α-Methyltryptamine is a psychedelic, stimulant, and entactogendrug of the tryptamine class. It was originally developed as an antidepressant by workers at Upjohn in the 1960s, and was used briefly as an antidepressant in Russia under the trade name Indopan before being discontinued.
The synthesis of αMT can be accomplished through several different routes, the two most widely known being the Nitroaldol Condensation between indole-3-carboxaldehyde and nitroethane under ammonium acetate catalysis and the condensation between indole-3-acetone and hydroxylamine followed by reduction of the obtained ketoxime with lithium aluminum hydride.
αMT has been shown as a reversibleinhibitor of the enzymemonoamine oxidasein-vitro and in-vivo. In rats the potency of αMT as an MAO-A inhibitor in the brain was approximately equal to that of harmaline at equimolar doses. Dexamphetamine did not enhance the 5-hydroxytryptophan-induced rise of serotonin at any level. A typical dose of harmaline for MAO inhibition is 150 mg, higher than any typical αMT dose so αMT's MAOI activity at typical doses will be significant but not total. The danger rises exponentially as αMT doses approach 150 mg due to increased monoamine release and increased MAO inhibition.
Metabolism
2-Oxo-αMT, 6-hydroxy-αMT, 7-hydroxy-αMT and 1′-hydroxy-αMT were detected as metabolites of αMT in male Wistar rats
Dosage and effects
Under the trade name Indopan, 5-10 milligrams were used for an antidepressant effect. With 20–30 milligrams, euphoria, empathy, and psychedelic effects become apparent and can last as long as 12 hours. A dose exceeding 40 mg is generally considered strong. In rare cases or extreme doses, the duration of effects might exceed 24 hours. Users report that αMT in freebaseform is smoked, with doses between and 2 and 5 milligrams. Reported side effects include anxiety, restlessness, muscle tension, jaw tightness, pupil dilation, tachycardia, headaches, nausea, and vomiting, among other effects that might commonly be attributed to LSD, psilocybin, DMT, and MDMA, such as open-eye visuals, closed eye visuals and an altered state of mind. In spite of some reported experiential similarities to MDMA, the chemicals are structurally unrelated; αMT is a tryptamine while MDMA is a phenethylamine. Like many other serotonin releasing agents, αMT's analogα-ethyltryptamine has been shown to produce long-lasting serotonergic neurotoxicity at very high doses. It is possible that αMT causes the same neurotoxicity.
Legality
Australia
The 5-Methoxy analogue, 5-MeO-αMT is schedule 9 in Australia and αMT would be controlled as an analogue of this.
αMT is listed under the Narcotics Act in schedule 1 in Germany.
Austria
αMT is placed under Austrian law Group 6.
Hungary
αMT was controlled on the Schedule C list in Hungary in 2013.
Slovakia
αMT was placed in 2013 on the List of Hazardous Substances in Annex, § 2 in Slovakia.
Slovenia
αMT appeared on the Decree on Classification of Illicit Drugs in Slovenia.
Lithuania
In Lithuania, αMT is controlled as a tryptamine derivative put under control in the 1st list of Narcotic Drugs and Psychotropic Substances which use is prohibited for medical purposes.
Spain
αMT is legal in Spain.
Sweden
health ministry :sv:Statens folkhälsoinstitut|Statens folkhälsoinstitut classified αMT as "health hazard" under the act :sv:Lagen om förbud mot vissa hälsofarliga varor|Lagen om förbud mot vissa hälsofarliga varor as of Mar 1, 2005, in their regulation SFS 2005:26 listed as alfa-metyltryptamin , making it illegal to sell or possess.
AMT, alfa-methyltryptamine is a controlled drug in Finland
Reported deaths
Deaths from αMT are rare but as a powerful monoamine releaser, injury can occur when excessive doses are taken or when taken with drugs such as MAOIs. Most fatalities are not verified but those which are involve excessive doses or coingestion with other drugs. A British teenager died after consuming 1 g of αMT in August 2013.