» Articles » PMID: 35566073

Drug Repurposing for COVID-19: A Review and a Novel Strategy to Identify New Targets and Potential Drug Candidates

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2022 May 14
PMID 35566073
Authors
Affiliations
Soon will be listed here.
Abstract

In December 2019, the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 (COVID-19) was first identified in the province of Wuhan, China. Since then, there have been over 400 million confirmed cases and 5.8 million deaths by COVID-19 reported worldwide. The urgent need for therapies against SARS-CoV-2 led researchers to use drug repurposing approaches. This strategy allows the reduction in risks, time, and costs associated with drug development. In many cases, a repurposed drug can enter directly to preclinical testing and clinical trials, thus accelerating the whole drug discovery process. In this work, we will give a general overview of the main developments in COVID-19 treatment, focusing on the contribution of the drug repurposing paradigm to find effective drugs against this disease. Finally, we will present our findings using a new drug repurposing strategy that identified 11 compounds that may be potentially effective against COVID-19. To our knowledge, seven of these drugs have never been tested against SARS-CoV-2 and are potential candidates for in vitro and in vivo studies to evaluate their effectiveness in COVID-19 treatment.

Citing Articles

Diverse Applications of the Anti-Diabetic Drug Metformin in Treating Human Disease.

Roberts C, Raabe N, Wiegand L, Kadar Shahib A, Rastegar M Pharmaceuticals (Basel). 2025; 17(12.

PMID: 39770443 PMC: 11677501. DOI: 10.3390/ph17121601.


AI Promoted Virtual Screening, Structure-Based Hit Optimization, and Synthesis of Novel COVID-19 S-RBD Domain Inhibitors.

Gkekas I, Katsamakas S, Mylonas S, Fotopoulou T, Magoulas G, Tenchiu A J Chem Inf Model. 2024; 64(22):8562-8585.

PMID: 39535926 PMC: 11600510. DOI: 10.1021/acs.jcim.4c01110.


Characterization of the symmetrical benzimidazole twin drug TL1228: the role as viral entry inhibitor for fighting COVID-19.

Murdocca M, Andrade Santos-Filho O, De Masi C, Dos Santos Rodrigues E, Campos de Souza C, De Santis R Biol Direct. 2024; 19(1):93.

PMID: 39415197 PMC: 11481581. DOI: 10.1186/s13062-024-00523-9.


Evaluation of Drug and Herbal Medicinal Promotions on Social Media During the COVID-19 Pandemic in Relation to World Health Organization Ethical Criteria and South African Health Products Regulatory Authority Guidelines in South Africa:....

Chimukuche R, Ndlazi J, Mtolo L, Bird K, Seeley J Online J Public Health Inform. 2024; 16:e58378.

PMID: 39293046 PMC: 11447434. DOI: 10.2196/58378.


Repurposed Drugs during the Outbreak of Pandemic COVID-19: A Mini-Review on Their Molecular Structures and Hit-and-Trial Results.

Devi T, Devi M, Okram M, Singh O ACS Omega. 2024; 9(35):36858-36864.

PMID: 39246499 PMC: 11375728. DOI: 10.1021/acsomega.4c05357.


References
1.
Bojkova D, Bechtel M, McLaughlin K, McGreig J, Klann K, Bellinghausen C . Aprotinin Inhibits SARS-CoV-2 Replication. Cells. 2020; 9(11). PMC: 7692688. DOI: 10.3390/cells9112377. View

2.
Sakai Y, Kawachi K, Terada Y, Omori H, Matsuura Y, Kamitani W . Two-amino acids change in the nsp4 of SARS coronavirus abolishes viral replication. Virology. 2017; 510:165-174. PMC: 7111695. DOI: 10.1016/j.virol.2017.07.019. View

3.
Humbert M, de Blay F, Garcia G, Prudhomme A, Leroyer C, Magnan A . Masitinib, a c-kit/PDGF receptor tyrosine kinase inhibitor, improves disease control in severe corticosteroid-dependent asthmatics. Allergy. 2009; 64(8):1194-201. DOI: 10.1111/j.1398-9995.2009.02122.x. View

4.
Rahman M, Hoque M, Islam M, Islam I, Mishu I, Rahaman M . Mutational insights into the envelope protein of SARS-CoV-2. Gene Rep. 2020; 22:100997. PMC: 7723457. DOI: 10.1016/j.genrep.2020.100997. View

5.
Neves B, Braga R, Bezerra J, Cravo P, Andrade C . In silico repositioning-chemogenomics strategy identifies new drugs with potential activity against multiple life stages of Schistosoma mansoni. PLoS Negl Trop Dis. 2015; 9(1):e3435. PMC: 4287566. DOI: 10.1371/journal.pntd.0003435. View