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5-MeO-MT

This article is a stubmissing:
Subjective Effects
Interactions
Tolerance
History & Culture
Legality
5-MeO-MT molecule structure5-MeO-MT molecule structure
Chemical Class

5-MeO-MT is described as a tryptamine with psychedelic and entactogenic effects. It is described as structurally related to α-methyltryptamine and is reported to be highly potent, with occasional distribution on blotters. The substance was synthesized1, and its psychedelic effects in humans were first observed in 1976. It may act as a monoamine oxidase inhibitor, so caution is advised; rare reports describe it being sold as LSD.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold0.5-1 mg
Light1-2 mg
Moderate2-4 mg
Strong4-6 mg
Heavy6+ mg

Hospitalizations have been reported at oral doses as low as 8 mg, indicating a narrow margin of safety and the need for extreme caution with dosing.

Duration

Onset30-120 minutes

Subjective Effects

Subjective Effects not written up yet

Pharmacology

Pharmacodynamics

In the cited in vitro study, 5-MeO-AMT showed agonist activity at 5-HT2A and 5-HT2B receptors. It was described as the most potent 5-HT2A receptor ligand and agonist among the tryptamines evaluated in that study and the previous studies discussed by its authors, with an in vitro 5-HT2A EC50 of 2 nM and a 5-HT2B EC50 of 4 nM. 5-MeO-AMT was a very weak monoamine transporter inhibitor relative to its much higher potency at 5-HT2A and induced transporter-mediated release of dopamine and serotonin. It is also a weak MAO-A inhibitor.

Pharmacokinetics

Absorption & half-lifenot documented yetMetabolitesnone documented yet

Interactions

Interactions not written up yet

An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.

Check TripSit

Tolerance

Tolerance not written up yet

Harm Potential

Toxicity

Lethal Dosage

At least one death has been documented from overdose. Particularly sensitive individuals can experience overdose symptoms at doses as low as 20 mg, which falls within the normal range for most users. Hospitalizations have occurred at doses as low as 8 mg. The compound appears to have a narrow margin of safety, and oral consumption seems safer than insufflation.

Cardiovascular

Cardiac arrhythmia has been noted in overdose cases, likely due to the compound's sympathomimetic effects.

Seizure Risk

Moderate

Seizures have been noted in overdose cases. The seizure risk appears to be associated with the compound's sympathomimetic effects and may occur at doses that some users consider within normal range.

History & Culture

History & Culture not written up yet

Legality

Legality not written up yet

Article Status

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    Step 1 · Automated synthesis

    An autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.

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