Title of article :
Synthetic studies on neoclerodane diterpenes from Salvia splendens: oxidative modifications of ring A
Author/Authors :
Gianfranco Fontana، نويسنده , , Giuseppe Savona، نويسنده , , Benjam?n Rodr?guez، نويسنده , , Christina M. Dersch، نويسنده , , Richard B. Rothman، نويسنده , , Thomas E. Prisinzano، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Abstract :
Salvinorin A (1), a neoclerodane diterpene from the hallucinogenic mint Salvia divinorum, is the only known naturally occurring non-nitrogenous and specific κ-opioid agonist. Some oxidative modifications of the A ring in the congeners of 1 isolated from Salvia splendens salviarin, splenolide B, splendidin, and in the non-natural 8-epi-salviarin gave new derivatives, some of which were tested as agonists at opioid receptors. However, none of these compounds was active. The presence of the C-18, C-19 lactone could be at the origin of the observed lack of binding affinity.
Keywords :
Neoclerodane diterpenes , Opioid receptors , Semisynthetic derivatives , Salvia splendens
Journal title :
Tetrahedron
Journal title :
Tetrahedron