Literature DB >> 27086793

Cytokinin Nucleosides - Natural Compounds with a Unique Spectrum of Biological Activities.

Mikhail S Drenichev, Vladimir E Oslovsky, Sergey N Mikhailov1.   

Abstract

Cytokinin nucleosides exhibit antitumor, antiviral, antiprotozoal, blood pressure reducing, anti-inflammatory, and antipsychotic activity. These compounds also influence platelet aggregation and exhibit some other biological activities. Cytokinins are N6-substituted adenines and represent an important group of phytohormones with diverse biochemical functions in plants, stimulating cell division and plant growth. The main structural feature of cytokinin nucleosides is the presence of a hydrophobic hydrocarbon moiety at the N6-position of adenosine. This moiety is responsible for a difference in physicochemical and biological properties as compared to adenosine. 1-N-Tuberculosinyladenosine and N6-tuberculosinyladenosine are specifically produced by Mycobacterium tuberculosis as components of the plasmatic membrane, thus making them attractive targets for clinical test development. Structurally related compounds were found in marine organisms. It has been shown also that tRNA contains N6-isoprenyladenosine and some other related compounds. This review summarizes the structural features, biological activity, and the synthesis of cytokinin nucleosides and some of their closely related derivatives such as cytokinins and terpene derivatives of adenine.

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Year:  2016        PMID: 27086793     DOI: 10.2174/1568026616666160414123717

Source DB:  PubMed          Journal:  Curr Top Med Chem        ISSN: 1568-0266            Impact factor:   3.295


  5 in total

1.  In Vitro and In Silico Studies of Human Tyrosyl-DNA Phosphodiesterase 1 (Tdp1) Inhibition by Stereoisomeric Forms of Lipophilic Nucleosides: The Role of Carbohydrate Stereochemistry in Ligand-Enzyme Interactions.

Authors:  Nadezhda S Dyrkheeva; Irina A Chernyshova; Georgy A Ivanov; Yuri B Porozov; Anastasia A Zenchenko; Vladimir E Oslovsky; Alexandra L Zakharenko; Darina I Nasyrova; Galina N Likhatskaya; Sergey N Mikhailov; Olga I Lavrik; Mikhail S Drenichev
Journal:  Molecules       Date:  2022-04-09       Impact factor: 4.927

2.  Anion exchange resins in phosphate form as versatile carriers for the reactions catalyzed by nucleoside phosphorylases.

Authors:  Julia N Artsemyeva; Ekaterina A Remeeva; Tatiana N Buravskaya; Irina D Konstantinova; Roman S Esipov; Anatoly I Miroshnikov; Natalia M Litvinko; Igor A Mikhailopulo
Journal:  Beilstein J Org Chem       Date:  2020-10-22       Impact factor: 2.883

3.  Comparative Analysis of Enzymatic Transglycosylation Using E. coli Nucleoside Phosphorylases: A Synthetic Concept for the Preparation of Purine Modified 2'-Deoxyribonucleosides from Ribonucleosides.

Authors:  Mikhail S Drenichev; Vladimir E Oslovsky; Anastasia A Zenchenko; Claudia V Danilova; Mikhail A Varga; Roman S Esipov; Dmitry D Lykoshin; Cyril S Alexeev
Journal:  Int J Mol Sci       Date:  2022-03-03       Impact factor: 5.923

4.  Fluorination of Naturally Occurring N⁶-Benzyladenosine Remarkably Increased Its Antiviral Activity and Selectivity.

Authors:  Vladimir E Oslovsky; Mikhail S Drenichev; Liang Sun; Nikolay N Kurochkin; Vladislav E Kunetsky; Carmen Mirabelli; Johan Neyts; Pieter Leyssen; Sergey N Mikhailov
Journal:  Molecules       Date:  2017-07-20       Impact factor: 4.411

5.  Antiviral and Antimicrobial Nucleoside Derivatives: Structural Features and Mechanisms of Action.

Authors:  A A Zenchenko; M S Drenichev; I A Il'icheva; S N Mikhailov
Journal:  Mol Biol       Date:  2021-12-17       Impact factor: 1.374

  5 in total

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