CoV2. We hope that these studies may help in the development of new therapeutic options for the treatment of COVID-19. (C) 2021 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
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关键词
Coronavirus, COVID-19, Drug repurposing, Network analysis, Docking, Polypharmacology, Molecular dynamics
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