Anticancer activities of novel chalcone and bis-chalcone derivatives

Bioorg Med Chem. 2006 May 15;14(10):3491-5. doi: 10.1016/j.bmc.2006.01.003. Epub 2006 Jan 24.

Abstract

A series of novel chalcones and bis-chalcones containing boronic acid moieties has been synthesized and evaluated for antitumor activity against the human breast cancer MDA-MB-231 (estrogen receptor-negative) and MCF7 (estrogen receptor-positive) cell lines and against two normal breast epithelial cell lines, MCF-10A and MCF-12A. These molecules inhibited the growth of the human breast cancer cell lines at low micromolar to nanomolar concentrations, with five of them (1-4, 9) showing preferential inhibition of the human breast cancer cell lines. Furthermore, bis-chalcone 8 exhibited a more potent inhibition of colon cancer cells expressing wild-type p53 than of an isogenic cell line that was p53-null.

Publication types

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

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology*
  • Boronic Acids / chemistry*
  • Boronic Acids / pharmacology*
  • Breast Neoplasms / drug therapy*
  • Cell Line, Tumor
  • Chalones / chemistry*
  • Chalones / pharmacology*
  • Colonic Neoplasms / drug therapy*
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • Female
  • Humans
  • Lethal Dose 50
  • Molecular Structure
  • Piperidines / chemistry*
  • Piperidines / pharmacology*

Substances

  • 3,5-bis(4-boronic acid-benzylidene)-1-methylpiperidin-4-one
  • Antineoplastic Agents
  • Boronic Acids
  • Chalones
  • Piperidines