Synthesis, biological evaluation of 1,1-diarylethylenes as a novel class of antimitotic agents

ChemMedChem. 2009 Nov;4(11):1912-24. doi: 10.1002/cmdc.200900290.

Abstract

The cytotoxic activities of 23 new isocombretastatin A derivatives with modifications on the B-ring were investigated. Several compounds exhibited excellent antiproliferative activity at nanomolar concentrations against a panel of human cancer cell lines. Compounds isoFCA-4 (2 e), isoCA-4 (2 k) and isoNH(2)CA-4 (2 s) were the most cytotoxic, and strongly inhibited tubulin polymerization with IC(50) values of 4, 2 and 1.5 microM, respectively. These derivatives were found to be 10-fold more active than phenstatin and colchicine with respect to growth inhibition but displayed similar activities as tubulin polymerization inhibitors. In addition, cell cycle arrest in the G(2)/M phase and subsequent apoptosis was observed in three cancer cell lines when treated with these compounds. The disruptive effect of 2 e, 2 k and 2 s on the vessel-like structures formed by human umbilical vein endothelial cells (HUVEC) suggest that these compounds may act as vascular disrupting agents. Both compounds 2 k and 2 s have the potential for further prodrug modification and development as vascular disrupting agents for treatment of solid tumors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimitotic Agents / chemical synthesis*
  • Antimitotic Agents / chemistry
  • Antimitotic Agents / toxicity
  • Benzophenones / pharmacology
  • Cell Division
  • Cell Line, Tumor
  • Colchicine / pharmacology
  • G2 Phase
  • Humans
  • Organophosphates / pharmacology
  • Stilbenes / chemical synthesis
  • Stilbenes / chemistry*
  • Stilbenes / toxicity
  • Tubulin Modulators / chemical synthesis*
  • Tubulin Modulators / chemistry
  • Tubulin Modulators / toxicity

Substances

  • Antimitotic Agents
  • Benzophenones
  • Organophosphates
  • Stilbenes
  • Tubulin Modulators
  • phenstatin phosphate
  • fosbretabulin
  • Colchicine