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Nucleoside Analogs with Fleximer Nucleobase
[Image: see text] This review article is devoted to the so-called fleximer nucleoside analogs, containing two or more planar moieties in the heterocyclic base, connected by a bond that permits rotation. Such analogs have been proposed as molecular probes for detecting enzyme–substrate interactions a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364132/ https://www.ncbi.nlm.nih.gov/pubmed/32836313 http://dx.doi.org/10.1007/s10593-020-02713-5 |
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author | Chudinov, Mikhail V. |
author_facet | Chudinov, Mikhail V. |
author_sort | Chudinov, Mikhail V. |
collection | PubMed |
description | [Image: see text] This review article is devoted to the so-called fleximer nucleoside analogs, containing two or more planar moieties in the heterocyclic base, connected by a bond that permits rotation. Such analogs have been proposed as molecular probes for detecting enzyme–substrate interactions and studying the transcription and translation of nucleic acids, but subsequently have attracted the interest of researchers by their antiviral and antitumor activity. The methods used in the synthesis of such compounds, along with their structural features and also biological activity are considered in this review. |
format | Online Article Text |
id | pubmed-7364132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-73641322020-07-16 Nucleoside Analogs with Fleximer Nucleobase Chudinov, Mikhail V. Chem Heterocycl Compd (N Y) Article [Image: see text] This review article is devoted to the so-called fleximer nucleoside analogs, containing two or more planar moieties in the heterocyclic base, connected by a bond that permits rotation. Such analogs have been proposed as molecular probes for detecting enzyme–substrate interactions and studying the transcription and translation of nucleic acids, but subsequently have attracted the interest of researchers by their antiviral and antitumor activity. The methods used in the synthesis of such compounds, along with their structural features and also biological activity are considered in this review. Springer US 2020-07-16 2020 /pmc/articles/PMC7364132/ /pubmed/32836313 http://dx.doi.org/10.1007/s10593-020-02713-5 Text en © Springer Science+Business Media, LLC, part of Springer Nature 2020 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 | Article Chudinov, Mikhail V. Nucleoside Analogs with Fleximer Nucleobase |
title | Nucleoside Analogs with Fleximer Nucleobase |
title_full | Nucleoside Analogs with Fleximer Nucleobase |
title_fullStr | Nucleoside Analogs with Fleximer Nucleobase |
title_full_unstemmed | Nucleoside Analogs with Fleximer Nucleobase |
title_short | Nucleoside Analogs with Fleximer Nucleobase |
title_sort | nucleoside analogs with fleximer nucleobase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364132/ https://www.ncbi.nlm.nih.gov/pubmed/32836313 http://dx.doi.org/10.1007/s10593-020-02713-5 |
work_keys_str_mv | AT chudinovmikhailv nucleosideanalogswithfleximernucleobase |