Bisphosphonate inhibitors of ATP-mediated HIV-1 reverse transcriptase catalyzed excision of chain-terminating 3'-azido, 3'-deoxythymidine: a QSAR investigation

Bioorg Med Chem. 2008 Oct 1;16(19):8959-67. doi: 10.1016/j.bmc.2008.08.047. Epub 2008 Aug 27.

Abstract

We report the results of an investigation of the inhibition of the ATP-mediated HIV-1 reverse transcriptase catalyzed phosphorolysis in vitro of AZT from AZT-terminated DNA primers by a series of 42 bisphosphonates. The four most active compounds possess neutral, halogen-substituted phenyl or biphenyl sidechains and have IC(50) values < 1 microM in excision inhibition assays. Use of two comparative molecular similarity analysis methods to analyze these inhibition results yielded a classification model with an overall accuracy of 94%, and a regression model having good accord with experiment (q(2)=0.63, r(2)=0.91), with the experimental activities being predicted within, on average, a factor of 2. The most active species had little or no toxicity against three human cell lines (IC(50)(avg) > 200 microM). These results are of general interest since they suggest that it may be possible to develop potent bisphosphonate-based AZT-excision inhibitors with little cellular toxicity, opening up a new route to restoring AZT sensitivity in otherwise resistant HIV-1 strains.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Anti-HIV Agents / chemistry
  • Anti-HIV Agents / pharmacology*
  • Catalysis
  • Cell Line, Tumor
  • DNA Primers / metabolism
  • Dideoxynucleotides / chemistry
  • Dideoxynucleotides / metabolism*
  • Diphosphonates / antagonists & inhibitors*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • HIV Reverse Transcriptase / antagonists & inhibitors*
  • Halogens / chemistry
  • Halogens / metabolism
  • Humans
  • Inhibitory Concentration 50
  • Phosphoric Acids / chemistry
  • Phosphoric Acids / metabolism
  • Quantitative Structure-Activity Relationship*
  • Regression Analysis
  • Thymine Nucleotides / chemistry
  • Thymine Nucleotides / metabolism*
  • Zidovudine / analogs & derivatives*
  • Zidovudine / chemistry
  • Zidovudine / metabolism

Substances

  • Anti-HIV Agents
  • DNA Primers
  • Dideoxynucleotides
  • Diphosphonates
  • Enzyme Inhibitors
  • Halogens
  • Phosphoric Acids
  • Thymine Nucleotides
  • 3'-azido-3'-deoxythymidine 5'phosphate
  • Zidovudine
  • Adenosine Triphosphate
  • HIV Reverse Transcriptase