Evidence map›Paper›PMID 37514075›Full record

ArticlePharmaceutics2023

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

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

Abstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Nirmitee MulgaonkarBiological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0003-4607-8391
Haoqi WangBiological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.
Junrui ZhangBiological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.
Christopher M RoundyDepartment of Entomology, Texas A&M University, College Station, TX 77843, USA.
Wendy TangDepartment of Entomology, Texas A&M University, College Station, TX 77843, USA.
Sankar Prasad ChakiTexas A&M Global Health Research Complex, Division of Research, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0002-8130-6997
Alex Pauvolid-CorrêaDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0002-6924-157X
Gabriel L HamerDepartment of Entomology, Texas A&M University, College Station, TX 77843, USA.
Sandun FernandoBiological and Agricultural Engineering Department, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0002-7692-2170

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

antiviralCOVID-19drug repurposingmontelukastSARS-CoV-2

Identifiers

PMID37514075
PMCPMC10385313

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.