Structural antitumoral activity relationships of synthetic chalcones

Int J Mol Sci. 2009 Jan;10(1):221-231. doi: 10.3390/ijms10010221. Epub 2009 Jan 9.

Abstract

Relationships between the structural characteristic of synthetic chalcones and their antitumoral activity were studied. Treatment of HepG2 cells for 24 h with synthetic 2'-hydroxychalcones resulted in apoptosis induction and dose-dependent inhibition of cell proliferation. The calculated reactivity indexes and the adiabatic electron affinities using the DFT method including solvent effects, suggest a structure-activity relationship between the Chalcones structure and the apoptosis in HepG2 cells. The absence of methoxy substituents in the B ring of synthetic 2'-hydroxychalcones, showed the mayor structure-activity pattern along the series.

Keywords: Antitumoral activity; DFT; structure-activity relationships.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Cell Proliferation / drug effects
  • Chalcones / chemistry
  • Chalcones / pharmacology*
  • Hep G2 Cells
  • Humans
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Chalcones