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Deoxyribonucleoside 2'- or 3'-mixed disulfides: prodrugs to target ribonucleotide reductase and/or to inhibit HIV reverse transcription.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2003 Jun 19; Vol. 46 (13), pp. 2565-8. - Publication Year :
- 2003
-
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.
- Subjects :
- Animals
Anti-HIV Agents chemistry
Anti-HIV Agents pharmacology
Cell Division drug effects
Cells, Cultured
Deoxyribonucleosides chemistry
Deoxyribonucleosides pharmacology
Disulfides chemistry
Disulfides pharmacology
HIV-1 drug effects
HIV-2 drug effects
Humans
Mice
Prodrugs chemistry
Prodrugs pharmacology
Reverse Transcriptase Inhibitors chemistry
Reverse Transcriptase Inhibitors pharmacology
Stavudine analogs & derivatives
Stavudine chemistry
Stavudine pharmacology
Structure-Activity Relationship
T-Lymphocytes cytology
T-Lymphocytes drug effects
Anti-HIV Agents chemical synthesis
Deoxyribonucleosides chemical synthesis
Disulfides chemical synthesis
Prodrugs chemical synthesis
Reverse Transcriptase Inhibitors chemical synthesis
Ribonucleotide Reductases antagonists & inhibitors
Stavudine chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 0022-2623
- Volume :
- 46
- Issue :
- 13
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12801219
- Full Text :
- https://doi.org/10.1021/jm0256225