维兰特罗与布地奈德对SARS-CoV-2 Mpro潜在抑制活性的分子动力学模拟方法

Afzal Hussain, A. Hussain
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引用次数: 0

摘要

一种新型人类冠状病毒,即严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的快速和广泛传播,突出表明迫切需要确定一种潜在的药物来对抗COVID-19感染。在这封信中,我们调查了药物再利用作为一种有吸引力的技术,可以通过重新利用现有药物来治疗疾病,而不是最初的适应症,从而帮助药物开发。采用GROMACS (200ns)进行维兰特罗与布地奈德对COVID-19 Mpro的分子动力学(MD)模拟。结果表明,RMSD、RMSF、旋转半径和氢键分析更倾向于维兰特罗而不是布地奈德。最终需要动物实验和可靠的临床试验来确定这些药物的潜在预防和治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Finding the potential inhibitory activity of Vilanterol Versus Budesonide towards SARS-CoV-2 Mpro: A molecular dynamics simulation approach
The fast and widespread spread of a novel human coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), highlights the urgent need to identify a potential drug to combat COVID-19 infection. In this letter, we investigated drug repurposing as an appealing technique that can help with drug development by repurposing existing drugs to treat illnesses apart from their initial indications. The molecular dynamics (MD) simulations using GROMACS (200ns) were carried out for Vilanterol Versus Budesonide towards COVID-19 Mpro. The results indicated that the RMSD, RMSF, Radius of gyration, and Hydrogen-bond analysis favored Vilanterol over Budesonide. Animal investigations and reliable clinical trials will eventually be required to establish the potential preventive and therapeutic effects of these drugs.
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