salvinorin การใช้

• Salvinorin A is found with several other structurally related salvinorins.
• Salvinorin A is found with several other structurally related salvinorins.
• Additional oxidation and cyclization clerodane pyrophosphate concludes the biosynthesis of salvinorin A.
• Salvinorin A can be synthesized from the inactive salvinorin B by acetylation.
• Salvinorin A can be synthesized from the inactive salvinorin B by acetylation.
• The de-acetylated analog salvinorin B is devoid of human activity.
• Salvinorin's potency should not be confused with toxicity.
• Thus, like most hallucinogens, salvinorin A has low abuse potential.
• Salvinorin A is a " trans "-neoclerodane basic nitrogen atom.
• In addition to Salvinorin _ A, other psychoactives may also be applied sublingually.
• Salvinorin A is the first documented diterpene hallucinogen.
• Nor does it contain nitrogen, which makes Salvinorin A unusual as a psychoactive molecule.
• Salvinorin A is considered a dissociative.
• Salvinorin A was first described and named in 1982 by Alfredo Ortega and colleagues in Mexico.
• In experimental models of colitis in mice, Salvinorin A has shown to have CB1 receptors.
• THC and salvinorin A are exceptions.
• Salvinorin A "'seems "'to be the only active naturally occurring salvinorin.
• Salvinorin A "'seems "'to be the only active naturally occurring salvinorin.
• Interestingly, salvinorin A shows atypical properties as an agonist of the KOR relative to other KOR agonists.
• Salvinorin A is one of several structurally related salvinorins found in the " Salvia divinorum " plant.