Aryl H-Phosphonates 18. Synthesis, properties, and biological activity of 2',3'-dideoxynucleoside (N-heteroaryl)phosphoramidates of increased lipophilicity

Eur J Med Chem. 2015 Jul 15:100:77-88. doi: 10.1016/j.ejmech.2015.06.004. Epub 2015 Jun 4.

Abstract

Recently, AZT (N-pyridyl)phosphoramidates were reported as a new type of potential anti-HIV therapeutics. In continuation of that work, here we present new (N-heteroaryl)phosphoramidate derivatives of antiviral 2',3'-dideoxynucleosides containing other types of N-heteroaryl moieties, particularly those with higher lipophilicity. The present studies comprise mechanistic investigations using (31)P NMR correlation analysis, which permitted improvements in the synthetic procedures. The obtained compounds were tested in biological systems to establish their cytotoxicity and anti-HIV activity. The results were analyzed with respect to possible correlations between biological and physico-chemical properties of the phosphoramidates studied, to get some insight into their antiviral mode of action.

Keywords: 2′,3′-dideoxynucleosides; AZT; Anti-HIV; H-phosphonates; Heteroaryl amines; Lipophilicity; Phosphoramidates; Pro-nucleotides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-HIV Agents / chemical synthesis
  • Anti-HIV Agents / chemistry
  • Anti-HIV Agents / pharmacology*
  • Cell Line
  • Cell Survival
  • Dideoxynucleosides / chemical synthesis
  • Dideoxynucleosides / chemistry
  • Dideoxynucleosides / pharmacology*
  • Dose-Response Relationship, Drug
  • HIV-1 / drug effects
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Structure-Activity Relationship

Substances

  • Anti-HIV Agents
  • Dideoxynucleosides