Phytotoxicity of secondary metabolites isolated from Flourensia oolepis S.F.Blake

Chem Biodivers. 2013 Jul;10(7):1295-304. doi: 10.1002/cbdv.201200204.

Abstract

The aim of this study was to isolate the active principles of Flourensia oolepis S.F.Blake (Asteraceae), which completely inhibited the germination of Raphanus sativus seeds at 10 mg/ml. Flavanone pinocembrin and sesquiterpene ilicol, were isolated by bioassay-guided fractionation. They were active both against monocot and dicot seeds. Pinocembrin was the most active compound, with an IC50 (germination) value of 0.24, 3.40, 3.28, and 3.55 mM against Panicum miliaceum, Avena sativa, Lactuca sativa, and R. sativus, respectively; ilicol, however, exhibited IC50 (germination) values of 0.67, 2.73, 5.25, and 9.66 mM for the same species, respectively. Pinocembrin and ilicol inhibited root growth and showed IC50 (root growth) values of 0.199, 14.68, 8.05, 7.69 mM, and 1.22, 2.90, 7.35, 8.07 mM, against P. miliaceum, A. sativa, L. sativa, and R. sativus, respectively. Pinocembrin and ilicol reduced Allium cepa cell division without chromosome aberrations.

Keywords: Flourensia oolepis; Ilicol; Phytotoxic activity; Pinocembrin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allium / growth & development
  • Asteraceae / chemistry*
  • Asteraceae / metabolism*
  • Flavanones / chemistry*
  • Flavanones / isolation & purification
  • Flavanones / pharmacology
  • Flavanones / toxicity
  • Germination / drug effects
  • Mitosis / drug effects
  • Plant Components, Aerial / chemistry
  • Plant Components, Aerial / metabolism
  • Plant Extracts / toxicity*
  • Plant Roots / drug effects
  • Plant Roots / growth & development
  • Raphanus / growth & development
  • Seeds / growth & development
  • Sesquiterpenes / chemistry*
  • Sesquiterpenes / isolation & purification
  • Sesquiterpenes / pharmacology
  • Sesquiterpenes / toxicity*

Substances

  • Flavanones
  • Plant Extracts
  • Sesquiterpenes
  • ilicol
  • pinocembrin