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Nucleosides and emerging viruses: A new story

With several US Food and Drug Administration (FDA)-approved drugs and high barriers to resistance, nucleoside and nucleotide analogs remain the cornerstone of antiviral therapies for not only herpesviruses, but also HIV and hepatitis viruses (B and C); however, with the exception of severe acute res...

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Detalles Bibliográficos
Autores principales: Roy, Vincent, Agrofoglio, Luigi A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8856764/
https://www.ncbi.nlm.nih.gov/pubmed/35189369
http://dx.doi.org/10.1016/j.drudis.2022.02.013
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author Roy, Vincent
Agrofoglio, Luigi A.
author_facet Roy, Vincent
Agrofoglio, Luigi A.
author_sort Roy, Vincent
collection PubMed
description With several US Food and Drug Administration (FDA)-approved drugs and high barriers to resistance, nucleoside and nucleotide analogs remain the cornerstone of antiviral therapies for not only herpesviruses, but also HIV and hepatitis viruses (B and C); however, with the exception of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), for which vaccines have been developed at unprecedented speed, there are no vaccines or small antivirals yet available for (re)emerging viruses, which are primarily RNA viruses. Thus, herein, we present an overview of ribonucleoside analogs recently developed and acting as inhibitors of the viral RNA-dependent RNA polymerase (RdRp). They are new lead structures that will be exploited for the discovery of new antiviral nucleosides.
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spelling pubmed-88567642022-02-22 Nucleosides and emerging viruses: A new story Roy, Vincent Agrofoglio, Luigi A. Drug Discov Today Post-Screen (Grey) With several US Food and Drug Administration (FDA)-approved drugs and high barriers to resistance, nucleoside and nucleotide analogs remain the cornerstone of antiviral therapies for not only herpesviruses, but also HIV and hepatitis viruses (B and C); however, with the exception of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), for which vaccines have been developed at unprecedented speed, there are no vaccines or small antivirals yet available for (re)emerging viruses, which are primarily RNA viruses. Thus, herein, we present an overview of ribonucleoside analogs recently developed and acting as inhibitors of the viral RNA-dependent RNA polymerase (RdRp). They are new lead structures that will be exploited for the discovery of new antiviral nucleosides. Elsevier Ltd. 2022-07 2022-02-19 /pmc/articles/PMC8856764/ /pubmed/35189369 http://dx.doi.org/10.1016/j.drudis.2022.02.013 Text en © 2022 Elsevier Ltd. 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 Post-Screen (Grey)
Roy, Vincent
Agrofoglio, Luigi A.
Nucleosides and emerging viruses: A new story
title Nucleosides and emerging viruses: A new story
title_full Nucleosides and emerging viruses: A new story
title_fullStr Nucleosides and emerging viruses: A new story
title_full_unstemmed Nucleosides and emerging viruses: A new story
title_short Nucleosides and emerging viruses: A new story
title_sort nucleosides and emerging viruses: a new story
topic Post-Screen (Grey)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8856764/
https://www.ncbi.nlm.nih.gov/pubmed/35189369
http://dx.doi.org/10.1016/j.drudis.2022.02.013
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