cycloSal-Pronucleotides of 2‘-Fluoro-ara- and 2‘-Fluoro-ribo-2‘,3‘- dideoxyadenosine as a Strategy to Bypass a Metabolic Blockade

Author:

Meier Chris1,Knispel Tina1,Marquez Victor E.1,Siddiqui Maqbool A.1,De Clercq Erik1,Balzarini Jan1

Affiliation:

1. Institute of Organic Chemistry, Julius-Maximilians-University Würzburg, Am Hubland, D-97074 Würzburg, Germany, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4255, and Rega Institute for Medical Research, Katholieke Universiteit Leuven, B-3000 Leuven, Belgium

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Reference52 articles.

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2. Metabolism and mechanism of antiretroviral action of purine and pyrimidine derivatives

3. (b) Herdewijn, P.; Balzarini, J.; De Clercq, E. 2‘,3‘-Dideoxynucleoside Analogues as Anti-HIV Agents. InAdvances in Antiviral Drug Design; De Clercq, E., Ed.; JAI Press Inc.  Greenwich, London, 1993; Vol. 1, pp 233−318.

4. Didanosine

5. Didanosine

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