Synthesis of salvinorin A analogues as opioid receptor probes

J Nat Prod. 2006 Jun;69(6):914-8. doi: 10.1021/np060094b.

Abstract

Several neoclerodanes, such as salvinorin A (1) and herkinorin (3), have recently been shown to possess opioid receptor activity in vitro and in vivo. To explore the structure-affinity relationships of this interesting class of compounds, we have synthesized a series of analogues from 1 isolated from Salvia divinorum. Here, we report the semisynthesis of neoclerodane diterpenes and their structure-affinity relationships at opioid receptors. This work will allow the further development of novel opioid receptor ligands.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Crystallography, X-Ray
  • Diterpenes* / chemical synthesis
  • Diterpenes* / chemistry
  • Diterpenes* / pharmacology
  • Diterpenes, Clerodane
  • Molecular Conformation
  • Molecular Structure
  • Plants, Medicinal / chemistry*
  • Receptors, Opioid / agonists*
  • Salvia / chemistry*
  • Structure-Activity Relationship

Substances

  • Diterpenes
  • Diterpenes, Clerodane
  • Receptors, Opioid
  • salvinorin A