Beilstein Journal of Organic Chemistry (Jan 2007)

8-epi-Salvinorin B: crystal structure and affinity at the κ opioid receptor

  • Thomas A. Munro,
  • Katharine K. Duncan,
  • Richard J. Staples,
  • Wei Xu,
  • Lee-Yuan Liu-Chen,
  • Cécile Béguin,
  • William A. Carlezon Jr.,
  • Bruce M. Cohen

DOI
https://doi.org/10.1186/1860-5397-3-1
Journal volume & issue
Vol. 3, no. 1
p. 1

Abstract

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There have been many reports of epimerization of salvinorins at C-8 under basic conditions, but little evidence has been presented to establish the structure of these compounds. We report here the first crystal structure of an 8-epi-salvinorin or derivative: the title compound, 2b. The lactone adopts a boat conformation with the furan equatorial. Several lines of evidence suggest that epimerization proceeds via enolization of the lactone rather than a previously proposed indirect mechanism. Consistent with the general trend in related compounds, the title compound showed lower affinity at the kappa opioid receptor than the natural epimer salvinorin B (2a). The related 8-epi-acid 4b showed no affinity.