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Title: Potential drugs for the treatment of AIDS
Authors: De Clercq, Erik # ×
Issue Date: Jan-1989
Publisher: Oxford University Press
Series Title: The Journal of Antimicrobial Chemotherapy vol:23 Suppl A pages:35-46
Abstract: From our investigations the following compounds have emerged as particularly potent and selective inhibitors of HIV replication: sulphated polysaccharides (i.e. heparin, dextran sulphate, pentosan polysulphate), dideoxynucleoside analogues such as the 3'-azido-and 3'-fluoro-substituted 2',3'-dideoxyribosides of both purines (i.e. guanine, 2,6-diaminopurine) and pyrimidines (i.e. uracil, thymine), and the 9-(2-phosphonylmethoxyethyl) derivatives of adenine, 2-monoaminopurine and 2,6-diaminopurine. All these compounds yield great promise for the treatment of retrovirus infections in humans. Whereas the sulphated polysaccharides interfere with the virus adsorption process, the nucleoside analogues (following intracellular phosphorylation to their 5'-triphosphate) appear to be targeted at the reverse transcriptase.
URI: 
ISSN: 0305-7453
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Virology and Chemotherapy (Rega Institute)
× corresponding author
# (joint) last author

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