4.2 Article

Hemi-Babim and Fenoterol as Potential Inhibitors of MPro and Papain-like Protease against SARS-CoV-2: An In-Silico Study

期刊

MEDICINA-LITHUANIA
卷 58, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/medicina58040515

关键词

SARS-CoV-2; MPro; papain-like protease; molecular docking; molecular dynamics simulation

资金

  1. Taif University, Taif, Saudi Arabia [TURSP-2020/258]

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In this study, two drugs (Hemi-Babim and Fenoterol) were identified from the Drug Bank library that can potentially work against SARS-CoV-2. Molecular dynamics simulation studies provided evidence that these drugs can inhibit the main drug targets of the virus. Hemi-Babim and Fenoterol are repurposable drugs that have already been widely used by the public for asthma-related problems.
The coronaviruses belong to the Coronaviridae family, and one such member, severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), is causing significant destruction around the world in the form of a global pandemic. Although vaccines have been developed, their effectiveness and level of protection is still a major concern, even after emergency approval from the World Health Organisation (WHO). At the community level, no natural medicine is currently available as a cure. In this study, we screened the vast library from Drug Bank and identified Hemi-Babim and Fenoterol as agents that can work against SARS-CoV-2. Furthermore, we performed molecular dynamics (MD) simulation for both compounds with their respective proteins, providing evidence that the said drugs can work against the MPro and papain-like protease, which are the main drug targets. Inhibiting the action of these targets may lead to retaining the virus. Fenoterol is a beta-2 adrenergic agonist used for the symptomatic treatment of asthma as a bronchodilator and tocolytic. In this study, Hemi-Babim and Fenoterol showed good docking scores of -7.09 and -7.14, respectively, and performed well in molecular dynamics simulation studies. Re-purposing the above medications has huge potential, as their effects are already well-proven and under public utilisation for asthma-related problems. Hence, after the comprehensive pipeline of molecular docking, MMGBSA, and MD simulation studies, these drugs can be tested in-vivo for further human utilisation.

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