Genkwalathins A and B, new lathyrane-type diterpenes from Daphne genkwa

Nat Prod Res. 2018 Aug;32(15):1782-1790. doi: 10.1080/14786419.2017.1402322. Epub 2017 Nov 20.

Abstract

Screening for new natural anti-neuroinflammatory compounds was performed with the traditional folk medicine Genkwa Flos, which potently inhibited nitric oxide (NO) production by LPS-activated microglial BV-2 cells. Two new lathyrane-type diterpenes, genkwalathins A (1) and B (2), and 14 known daphnane-type diterpenes (3-16) were isolated. The lathyrane-type diterpenes were isolated for the first time from the Thymelaeaceae family in this study. Compounds 1 and 2 moderately inhibited LPS-induced NO production in BV-2 cells without affecting cell viability, while six daphnane-type diterpenes (3, 4, 6, 7, 9 and 10) potently reduced NO production with IC50 values less than 1 μM, although they did display weak cytotoxicity. A structure-activity relationship study on the daphnane-type diterpenes indicated that the stereochemistry at C-19, the benzoate group at C-20, and the epoxide moiety could be important for their anti-neuroinflammatory effects.

Keywords: Daphne genkwa; Genkwa Flos; anti-neuroinflammatory; daphnane-type diterpene; lathyrane-type diterpene.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Cell Line
  • Cell Survival / drug effects
  • Daphne / chemistry*
  • Diterpenes / chemistry
  • Diterpenes / pharmacology*
  • Drug Evaluation, Preclinical
  • Lipopolysaccharides / pharmacology
  • Magnetic Resonance Spectroscopy
  • Mice
  • Microglia / cytology
  • Molecular Structure
  • Nitric Oxide / metabolism
  • Structure-Activity Relationship
  • Thymelaeaceae / chemistry

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Diterpenes
  • Lipopolysaccharides
  • lathyrane
  • Nitric Oxide
  • mezerein