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Synthesis and biological activity of aza and deaza analogues of purine nucleosides

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Anastasiya L'vovna Khandazhinskaya 1
Anastasiya L'vovna Khandazhinskaya
1 Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow
10.1070/RCR5013
Published 30 November 2020
Review , RCR5013, Volume 90, Issue 11, 1454-1491
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Matyugina E. S., Kochetkov S. N., Khandazhinskaya A. L. Synthesis and biological activity of aza and deaza analogues of purine nucleosides // Russian Chemical Reviews. 2020. Vol. 90. No. 11. pp. 1454-1491.
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Matyugina E. S., Kochetkov S. N., Khandazhinskaya A. L. Synthesis and biological activity of aza and deaza analogues of purine nucleosides // Russian Chemical Reviews. 2020. Vol. 90. No. 11. pp. 1454-1491.
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TY - JOUR
DO - 10.1070/RCR5013
UR - https://rcr.colab.ws/publications/10.1070/RCR5013
TI - Synthesis and biological activity of aza and deaza analogues of purine nucleosides
T2 - Russian Chemical Reviews
AU - Matyugina, Elena Sergeevna
AU - Kochetkov, Sergei Nikolaevich
AU - Khandazhinskaya, Anastasiya L'vovna
PY - 2020
DA - 2020/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 1454-1491
IS - 11
VL - 90
ER -
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@article{2020_Matyugina,
author = {Elena Sergeevna Matyugina and Sergei Nikolaevich Kochetkov and Anastasiya L'vovna Khandazhinskaya},
title = {Synthesis and biological activity of aza and deaza analogues of purine nucleosides},
journal = {Russian Chemical Reviews},
year = {2020},
volume = {90},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RCR5013},
number = {11},
pages = {1454--1491},
doi = {10.1070/RCR5013}
}
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Matyugina, Elena Sergeevna, et al. “Synthesis and biological activity of aza and deaza analogues of purine nucleosides.” Russian Chemical Reviews, vol. 90, no. 11, Nov. 2020, pp. 1454-1491. https://rcr.colab.ws/publications/10.1070/RCR5013.
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Keywords

aza/deaza purine nucleosides
biological activity
carbohydrate fragment
heterocyclic base

Abstract

Analogues and derivatives of nucleic acid components have been used as key drugs in different areas of medicine over the past decades. The replacement of one or more nitrogen atoms of the heterocyclic base with a CH group affords deazapurine nucleoside analogues, and the replacement of the methine group with a nitrogen atom gives azapurine derivatives. A combination of aza and deaza moieties in the purine base leads to aza(deaza)-modified bases. Some nucleoside analogues were found to exhibit pronounced anticancer and antiviral activity. The synthesis and evaluation of biological activity of aza- and deazapurine nucleoside analogues have attracted interest from researchers four decades ago. This review describes and integrates the studies concerning certain aspects of the synthesis and(or) activity of various representatives of this class of compounds. The structure--biological activity relationships are analyzed. The successful approaches to the design of aza- and deazapurine nucleoside analogues are considered. A comparison is given for the methods of chemical and enzymatic synthesis of these compounds.

The bibliography includes 161 references.

Funders

Russian Science Foundation
19-74-10048

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