Inhibition of HIV-1 replication in cultured cells with phosphorylated dideoxyuridine derivatives encapsulated in immunoliposomes

Author:

Zelphati Olivier,Degols Geneviève,Loughrey Helen,Leserman Lee,Pompon Alain,Puech Frédéric,Maggio Annie-Françoise,Imbach Jean-Louis,Gosselin Gilles

Publisher

Elsevier BV

Subject

Virology,Pharmacology

Reference39 articles.

1. Both 2′,3′-dideoxythymidine and its 2′,3′-unsaturated derivative (2′,3′-dideoxythimidinene) are potent and selective inhibitors of Human Immunodeficiency Virus replication in vitro;Baba;Biochem. Biophys. Res. Commun.,1987

2. Anti-retrovirus activity of 3′-fluoro- and 3′-azido-substituted pyrimidine 2′,3′-dideoxynucleoside analogues;Balzarini;Biochem. Pharmacol.,1988

3. The anti-HTLVIII(anti-HIV) and cytotoxic activity of 2′,3′-didehydro-2′,3′-dideoxyribonucleosides: a comparison with their parental 2′,3′-dideoxyribonucleosides;Balzarini;Mol. Pharmacol.,1987

4. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immunodeficiency syndrome (AIDS);Barré-Sinoussi;Science,1983

5. On the therapeutic use of nucleosides and the penetrability of phosphorylated compounds;Cohen;Biochem. Pharmacol.,1975

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