| Literature DB >> 12801219 |
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.Entities:
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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