Salvinorin A is the main active psychotropic molecule in Salvia divinorum.
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Salvinorin A is the main active psychotropic molecule in Salvia divinorum.
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Salvinorin A can produce psychoactive experiences in humans with a typical duration of action being several minutes to an hour or so, depending on the method of ingestion.
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Salvinorin A is found with several other structurally related salvinorins.
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Salvinorin A is a trans-neoclerodane diterpenoid with the chemical formula C23H28O8.
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Unlike other known opioid-receptor ligands, salvinorin A is not an alkaloid, as it does not contain a basic nitrogen atom.
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Salvinorin A has no action at the 5-HT2A serotonin receptor, the principal molecular target responsible for the actions of 'classical' psychedelics such as LSD and mescaline.
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Salvinorin A has been shown to have effect on cannabinoid CB1 receptors.
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Salvinorin A is effectively deactivated by the gastrointestinal system, so alternative routes of administration must be used for better absorption.
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Salvinorin A is under preliminary research for its possible use as a scaffold in medicinal chemistry to develop new drugs for treating psychiatric diseases, such as addiction from cocaine dependence.
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SdCPS2 catalyzes the first committed reaction in the biosynthesis of salvinorin A by producing its characteristic clerodane scaffold.
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Salvinorin A is one of several structurally related salvinorins found in the Salvia divinorum plant.
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Salvinorin A is the only naturally occurring salvinorin that is known to be psychoactive.
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Salvinorin A is sometimes regulated together with its host, Salvia divinorum, due to its psychoactive and analgesic effects.
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Salvinorin A is not scheduled at the federal level in the United States.
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Salvinorin A is considered a Schedule 9 prohibited substance in Australia under the Poisons Standard.
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