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Douglas J Sheffler

2 papers in the library · 242 citations · publishing 2003-2005

Papers

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Identification of the molecular mechanisms by which the diterpenoid salvinorin A binds to kappa-opioid receptors.

Biochemistry June 21, 2005 Feng Yan, Philip D Mosier, Richard B Westkaemper et al. 91 citations

Salvinorin A is a naturally occurring hallucinogenic diterpenoid from the plant Salvia divinorumthat selectively and potently activates kappa-opioid receptors (KORs). Salvinorin A is unique in that it is the only known lipid-like molecule that selectively and potently activates a G-protein coupled receptor (GPCR), which has as its endogenous agonist a peptide; salvinorin A is also the only...

DOI: 10.1021/bi050490d (opens in new tab) Full text (opens in new tab) Opioid receptors Opioid receptor binding Receptor activation Receptor selectivity +18

Salvinorin A: the "magic mint" hallucinogen finds a molecular target in the kappa opioid receptor.

TIPS - Trends in Pharmacological Sciences March 1, 2003 Douglas J Sheffler, Bryan L. Roth 151 citations

Salvinorin A, a neoclerodane diterpene, is the most potent naturally occurring hallucinogen known and rivals the synthetic hallucinogen lysergic acid diethylamide in potency. Recently, the molecular target of salvinorin A was identified as the kappa opioid receptor (KOR). Salvinorin A represents the only known non-nitrogenous KOR selective agonist. Based on the selectivity of salvinorin A for...