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Inhibitory Potential of Chromene Derivatives on Structural and Non-Structural Proteins of Dengue Virus
Dengue fever is a mosquito-borne viral disease that has become a serious health issue across the globe. It is caused by a virus of the Flaviviridae family, and it comprises five different serotypes (DENV-1 to DENV-5). As there is no specific medicine or effective vaccine for controlling dengue fever...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787897/ https://www.ncbi.nlm.nih.gov/pubmed/36560664 http://dx.doi.org/10.3390/v14122656 |
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author | Dharmapalan, Babitha Thekkiniyedath Biswas, Raja Sankaran, Sathianarayanan Venkidasamy, Baskar Thiruvengadam, Muthu George, Ginson Rebezov, Maksim Zengin, Gokhan Gallo, Monica Montesano, Domenico Naviglio, Daniele Shariati, Mohammad Ali |
author_facet | Dharmapalan, Babitha Thekkiniyedath Biswas, Raja Sankaran, Sathianarayanan Venkidasamy, Baskar Thiruvengadam, Muthu George, Ginson Rebezov, Maksim Zengin, Gokhan Gallo, Monica Montesano, Domenico Naviglio, Daniele Shariati, Mohammad Ali |
author_sort | Dharmapalan, Babitha Thekkiniyedath |
collection | PubMed |
description | Dengue fever is a mosquito-borne viral disease that has become a serious health issue across the globe. It is caused by a virus of the Flaviviridae family, and it comprises five different serotypes (DENV-1 to DENV-5). As there is no specific medicine or effective vaccine for controlling dengue fever, there is an urgent need to develop potential inhibitors against it. Traditionally, various natural products have been used to manage dengue fever and its co-morbid conditions. A detailed analysis of these plants revealed the presence of various chromene derivatives as the major phytochemicals. Inspired by these observations, authors have critically analyzed the anti-dengue virus potential of various 4H chromene derivatives. Further, in silico, in vitro, and in vivo reports of these scaffolds against the dengue virus are detailed in the present manuscript. These analogues exerted their activity by interfering with various stages of viral entry, assembly, and replications. Moreover, these analogues mainly target envelope protein, NS2B-NS3 protease, and NS5 RNA-dependent RNA polymerase, etc. Overall, chromene-containing analogues exerted a potent activity against the dengue virus and the present review will be helpful for the further exploration of these scaffolds for the development of novel antiviral drug candidates. |
format | Online Article Text |
id | pubmed-9787897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97878972022-12-24 Inhibitory Potential of Chromene Derivatives on Structural and Non-Structural Proteins of Dengue Virus Dharmapalan, Babitha Thekkiniyedath Biswas, Raja Sankaran, Sathianarayanan Venkidasamy, Baskar Thiruvengadam, Muthu George, Ginson Rebezov, Maksim Zengin, Gokhan Gallo, Monica Montesano, Domenico Naviglio, Daniele Shariati, Mohammad Ali Viruses Review Dengue fever is a mosquito-borne viral disease that has become a serious health issue across the globe. It is caused by a virus of the Flaviviridae family, and it comprises five different serotypes (DENV-1 to DENV-5). As there is no specific medicine or effective vaccine for controlling dengue fever, there is an urgent need to develop potential inhibitors against it. Traditionally, various natural products have been used to manage dengue fever and its co-morbid conditions. A detailed analysis of these plants revealed the presence of various chromene derivatives as the major phytochemicals. Inspired by these observations, authors have critically analyzed the anti-dengue virus potential of various 4H chromene derivatives. Further, in silico, in vitro, and in vivo reports of these scaffolds against the dengue virus are detailed in the present manuscript. These analogues exerted their activity by interfering with various stages of viral entry, assembly, and replications. Moreover, these analogues mainly target envelope protein, NS2B-NS3 protease, and NS5 RNA-dependent RNA polymerase, etc. Overall, chromene-containing analogues exerted a potent activity against the dengue virus and the present review will be helpful for the further exploration of these scaffolds for the development of novel antiviral drug candidates. MDPI 2022-11-28 /pmc/articles/PMC9787897/ /pubmed/36560664 http://dx.doi.org/10.3390/v14122656 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Dharmapalan, Babitha Thekkiniyedath Biswas, Raja Sankaran, Sathianarayanan Venkidasamy, Baskar Thiruvengadam, Muthu George, Ginson Rebezov, Maksim Zengin, Gokhan Gallo, Monica Montesano, Domenico Naviglio, Daniele Shariati, Mohammad Ali Inhibitory Potential of Chromene Derivatives on Structural and Non-Structural Proteins of Dengue Virus |
title | Inhibitory Potential of Chromene Derivatives on Structural and Non-Structural Proteins of Dengue Virus |
title_full | Inhibitory Potential of Chromene Derivatives on Structural and Non-Structural Proteins of Dengue Virus |
title_fullStr | Inhibitory Potential of Chromene Derivatives on Structural and Non-Structural Proteins of Dengue Virus |
title_full_unstemmed | Inhibitory Potential of Chromene Derivatives on Structural and Non-Structural Proteins of Dengue Virus |
title_short | Inhibitory Potential of Chromene Derivatives on Structural and Non-Structural Proteins of Dengue Virus |
title_sort | inhibitory potential of chromene derivatives on structural and non-structural proteins of dengue virus |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787897/ https://www.ncbi.nlm.nih.gov/pubmed/36560664 http://dx.doi.org/10.3390/v14122656 |
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