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A review of salvinorin analogs and their kappa-opioid receptor activity
Jeremy J Roach1, Ryan A Shenvi1
1Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.
Abstract:
The plant metabolite salvinorin A potently and selectively agonizes the human kappa-opioid receptor, an emerging target for next-generation analgesics. Here we review analogs of the salvinorin chemotype and their effects on selectivity, affinity and potency. Extensive peripheral modifications using isolated salvinorin A have delivered a trove of SAR information. More deep-seated changes are now possible by advances in chemical synthesis.
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