Structural basis for the potential antitumour activity of DNA-interacting benzo[kl]xanthene lignans

Org Biomol Chem. 2011 Feb 7;9(3):701-10. doi: 10.1039/c0ob00480d. Epub 2010 Nov 16.

Abstract

The biological properties and possible pharmacological applications of benzo[kl]xanthene lignans, rare among natural products and synthetic compounds, are almost unexplored. In the present contribution, the possible interaction of six synthetic benzo[kl]xanthene lignans and the natural metabolite rufescidride with DNA has been investigated through a combined STD-NMR and molecular docking approach, paralleled by in vitro biological assays on their antiproliferative activity towards two different cancer cell lines: SW 480 and HepG2. Our data suggest that the benzo[kl]xanthene lignans are suitable lead compounds for the design of DNA selective ligands with potential antitumour properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antinematodal Agents / chemistry*
  • Antinematodal Agents / pharmacology
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • DNA / chemistry*
  • Humans
  • Inhibitory Concentration 50
  • Lignans / chemistry*
  • Lignans / pharmacology
  • Models, Molecular
  • Nucleic Acid Conformation*
  • Structure-Activity Relationship
  • Xanthenes / chemistry*
  • Xanthenes / pharmacology

Substances

  • Antinematodal Agents
  • Lignans
  • Xanthenes
  • DNA