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特立氟胺:一种可能有效用于新冠病毒病综合治疗的药物。

Teriflunomide: A possible effective drug for the comprehensive treatment of COVID-19.

作者信息

Rabie Amgad M

机构信息

Dr. Amgad Rabie's Research Lab. for Drug Discovery (DARLD), Mansoura, Egypt.

Pharmaceutical Organic Chemistry Department, Faculty of Pharmacy, Mansoura University, Mansoura 35516, Egypt.

出版信息

Curr Res Pharmacol Drug Discov. 2021;2:100055. doi: 10.1016/j.crphar.2021.100055. Epub 2021 Sep 11.

DOI:10.1016/j.crphar.2021.100055
PMID:34870153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8433057/
Abstract

The coronavirus disease 2019 (COVID-19) pandemic has undoubtedly become a global crisis. Consequently, discovery and identification of new or known potential drug candidates to solve the health problems caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have become an urgent necessity. This current research study sheds light on the possible direct repurposing of the antirheumatic drug teriflunomide to act as an effective and potent anti-SARS-CoV-2 agent. Herein, an interesting computational molecular docking study of teriflunomide, to investigate and evaluate its potential inhibitory activities on the novel coronaviral-2 RNA-dependent RNA polymerase (nCoV-RdRp) protein, was reported. The docking procedures were accurately carried out on nCoV-RdRp (with/without RNA) using the COVID-19 Docking Server, through adjusting it on the small molecule docking mode. Remdesivir and its active metabolite (GS-441524) were used as the active references for the comparison and evaluation purpose. Interestingly, the computational docking analysis of the best inhibitory binding mode of teriflunomide in the binding pocket of the active site of the SARS-CoV-2 RdRp revealed that teriflunomide may exhibit significantly stronger inhibitory binding interactions and better inhibitory binding affinities (teriflunomide has considerably lower binding energies of -9.70 and -7.80 ​kcal/mol with RdRp-RNA and RdRp alone, respectively) than both references. It was previously reported that teriflunomide strongly inhibits the viral replication and reproduction through two mechanisms of action, thus the results obtained in the present study surprisingly support the double mode of antiviral action of this antirheumatic ligand. In conclusion, the current research paved the way to practically prove the hypothetical theory of the promising abilities of teriflunomide to successfully attack the SARS-CoV-2 particles and inhibit their replication in a triple mode of action through integrating the newly-discovered nCoV-RdRp-inhibiting properties with the previously-known two anticoronaviral mechanisms of action. Based on the previous interesting facts and results, the triple SARS-CoV-2/sextet COVID-19 attacker teriflunomide can further undergo / anti-COVID-19 assays together with preclinical/clinical studies and trials in an attempt to evaluate and prove its comprehensive pharmacological activities against the different SARS-CoV-2 strains to be effectively used in COVID-19 therapy in the very near future.

摘要

2019年冠状病毒病(COVID-19)大流行无疑已成为一场全球危机。因此,发现和鉴定新的或已知的潜在候选药物以解决由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的健康问题已成为当务之急。当前的这项研究揭示了抗风湿药物特立氟胺可能直接被重新用作一种有效且强效的抗SARS-CoV-2药物。在此,报道了一项关于特立氟胺的有趣的计算分子对接研究,以研究和评估其对新型冠状病毒2 RNA依赖性RNA聚合酶(nCoV-RdRp)蛋白的潜在抑制活性。对接程序通过在小分子对接模式下对COVID-19对接服务器进行调整,在nCoV-RdRp(有/无RNA)上准确进行操作。瑞德西韦及其活性代谢物(GS-441524)用作比较和评估的活性对照。有趣的是,对特立氟胺在SARS-CoV-2 RdRp活性位点结合口袋中的最佳抑制结合模式进行的计算对接分析表明,特立氟胺可能表现出比两种对照都显著更强的抑制结合相互作用和更好的抑制结合亲和力(特立氟胺与RdRp-RNA和单独的RdRp的结合能分别低得多,为-9.70和-7.80千卡/摩尔)。此前有报道称特立氟胺通过两种作用机制强烈抑制病毒复制和繁殖,因此本研究获得的结果出人意料地支持了这种抗风湿配体的双重抗病毒作用模式。总之,当前的研究为实际证明特立氟胺有望通过将新发现的nCoV-RdRp抑制特性与先前已知的两种抗冠状病毒作用机制相结合,以三重作用模式成功攻击SARS-CoV-2颗粒并抑制其复制的假设理论铺平了道路。基于先前有趣的事实和结果,三重SARS-CoV-2/六重COVID-19攻击者特立氟胺可以进一步进行抗COVID-19试验以及临床前/临床研究和试验, 试图评估和证明其针对不同SARS-CoV-2毒株的综合药理活性,以便在不久的将来有效地用于COVID-19治疗。

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