5-Ethoxy-αMT
Chemical compound
5-Ethoxy-αMT (5-EtO-αMT) is a psychedelic and stimulant drug of the tryptamine class. It is closely related to αMT (alpha-methyltryptamine) and 5-MeO-αMT (5-methoxy-alpha-methyltryptamine), differing by the presence of an ethoxy group at the 5-position of the indole ring.
Chemical structure and properties
5-Ethoxy-αMT is a synthetic compound that belongs to the tryptamine family. Its chemical structure consists of an indole ring, which is a bicyclic structure composed of a benzene ring fused to a pyrrole ring, with an ethoxy group attached at the 5-position. The presence of the alpha-methyl group distinguishes it from other tryptamines, contributing to its unique pharmacological properties.
Pharmacology
5-Ethoxy-αMT acts primarily as a serotonin receptor agonist, particularly at the 5-HT2A receptor, which is believed to be responsible for its psychedelic effects. It may also have activity at other serotonin receptors, as well as potential interactions with dopamine and norepinephrine systems, contributing to its stimulant properties.
Effects
The effects of 5-Ethoxy-αMT are reported to be similar to those of other psychedelic tryptamines, such as psilocybin and DMT, but with a longer duration of action. Users have described experiences of altered perception, enhanced mood, and increased sensory awareness. The stimulant effects may include increased energy and alertness.
Safety and toxicity
As with many research chemicals, the safety profile of 5-Ethoxy-αMT is not well-established. There is limited data on its toxicity, potential for addiction, and long-term effects. Users should exercise caution and be aware of the potential risks associated with its use.
Legal status
The legal status of 5-Ethoxy-αMT varies by country. In some jurisdictions, it may be classified as a controlled substance, while in others it may be legal or unregulated. It is important for individuals to be aware of the laws in their area before possessing or using this compound.
Related compounds
Related pages
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Contributors: Prab R. Tumpati, MD