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

Author:

Mulgaonkar Nirmitee1ORCID,Wang Haoqi1,Zhang Junrui1,Roundy Christopher M.2,Tang Wendy2,Chaki Sankar Prasad3ORCID,Pauvolid-Corrêa Alex4ORCID,Hamer Gabriel L.2,Fernando Sandun1ORCID

Affiliation:

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

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

3. Texas A&M Global Health Research Complex, Division of Research, Texas A&M University, College Station, TX 77843, USA

4. Department of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX 77843, USA

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.

Funder

Texas A&M AgriLife Research Insect Vector Diseases Grant Program

Publisher

MDPI AG

Subject

Pharmaceutical Science

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