New Cyclic Diarylheptanoids from Platycarya strobilacea

Molecules. 2020 Dec 20;25(24):6034. doi: 10.3390/molecules25246034.

Abstract

Five new cyclic diarylheptanoids (platycary A-E, compounds 1-5) and three previously identified analogues (i.e., phttyearynol (compound 6), myricatomentogenin (compound 7), and juglanin D (compound 8)) were isolated from the stem bark of Platycarya strobilacea. The structures of these compounds were determined using NMR, HRESIMS, and electronic circular dichroism (ECD) data. The cytotoxicity of compounds 1-5 and their ability to inhibit nitric oxide (NO) production, as well as protect against the corticosterone-induced apoptosis of Pheochromocytoma (PC12) cells, were evaluated in vitro using the appropriate bioassays. Compounds 1 and 2 significantly inhibited the corticosterone-induced apoptosis of PC12 cells at a concentration of 20 μΜ.

Keywords: Juglandaceae; Platycarya strobilacea; corticosterone-induced apoptosis; cyclic diarylheptanoid.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Survival
  • Diarylheptanoids / isolation & purification
  • Diarylheptanoids / pharmacology*
  • Humans
  • Juglandaceae / chemistry*
  • Molecular Structure*
  • Neoplasms / drug therapy*
  • Neoplasms / pathology
  • Nitric Oxide / metabolism
  • Plant Extracts / pharmacology*
  • Rats

Substances

  • Diarylheptanoids
  • Plant Extracts
  • Nitric Oxide