Structure-activity relationships of tanshinones in activating Nrf2. A DFT study and implications for multifunctional antioxidant discovery

Nat Prod Commun. 2014 Apr;9(4):453-4.

Abstract

A series of recent studies reveal that tanshinones, derived from the traditional Chinese herbal medicine Salvia miltiorrhiza Bunge, are promising multifunctional antioxidants by activating nuclear factor (erythroid-derived 2) - like 2 (Nrf2). It is thus of great interest to elucidate their structure-activity relationships (SAR) for Nrf2 activation. In this study, two theoretical parameters characterizing the electron-abstracting potential, namely, electron affinity (EA) and energy level of the lowest unoccupied molecular orbital (ELUMO), are calculated by a density functional theory (DFT) method. By these parameters, we provide a satisfactory explanation to the SAR oftanshinones for activating Nrf2, which is helpful to find new multifunctional antioxidants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Models, Biological
  • Models, Chemical
  • Molecular Structure
  • Quinones / chemistry*
  • Quinones / pharmacology*
  • Structure-Activity Relationship

Substances

  • Quinones