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2000
Volume 10, Issue 18
  • ISSN: 0929-8673
  • E-ISSN: 1875-533X

Abstract

A review is presented on different categories of compounds that have been studied for the inhibition of the HIV-1 integrase to develop anti-HIV agents. These compounds are: oligonucleotides (double-stranded, triplex, and G-quartet), curcumin analogues, polyhydroxylated aromatic compounds, diketo acids, caffeoyl- and galloyl - based compounds, hydrazides and amides, tetracyclines, and depsides and depsidones. For all these compounds, the important structural features essential for the inhibition of the integrase are pointed out.

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/content/journals/cmc/10.2174/0929867033456972
2003-09-01
2025-05-19
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  • Article Type:
    Review Article
Keyword(s): double-stranded; hiv-1 integrase; integrase inhibitors; oligonucleotides
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