Synthesis and biological evaluation of 2-(3',4',5'-trimethoxybenzoyl)-3-N,N-dimethylamino benzo[b]furan derivatives as inhibitors of tubulin polymerization

Bioorg Med Chem. 2008 Sep 15;16(18):8419-26. doi: 10.1016/j.bmc.2008.08.029. Epub 2008 Aug 17.

Abstract

Molecules that target microtubules have an important role in the treatment of cancer. A new class of inhibitors of tubulin polymerization based on the 2-(3,4,5-trimethoxybenzoyl)-2-dimethylamino-benzo[b]furan molecular skeleton was synthesized and evaluated for antiproliferative activity, inhibition of tubulin polymerization, and cell cycle effects. The most promising compound in this series was 2-(3,4,5-trimethoxybenzoyl)-3-dimethylamino-6-methoxy-benzo[b]furan, which inhibits cancer cell growth at nanomolar concentrations and interacts strongly with tubulin by binding to the colchicine site.

Publication types

  • Evaluation Study

MeSH terms

  • Animals
  • Antimitotic Agents / chemical synthesis
  • Antimitotic Agents / pharmacology*
  • Benzofurans / chemical synthesis
  • Benzofurans / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Humans
  • Inhibitory Concentration 50
  • Mice
  • Protein Binding
  • Structure-Activity Relationship
  • Tubulin Modulators / chemical synthesis
  • Tubulin Modulators / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Antimitotic Agents
  • Benzofurans
  • Tubulin Modulators