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Antiviral nucleoside analogs

[Image: see text] The minireview surveys the modification of native nucleosides as a result of which huge libraries of nucleoside analogs of various structures were synthesized. Particular attention is paid to the synthesis of the so-called prodrug forms of nucleoside analogs which ensure their pene...

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Detalles Bibliográficos
Autores principales: Kataev, Vladimir E., Garifullin, Bulat F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8118684/
https://www.ncbi.nlm.nih.gov/pubmed/34007086
http://dx.doi.org/10.1007/s10593-021-02912-8
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author Kataev, Vladimir E.
Garifullin, Bulat F.
author_facet Kataev, Vladimir E.
Garifullin, Bulat F.
author_sort Kataev, Vladimir E.
collection PubMed
description [Image: see text] The minireview surveys the modification of native nucleosides as a result of which huge libraries of nucleoside analogs of various structures were synthesized. Particular attention is paid to the synthesis of the so-called prodrug forms of nucleoside analogs which ensure their penetration into the cell and metabolism to active 5'-triphosphate derivatives. All the best known antiviral cyclic nucleoside analogs approved for the treatment of HIV infections, hepatitis B, C, and influenza since the 1960s, as well as those in various stages of clinical trials in recent years, are listed. Nucleoside analogs that have shown the ability to inhibit the replication of SARS-CoV and MERS-CoV are discussed, including remdesivir, approved by the FDA for emergency use in the fight against COVID-19.
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spelling pubmed-81186842021-05-14 Antiviral nucleoside analogs Kataev, Vladimir E. Garifullin, Bulat F. Chem Heterocycl Compd (N Y) Reviews [Image: see text] The minireview surveys the modification of native nucleosides as a result of which huge libraries of nucleoside analogs of various structures were synthesized. Particular attention is paid to the synthesis of the so-called prodrug forms of nucleoside analogs which ensure their penetration into the cell and metabolism to active 5'-triphosphate derivatives. All the best known antiviral cyclic nucleoside analogs approved for the treatment of HIV infections, hepatitis B, C, and influenza since the 1960s, as well as those in various stages of clinical trials in recent years, are listed. Nucleoside analogs that have shown the ability to inhibit the replication of SARS-CoV and MERS-CoV are discussed, including remdesivir, approved by the FDA for emergency use in the fight against COVID-19. Springer US 2021-05-14 2021 /pmc/articles/PMC8118684/ /pubmed/34007086 http://dx.doi.org/10.1007/s10593-021-02912-8 Text en © Springer Science+Business Media, LLC, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Reviews
Kataev, Vladimir E.
Garifullin, Bulat F.
Antiviral nucleoside analogs
title Antiviral nucleoside analogs
title_full Antiviral nucleoside analogs
title_fullStr Antiviral nucleoside analogs
title_full_unstemmed Antiviral nucleoside analogs
title_short Antiviral nucleoside analogs
title_sort antiviral nucleoside analogs
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8118684/
https://www.ncbi.nlm.nih.gov/pubmed/34007086
http://dx.doi.org/10.1007/s10593-021-02912-8
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