A new diarylheptanoid from Alpinia officinarum promotes the differentiation of 3T3-L1 preadipocytes

Nat Prod Res. 2018 Mar;32(5):529-535. doi: 10.1080/14786419.2017.1327858. Epub 2017 May 25.

Abstract

A new diarylheptanoid, namely trans-(4R,5S)-epoxy-1,7-diphenyl-3-heptanone (1), and a new natural product, 7-(4″-hydroxy-3″-methoxyphenyl)-1-phenyl-hepta-4E,6E-dien-3-one (2), were obtained from the aqueous extract of Alpinia officinarum Hance, together with three other diarylheptanoids, 5-hydroxy-1,7-diphenyl-3-heptanone (3), 1,7-diphenyl-4E-en-3-heptanone (4) and 5-methoxy-1,7-diphenyl-3-heptanone (5). The structures were characterised mainly by analysing their physical data including IR, NMR and HRMS. This study highlights that the 4,5-epoxy moiety in 1 is rarely seen in diarylheptanoids. In addition, the five isolates were tested for their differentiation activity of 3T3-L1 preadipocytes. The results showed that these compounds could dose-dependently promote adipocyte differentiation without cytotoxicity (IC50 > 100 μM).

Keywords: 3T3-L1 preadipocytes; Alpinia officinarum Hance; diarylheptanoid; differentiation.

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology
  • Adipocytes / drug effects*
  • Alpinia / chemistry*
  • Animals
  • Cell Differentiation / drug effects
  • Diarylheptanoids / chemistry*
  • Diarylheptanoids / pharmacology*
  • Magnetic Resonance Spectroscopy
  • Mice
  • Molecular Structure
  • Plant Extracts / chemistry

Substances

  • Diarylheptanoids
  • Plant Extracts