Salvinorin A

Salvinorin A

 

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We present to you Salvinorin A :

Salvinorin A is the main active psychotropic molecule in Salvia divinorum, a Mexican plant which has a long history of use as an entheogen by indigenous Mazatec shamans. Salvinorin A is a hallucinogenic compound with dissociative effects.

It is structurally quite distinct from other naturally occurring hallucinogens such as N,N-dimethyltryptamine, psilocybin, and mescaline and from synthetic hallucinogens such as lysergic acid diethylamide (LSD), and ketamine.

Salvinorin A has been reported to be the most potent naturally occurring psychoactive drug known to date, with an effective dose in humans in the 200- to 1,000-µg range when smoked. In that way Salvinorin A’s qualitative potency may be compared with LSD, though it is otherwise dissimilar, having quite different effects and timeframes.

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.

Salvinorin A is found together with several other structurally related salvinorins. Salvinorin is a trans-neoclerodane diterpenoid. It acts as a kappa opioid receptor agonist and is the first known compound acting on this receptor that is not an alkaloid. Salvinorin A was isolated in 1982 by Alfredo Ortega in Mexico. Its pharmacological mechanism was elucidated in the laboratory of Bryan L. Roth.

Salvinorin A is a trans-neoclerodane diterpenoid, chemical formula C23H28O8.[2] Unlike other known opioid-receptor ligands, salvinorin A is not an alkaloid — it does not contain a basic nitrogen atom. Salvinorin A has no actions at the 5-HT2A serotonin receptor, the principal molecular target responsible for the actions of ‘classical’ psychedelics such as LSD and mescaline.

Salvinorin A is the most potent naturally-occurring psychoactive compound known. It is active at doses as low as 200 µg. Recent research has shown that salvinorin A is a potent and selective κ (kappa) opioid receptor agonist. It has been reported that the effects of salvinorin A in mice are blocked by kappa opioid receptor antagonists.[

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