Synthesis and antitumor activity of some analogues of flavone acetic acid

Anticancer Drug Des. 1996 Apr;11(3):243-52.

Abstract

Some coumarin-, flavonol- and flavanon-acetic acids are described. The cytotoxicity of the synthesized compounds was determined on a human colon carcinoma cell line (LoVo) through evaluation of neutral red uptake, performed by the Riddel method. All tested derivatives were able to induce a statistically significant reduction of lysosomal neutral red uptake at 5 x 10(-5) M concentration. Some compounds were more active than the reference compound flavon-8-acetic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / chemical synthesis*
  • Acetates / therapeutic use
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / therapeutic use
  • Colonic Neoplasms / drug therapy*
  • Coumarins / chemical synthesis
  • Coumarins / therapeutic use
  • Flavonoids / chemical synthesis*
  • Flavonoids / therapeutic use
  • Humans
  • Structure-Activity Relationship
  • Tumor Cells, Cultured

Substances

  • Acetates
  • Antineoplastic Agents
  • Coumarins
  • Flavonoids