Abstract
Anti-HIV drugs act by blocking intracellular replication of the virus by inhibiting viral enzyme either reverse transcriptase or protease. Reverse transcriptase inhibitors belong to 3 different categories: nucleoside analogues, which active forms are the triphosphorylated intracellular compound, non nucleoside inhibitors and the more recent nucleotide analogues. Protease inhibitors are very active in vitro but besides their digestive side effects, have numerous drug interactions because they are metabolised through P450 liver cytochromes, and are associated with long-term toxicity.
MeSH terms
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Anti-HIV Agents / adverse effects
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Anti-HIV Agents / classification
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Anti-HIV Agents / pharmacology
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Anti-HIV Agents / therapeutic use*
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Cytochrome P-450 Enzyme System / drug effects
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Drug Interactions
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HIV / drug effects
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HIV / enzymology
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HIV Protease Inhibitors / adverse effects
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HIV Protease Inhibitors / pharmacology
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HIV Protease Inhibitors / therapeutic use
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Humans
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Liver / drug effects
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Liver / enzymology
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Reverse Transcriptase Inhibitors / classification
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Reverse Transcriptase Inhibitors / pharmacology
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Reverse Transcriptase Inhibitors / therapeutic use
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Virus Replication / drug effects
Substances
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Anti-HIV Agents
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HIV Protease Inhibitors
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Reverse Transcriptase Inhibitors
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Cytochrome P-450 Enzyme System