Oxygenated sesquiterpenoids from a nonpoisonous sardinian chemotype of giant fennel (Ferula communis)

J Nat Prod. 2001 Mar;64(3):393-5. doi: 10.1021/np000468f.

Abstract

The roots of the nonpoisonous chemotype of giant fennel (Ferula communis) from Sardinia afforded a novel cadinanetriol (1), whose structure was established by spectroscopic data and confirmed by synthesis from the E,E-Delta (1(10),5) germacradiene allohedycariol. A number of known compounds were also identified. Despite the lack of morphological differences, a broad chemical diversity exists within giant fennel, underlying the contrasting data on its poisonous properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ferula / chemistry*
  • Italy
  • Plants, Medicinal*
  • Plants, Toxic*
  • Polycyclic Sesquiterpenes
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / isolation & purification*
  • Species Specificity

Substances

  • Polycyclic Sesquiterpenes
  • Sesquiterpenes
  • cadinanetriol