Synthesis and Evaluation of 5-Halo 2′,3′-Didehydro-2′,3′-Dideoxynucleosides and their Blocked Phosphoramidates as Potential Anti-Human Immunodeficiency virus Agents: An Example of ‘Kinase Bypass’
Author:
Affiliation:
1. Welsh School of Pharmacy, University of Wales Cardiff, Redwood Building, King Edward VII Avenue, Cardiff CF1 3XF, UK.
2. Rega Institute for Medical Research, Katholieke Universiteit Leuven, B-3000, Leuven, Belgium.
Publisher
SAGE Publications
Link
http://journals.sagepub.com/doi/pdf/10.1177/095632029700800605
Reference28 articles.
1. New Synthesis of 2',3'-Didehydro-2',3'-dideoxynucleosides.
2. Both 2′,3′-dideoxythymidine and its 2′,3′-unsaturated derivative (2′,3′-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro
3. Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phosphonates: potent and selective in vitro and in vivo antiretrovirus activities of (R)-9-(2-phosphonomethoxypropyl)-2,6-diaminopurine
4. Mechanism of anti-HIV action of masked alaninyl d4T-MP derivatives.
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1. Aryloxy Phosphoramidate Triesters: a Technology for Delivering Monophosphorylated Nucleosides and Sugars into Cells;ChemMedChem;2009-11-02
2. NMR conformational analysis of p-tolyl furanopyrimidine 2′-deoxyribonucleoside and crystal structure of its 3′,5′-di-O-acetyl derivative;Bioorganic & Medicinal Chemistry;2005-02
3. Phosphoramidate Protides of Carbocyclic 2′,3′‐Dideoxy‐2′,3′‐Didehydro‐7‐Deazaadenosine with Potent Activity Against HIV and HBV;Nucleosides, Nucleotides and Nucleic Acids;2004-01-12
4. NOVEL ARYL SUBSTITUTED BICYCLIC FURO NUCLEOSIDES AS EXTREMELY POTENT AND SELECTIVE ANTI-VZV AGENTS;Nucleosides, Nucleotides and Nucleic Acids;2001-03-31
5. Fluorescent bicyclic furo pyrimidine deoxynucleoside analogs as potent and selective inhibitors of VZV and potential future drugs for the treatment of chickenpox and shingles;Drugs of the Future;2000
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