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Leelakrishna Kondaveti

1 paper in the library · publishing 2005

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Synthesis and in vitro pharmacological studies of C(4) modified salvinorin A analogues.

Bioorganic & Medicinal Chemistry Letters October 1, 2005 David Y W Lee, Minsheng He, Leelakrishna Kondaveti et al.

Salvinorin A is the most potent naturally occurring opioid agonist with a high selectivity and affinity for kappa-opioid receptor. To explore its structure-activity relationships, modifications at the C(4) position have been studied and a series of salvinorin A derivatives were prepared. These C(4)-modified salvinorin A analogues were screened for binding and functional activities at the human...