β-Secretase inhibition by C-methylisoflavones from Abronia nana

Nat Prod Res. 2019 Jun;33(12):1705-1712. doi: 10.1080/14786419.2018.1431637. Epub 2018 Jan 31.

Abstract

The methanol extract of Abronia nana suspension cultures were subjected to column chromatography to identify potential inhibitors of β-secretase, which is a major factor in Alzheimer's disease development. Two new C-methylisoflavones boeravinone T (1) and U (4) were isolated with three knowns boeravinone B (2), J (3) and X (5). The half-maximal inhibitory concentration (IC50) values of compounds 1-5 were 18.29, 8.57, 7.87, 12.02 and 5.30 μM, respectively. The most potent 5, non-competitively inhibited β-secretase [inhibition constant (Ki) = 3.79 μM]. Compounds 1-5 did not inhibit other proteases such as chymotrypsin, trypsin and elastase at concentrations up to 1 mM, indicating that they were relatively specific inhibitors of β-secretase. A free hydroxyl group at C-3 position of the C-methylisoflavone skeleton appeared to be responsible for the stronger inhibitory activity against β-secretase.

Keywords: -methylisoflavones; boeravinone X; β-secretase.

MeSH terms

  • Alzheimer Disease / etiology
  • Amyloid Precursor Protein Secretases / antagonists & inhibitors*
  • Benzopyrans / isolation & purification
  • Benzopyrans / pharmacology
  • Flavonoids / isolation & purification
  • Flavonoids / pharmacology
  • Humans
  • Inhibitory Concentration 50
  • Nyctaginaceae / chemistry*
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Structure-Activity Relationship
  • Substrate Specificity

Substances

  • Benzopyrans
  • Flavonoids
  • Plant Extracts
  • boeravinone B
  • boeravinone X
  • Amyloid Precursor Protein Secretases