Synthesis and anti-HIV-1 integrase activity of modified dinucleotides

Eur J Med Chem. 2009 Dec;44(12):5029-44. doi: 10.1016/j.ejmech.2009.09.007. Epub 2009 Sep 9.

Abstract

The synthesis of a series of thirty-eight new modified dinucleotides and dinucleotide conjugate analogues of d-(5')ApC(3') is described. The inhibitory activity of these compounds toward HIV-1 integrase was examined in enzymatic assays using the natural dinucleotide as a reference. Among the compounds, a perylene-dinucleotide conjugate has shown a two micromolar anti-integrase activity due to the presence of both the intercalator and the dinucleotide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Assay
  • Dinucleoside Phosphates* / chemical synthesis
  • Dinucleoside Phosphates* / chemistry
  • Dinucleoside Phosphates* / pharmacology
  • HIV Integrase Inhibitors* / chemical synthesis
  • HIV Integrase Inhibitors* / pharmacology
  • HIV-1 / drug effects*
  • Humans
  • Molecular Structure
  • Perylene* / chemistry

Substances

  • Dinucleoside Phosphates
  • HIV Integrase Inhibitors
  • Perylene