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Jian-Guo Li

3 papers in the library · publishing 2005-2006

Papers

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

Bioorganic & Medicinal Chemistry Letters November 1, 2006 David Y W Lee, Minsheng He, Lee-Yuan Liu-Chen et al.

Salvinorin A, a compound isolated from the plant Salvia divinorum, is a potent and highly selective agonist for the kappa opioid receptor. For exploration of its structure and activity relationships, further modifications, such as reduction 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...

Synthesis and in vitro evaluation of salvinorin A analogues: effect of configuration at C(2) and substitution at C(18).

Bioorganic & Medicinal Chemistry Letters September 1, 2006 Cécile Béguin, Michele R Richards, Jian-Guo Li et al.

kappa-opioid receptor ligands have raised interest for their apparent effects on mood. The potent and selective kappa-agonist salvinorin A has short-lasting (15min) depressive-like effects in rats in behavioral models used to study mood disorders. Two series of salvinorin derivatives modified at C(2) and C(18), respectively, were synthesized and their kappa-opioid receptor affinities,...

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...