Synthesis and anti-tumor activity of novel combretastatins: combretocyclopentenones and related analogues

Bioorg Med Chem Lett. 2002 Aug 5;12(15):1955-8. doi: 10.1016/s0960-894x(02)00321-9.

Abstract

A series of 2-(3,4,5-trimethoxyphenyl)-3-arylcyclopent-2-ene-1-ones (8a-8e) and their related analogues, including pentenone 9a, pentenol 10a, pentene 12a, and furane 15, were synthesized and evaluated for cytotoxicity against murine and human tumor cell lines. Compounds 8a-c, 8e and 9a showed strong cytotoxicity with IC(50) values in the range of 8-34ng/mL. Compound 8e exhibited significant anti-tumor activity in BDF1 mice bearing Lewis lung carcinoma cells with an inhibition ratio of 59%.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Bibenzyls / chemical synthesis*
  • Bibenzyls / pharmacology*
  • Carcinoma, Lewis Lung / drug therapy
  • Cyclopentanes / chemistry*
  • Cyclopentanes / pharmacology*
  • Drug Screening Assays, Antitumor
  • Humans
  • Inhibitory Concentration 50
  • Mice
  • Stereoisomerism
  • Stilbenes*
  • Structure-Activity Relationship
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Bibenzyls
  • Cyclopentanes
  • Stilbenes
  • combretastatin
  • cyclopentenone