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孟鲁司特和替米沙坦作为严重急性呼吸综合征冠状病毒2奥密克戎变种的抑制剂。

Montelukast and Telmisartan as Inhibitors of SARS-CoV-2 Omicron Variant.

作者信息

Mulgaonkar Nirmitee, Wang Haoqi, Zhang Junrui, Roundy Christopher M, Tang Wendy, Chaki Sankar Prasad, Pauvolid-Corrêa Alex, Hamer Gabriel L, Fernando Sandun

机构信息

Biological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.

Department of Entomology, Texas A&M University, College Station, TX 77843, USA.

出版信息

Pharmaceutics. 2023 Jul 5;15(7):1891. doi: 10.3390/pharmaceutics15071891.

Abstract

Earlier studies with montelukast (M) and telmisartan (T) have revealed their potential antiviral properties against SARS-CoV-2 wild-type (WT) but have not assessed their efficacy against emerging Variants of Concern (VOCs) such as Omicron. Our research fills this gap by investigating these drugs' impact on VOCs, a topic that current scientific literature has largely overlooked. We employed computational methodologies, including molecular mechanics and machine learning tools, to identify drugs that could potentially disrupt the SARS-CoV-2 spike RBD-ACE2 protein interaction. This led to the identification of two FDA-approved small molecule drugs, M and T, conventionally used for treating asthma and hypertension, respectively. Our study presents an additional potential use for these drugs as antivirals. Our results show that both M and T can inhibit not only the WT SARS-CoV-2 but also, in the case of M, the Omicron variant, without reaching cytotoxic concentrations. This novel finding fills an existing gap in the literature and introduces the possibility of repurposing these drugs for SARS-CoV-2 VOCs, an essential step in responding to the evolving global pandemic.

摘要

早期使用孟鲁司特(M)和替米沙坦(T)的研究揭示了它们对严重急性呼吸综合征冠状病毒2型野生型(WT)的潜在抗病毒特性,但尚未评估它们对诸如奥密克戎等新出现的关注变异株(VOC)的疗效。我们的研究通过调查这些药物对VOC的影响填补了这一空白,这一主题在当前科学文献中很大程度上被忽视了。我们采用了包括分子力学和机器学习工具在内的计算方法,以识别可能破坏严重急性呼吸综合征冠状病毒2型刺突受体结合域(RBD)-血管紧张素转换酶2(ACE2)蛋白相互作用的药物。这导致识别出两种美国食品药品监督管理局(FDA)批准的小分子药物,即M和T,它们传统上分别用于治疗哮喘和高血压。我们的研究提出了这些药物作为抗病毒药物的另一种潜在用途。我们的结果表明,M和T不仅可以抑制野生型严重急性呼吸综合征冠状病毒2型,而且就M而言,还可以抑制奥密克戎变异株,且不会达到细胞毒性浓度。这一新发现填补了文献中的现有空白,并引入了将这些药物重新用于治疗严重急性呼吸综合征冠状病毒2型VOC的可能性,这是应对不断演变的全球大流行的关键一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db82/10385313/13fb3e161292/pharmaceutics-15-01891-g001.jpg

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