Publication | Open Access
8-<i>epi</i>-Salvinorin B: crystal structure and affinity at the κ opioid receptor
92
Citations
22
References
2007
Year
Crystal StructurePharmaceutical ScienceDrug TargetBioorganic ChemistryPharmacotherapyIndirect MechanismTitle CompoundChemical BiologyPharmaceutical ChemistryMolecular PharmacologyMedicinal ChemistryFuran EquatorialStereoselective SynthesisBiochemistryReceptor (Biochemistry)Mechanism Of ActionNeuropharmacologyκ Opioid ReceptorPharmacologyEnantioselective SynthesisNatural SciencesMedicineDrug Discovery
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.
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