Enzymatically Activated cycloSal-d4T-monophosphates: The Third Generation of cycloSal-Pronucleotides-Reference-Cited by-同舟云学术

Enzymatically Activated cycloSal-d4T-monophosphates: The Third Generation of cycloSal-Pronucleotides

Published:2007-03-03 Issue:7 Volume:50 Page:1658-1667
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Gisch Nicolas¹,Balzarini Jan¹,Meier Chris¹

Affiliation:

1. Department of Chemistry, Organic Chemistry, Faculty of Sciences, University of Hamburg, Martin-Luther-King-Platz 6, 20146 Hamburg, Germany, and Rega-Institute for Medical Research, Katholieke Universiteit Leuven, Minderbroedersstraat 10, 3000 Leuven, Belgium

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm0613267

Reference27 articles.

1. Strategies in the design of antiviral drugs

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

3. 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. Pronucleotides: Toward thein vivo delivery of antiviral and anticancer nucleotides

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