Lipoxygenase inhibitory activity of Cuspidaria pulchra and isolated compounds

Nat Prod Res. 2015;29(11):1083-6. doi: 10.1080/14786419.2014.981182. Epub 2014 Nov 27.

Abstract

This work evaluated the in vitro inhibitory activity of the crude ethanolic extract from the aerial parts of Cuspidaria pulchra (Cham.) L.G. Lohmann against 15-lipoxygenase (15-LOX). The bioassay-guided fractionation of the n-butanol fraction, which displayed the highest activity, led to the isolation of three compounds: caffeoylcalleryanin (1), verbascoside (2) and 6-hydroxyluteolin-7-O-β-glucoside (3). Assessment of the ability of the isolated compounds to inhibit 15-LOX revealed that compounds 1, 2 and 3 exerted strong 15-LOX inhibitory activity; IC50 values were 1.59, 1.76 and 2.35 μM respectively. The XTT assay showed that none of the isolated compounds seemed to be significantly toxic.

Keywords: 15-lipoxygenase inhibitory activity; Arrabidaea; cytotoxic activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bignoniaceae / chemistry*
  • Caffeic Acids / chemistry
  • Caffeic Acids / isolation & purification
  • Caffeic Acids / pharmacology*
  • Glucosides / chemistry
  • Glucosides / isolation & purification
  • Lipoxygenase Inhibitors / pharmacology*
  • Luteolin / chemistry
  • Luteolin / isolation & purification
  • Molecular Structure
  • Phenols / chemistry
  • Phenols / isolation & purification
  • Plant Components, Aerial / chemistry
  • Plant Extracts / pharmacology*

Substances

  • 6-hydroxyluteolin-7-O-glucoside
  • Caffeic Acids
  • Glucosides
  • Lipoxygenase Inhibitors
  • Phenols
  • Plant Extracts
  • caffeoylcalleryanin
  • acteoside
  • Luteolin