Synthesis of O-prenylated and O-geranylated derivatives of 5-benzylidene2,4-thiazolidinediones and evaluation of their free radical scavenging activity as well as effect on some phase II antioxidant/detoxifying enzymes

Bioorg Med Chem Lett. 2007 Mar 1;17(5):1149-54. doi: 10.1016/j.bmcl.2006.12.040. Epub 2006 Dec 15.

Abstract

A series of 5-arylidene-2,4-thiazolidinediones and its geranyloxy or prenyloxy derivative were synthesized and studied for their radical scavenging activity using 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. Their comparable scavenging activities were expressed as IC50 value. Compounds 2c, 2d, 4d, and 6a showed appreciable radical scavenging activities. The vanillin based thiazolidinedione compound 2c displayed highest activity comparable to that of alpha-tocopherol. But in vivo, compound 6a showed better results in inducing phase II detoxifying/antioxidative enzyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants
  • Benzaldehydes
  • Biphenyl Compounds
  • Free Radical Scavengers / chemical synthesis*
  • Free Radical Scavengers / chemistry
  • Inhibitory Concentration 50
  • Picrates
  • Protein Prenylation
  • Structure-Activity Relationship
  • Thiazolidinediones / chemical synthesis*
  • Thiazolidinediones / chemistry
  • alpha-Tocopherol

Substances

  • Antioxidants
  • Benzaldehydes
  • Biphenyl Compounds
  • Free Radical Scavengers
  • Picrates
  • Thiazolidinediones
  • vanillin
  • 1,1-diphenyl-2-picrylhydrazyl
  • alpha-Tocopherol