Literature DB >> 12801219

Deoxyribonucleoside 2'- or 3'-mixed disulfides: prodrugs to target ribonucleotide reductase and/or to inhibit HIV reverse transcription.

Béatrice Roy1, Stéphane Chambert, Michel Lepoivre, Anne-Marie Aubertin, Jan Balzarini, Jean-Luc Décout.   

Abstract

Herein, we report the design, synthesis, and biological effects of nucleosides bearing a disulfide function on the sugar ring as prodrugs of potentially active mercaptonucleotides that can target ribonucleotide reductase or reverse transcriptase. We show that cytidine derivatives efficiently reduce dNTP pools in human CEM/SS cells and that 3'-deoxythymidin-3'-yl methyl disulfide is able to interfere with both cellular dNTP synthesis and HIV reverse transcription.

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Year:  2003        PMID: 12801219     DOI: 10.1021/jm0256225

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

1.  Synthesis of 3-fluoro-6-S-(2-S-pyridyl) nucleosides as potential lead cytostatic agents.

Authors:  Evangelia Tsoukala; Niki Tzioumaki; Stella Manta; Alexandra Riga; Jan Balzarini; Dimitri Komiotis
Journal:  Bioorg Chem       Date:  2010-08-17       Impact factor: 5.275

2.  Phosphorus-Sulfur Heterocycles Incorporating an O-P(S)-O or O-P(S)-S-S-P(S)-O Scaffold: One-Pot Synthesis and Crystal Structure Study.

Authors:  Guoxiong Hua; Kate Davidson; David B Cordes; Junyi Du; Alexandra M Z Slawin; J Derek Woollins
Journal:  Molecules       Date:  2017-10-10       Impact factor: 4.411

  2 in total

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