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Therapeutic potential of coumarins as antiviral agents

Coumarins have received a considerable attention in the last three decades as a lead structures for the discovery of orally bioavailable non-peptidic antiviral agents. A lot of structurally diverse coumarins analogues were found to display remarkable array of affinity with the different molecular ta...

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Detalles Bibliográficos
Autores principales: Hassan, Mohd. Zaheen, Osman, Hasnah, Ali, Mohamed Ashraf, Ahsan, Mohamed Jawed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Masson SAS. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115672/
https://www.ncbi.nlm.nih.gov/pubmed/27484512
http://dx.doi.org/10.1016/j.ejmech.2016.07.056
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author Hassan, Mohd. Zaheen
Osman, Hasnah
Ali, Mohamed Ashraf
Ahsan, Mohamed Jawed
author_facet Hassan, Mohd. Zaheen
Osman, Hasnah
Ali, Mohamed Ashraf
Ahsan, Mohamed Jawed
author_sort Hassan, Mohd. Zaheen
collection PubMed
description Coumarins have received a considerable attention in the last three decades as a lead structures for the discovery of orally bioavailable non-peptidic antiviral agents. A lot of structurally diverse coumarins analogues were found to display remarkable array of affinity with the different molecular targets for antiviral agents and slight modifications around the central motif result in pronounced changes in its antiviral spectrum. This manuscript thoroughly reviews the design, discovery and structure–activity relationship studies of the coumarin analogues as antiviral agents focusing mainly on lead optimization and its development into clinical candidates.
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spelling pubmed-71156722020-04-02 Therapeutic potential of coumarins as antiviral agents Hassan, Mohd. Zaheen Osman, Hasnah Ali, Mohamed Ashraf Ahsan, Mohamed Jawed Eur J Med Chem Article Coumarins have received a considerable attention in the last three decades as a lead structures for the discovery of orally bioavailable non-peptidic antiviral agents. A lot of structurally diverse coumarins analogues were found to display remarkable array of affinity with the different molecular targets for antiviral agents and slight modifications around the central motif result in pronounced changes in its antiviral spectrum. This manuscript thoroughly reviews the design, discovery and structure–activity relationship studies of the coumarin analogues as antiviral agents focusing mainly on lead optimization and its development into clinical candidates. Elsevier Masson SAS. 2016-11-10 2016-07-25 /pmc/articles/PMC7115672/ /pubmed/27484512 http://dx.doi.org/10.1016/j.ejmech.2016.07.056 Text en © 2016 Elsevier Masson SAS. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Hassan, Mohd. Zaheen
Osman, Hasnah
Ali, Mohamed Ashraf
Ahsan, Mohamed Jawed
Therapeutic potential of coumarins as antiviral agents
title Therapeutic potential of coumarins as antiviral agents
title_full Therapeutic potential of coumarins as antiviral agents
title_fullStr Therapeutic potential of coumarins as antiviral agents
title_full_unstemmed Therapeutic potential of coumarins as antiviral agents
title_short Therapeutic potential of coumarins as antiviral agents
title_sort therapeutic potential of coumarins as antiviral agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115672/
https://www.ncbi.nlm.nih.gov/pubmed/27484512
http://dx.doi.org/10.1016/j.ejmech.2016.07.056
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