Diarylheptanoids with free radical scavenging and hepatoprotective activity in vitro from Curcuma longa

Planta Med. 2001 Dec;67(9):876-7. doi: 10.1055/s-2001-18860.

Abstract

Assay-guided fractionation of the EtOAc soluble fraction of the rhizomes of Curcuma longa furnished three DPPH free radical scavenging diarylheptanoids, curcumin (1), demethoxycurcumin (2), and bisdemethoxycurcumin (3). Compounds 1-3 showed the DPPH radical scavenging effects with IC(50) values of 2.8, 39.2, 308.7 microM, respectively. L-Ascorbic acid and resveratrol as positive controls exhibited IC(50) values of 22.5 and 25.0 microM, respectively. Compounds 1-3 showed significant hepatoprotective effects on tacrine-induced cytotoxicity in human liver-derived Hep G2 cells. The EC(50) values of 1-3 are 86.9, 70.7, and 50.2 microM, respectively. Silybin (EC(50) = 69.0 microM) and silychristin (EC(50) = 82.7 microM) were used as positive controls.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Coumaric Acids / chemistry
  • Coumaric Acids / isolation & purification
  • Coumaric Acids / pharmacology*
  • Curcuma*
  • Curcumin / analogs & derivatives*
  • Curcumin / chemistry
  • Curcumin / isolation & purification
  • Curcumin / pharmacology*
  • Diarylheptanoids
  • Free Radical Scavengers / chemistry
  • Free Radical Scavengers / isolation & purification
  • Free Radical Scavengers / pharmacology*
  • Humans
  • Inhibitory Concentration 50
  • Rhizome / chemistry
  • Tumor Cells, Cultured / drug effects

Substances

  • Coumaric Acids
  • Diarylheptanoids
  • Free Radical Scavengers
  • bisdemethoxycurcumin
  • Curcumin
  • demethoxycurcumin