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Montelukast and Telmisartan as Inhibitors of SARS-CoV-2 Omicron Variant.
Mulgaonkar, Nirmitee; Wang, Haoqi; Zhang, Junrui; Roundy, Christopher M; Tang, Wendy; Chaki, Sankar Prasad; Pauvolid-Corrêa, Alex; Hamer, Gabriel L; Fernando, Sandun.
Afiliação
  • Mulgaonkar N; Biological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.
  • Wang H; Biological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.
  • Zhang J; Biological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.
  • Roundy CM; Department of Entomology, Texas A&M University, College Station, TX 77843, USA.
  • Tang W; Department of Entomology, Texas A&M University, College Station, TX 77843, USA.
  • Chaki SP; Texas A&M Global Health Research Complex, Division of Research, Texas A&M University, College Station, TX 77843, USA.
  • Pauvolid-Corrêa A; Department of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX 77843, USA.
  • Hamer GL; Department of Entomology, Texas A&M University, College Station, TX 77843, USA.
  • Fernando S; Biological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.
Pharmaceutics ; 15(7)2023 Jul 05.
Article em En | MEDLINE | ID: mdl-37514075
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Pharmaceutics Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Pharmaceutics Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos