A novel franchetine type norditerpenoid isolated from the roots of Aconitum carmichaeli Debx. with potential analgesic activity and less toxicity

Bioorg Med Chem Lett. 2012 Jul 1;22(13):4444-6. doi: 10.1016/j.bmcl.2012.04.132. Epub 2012 May 14.

Abstract

Further investigation on the phytochemistry of the plant Aconitum carmichaeli Debx. led to isolate a new franchetine type C(19)-diterpenoid alkaloid, guiwuline 1. Its structure was established on the basis of the spectroscopic data (1D and 2D NMR, HRESIMS, UV, IR). In mouse hot-plate test and acute toxicity assay, compound 1 exhibited potential analgesic activity (ED(50), 15 mg/kg) and showed little toxicity to mice (LD(50), 500 mg/kg). The results indicate that compound 1 may be used as a lead molecule to develop novel analgesic agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aconitum / chemistry*
  • Alkaloids / chemistry*
  • Alkaloids / pharmacology
  • Alkaloids / toxicity
  • Analgesics / chemistry*
  • Analgesics / pharmacology
  • Analgesics / toxicity
  • Animals
  • Behavior, Animal / drug effects
  • Diterpenes / chemistry*
  • Diterpenes / pharmacology
  • Diterpenes / toxicity
  • Magnetic Resonance Spectroscopy
  • Mice
  • Molecular Conformation
  • Plant Roots / chemistry
  • Spectrometry, Mass, Electrospray Ionization
  • Spectrophotometry, Infrared
  • Spectrophotometry, Ultraviolet
  • Temperature
  • Toxicity Tests

Substances

  • Alkaloids
  • Analgesics
  • Diterpenes