5-Methoxy-7,N,N-trimethyltryptamine: Difference between revisions

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{{Short description|Chemical compound}}
== 5-Methoxy-7,N,N-trimethyltryptamine ==
{{Chembox
| ImageFile = 5-MeO-7-TMT.png
| ImageSize = 250px
| ImageAlt =
| IUPACName = 5-Methoxy-7,N,N-trimethyltryptamine
| OtherNames = 5-MeO-7-TMT
}}


'''5-Methoxy-7,N,N-trimethyltryptamine''' ('''5-MeO-7-TMT''') is a [[psychedelic]] compound belonging to the [[tryptamine]] class. It is structurally related to other tryptamines such as [[5-MeO-DMT]] and [[7-MeO-MiPT]].
[[File:5-MeO-7-TMT.png|thumb|right|Chemical structure of 5-Methoxy-7,N,N-trimethyltryptamine]]


==Chemical structure==
'''5-Methoxy-7,N,N-trimethyltryptamine''' (5-MeO-7-TMT) is a synthetic compound belonging to the class of [[tryptamines]], which are structurally related to the naturally occurring neurotransmitter [[serotonin]]. This compound is of interest in the field of [[psychopharmacology]] due to its potential psychoactive effects.
5-MeO-7-TMT is a derivative of [[tryptamine]], which is a core structure in many [[psychoactive]] compounds. The chemical structure of 5-MeO-7-TMT includes a methoxy group at the 5-position and a trimethylated nitrogen at the 7-position of the indole ring.


==Pharmacology==
=== Chemical Structure ===
The pharmacological properties of 5-MeO-7-TMT are not well-documented, but it is believed to act as a [[serotonin receptor]] agonist, similar to other tryptamines. This action is thought to be responsible for its psychedelic effects.
5-MeO-7-TMT is a derivative of the tryptamine molecule, characterized by the presence of a methoxy group at the 5-position and three methyl groups attached to the nitrogen atom at the 7-position. The chemical formula for 5-MeO-7-TMT is C14H20N2O.


==Effects==
=== Pharmacology ===
The effects of 5-MeO-7-TMT are not extensively studied, but it is presumed to produce [[hallucinogenic]] and [[psychedelic]] effects similar to other compounds in the tryptamine family. Users may experience altered [[perception]], [[mood]], and [[cognition]].
The pharmacological properties of 5-MeO-7-TMT are not well-documented, but it is believed to interact with the [[serotonin receptor|serotonin receptors]] in the brain, similar to other tryptamines. This interaction may result in altered perception, mood, and cognition, although specific effects and potency are not well-studied.


==Legal status==
=== Synthesis ===
The legal status of 5-MeO-7-TMT varies by country. In some jurisdictions, it may be classified as a controlled substance, while in others it may not be specifically regulated.
The synthesis of 5-MeO-7-TMT involves the modification of the tryptamine backbone. The process typically includes the introduction of a methoxy group at the 5-position and the methylation of the nitrogen atom. These chemical modifications are carried out using standard organic synthesis techniques.


==Synthesis==
=== Potential Effects ===
The synthesis of 5-MeO-7-TMT involves the modification of the tryptamine structure to introduce the methoxy and trimethyl groups. This process requires advanced knowledge of [[organic chemistry]] and access to specialized laboratory equipment.
As a tryptamine derivative, 5-MeO-7-TMT may produce effects similar to other compounds in this class, such as [[hallucinations]], [[euphoria]], and altered states of consciousness. However, due to limited research, the specific effects and safety profile of 5-MeO-7-TMT remain largely unknown.


==Related compounds==
=== Legal Status ===
* [[5-MeO-DMT]]
The legal status of 5-MeO-7-TMT varies by country. In some jurisdictions, it may be classified as a controlled substance due to its structural similarity to other psychoactive tryptamines. Researchers must be aware of local regulations when studying this compound.
* [[7-MeO-MiPT]]
* [[DMT]]
* [[Psilocybin]]


==See also==
== Related Pages ==
* [[List of tryptamines]]
* [[Psychedelic drug]]
 
==Related pages==
* [[Tryptamine]]
* [[Tryptamine]]
* [[Serotonin]]
* [[Serotonin]]
* [[Psychedelic therapy]]
* [[Psychoactive drug]]
* [[Hallucinogen]]
 
{{Psychedelics}}


[[Category:Tryptamines]]
[[Category:Tryptamines]]
[[Category:Psychedelic tryptamines]]
[[Category:Psychoactive drugs]]
[[Category:Serotonin receptor agonists]]

Latest revision as of 16:33, 16 February 2025

5-Methoxy-7,N,N-trimethyltryptamine[edit]

Chemical structure of 5-Methoxy-7,N,N-trimethyltryptamine

5-Methoxy-7,N,N-trimethyltryptamine (5-MeO-7-TMT) is a synthetic compound belonging to the class of tryptamines, which are structurally related to the naturally occurring neurotransmitter serotonin. This compound is of interest in the field of psychopharmacology due to its potential psychoactive effects.

Chemical Structure[edit]

5-MeO-7-TMT is a derivative of the tryptamine molecule, characterized by the presence of a methoxy group at the 5-position and three methyl groups attached to the nitrogen atom at the 7-position. The chemical formula for 5-MeO-7-TMT is C14H20N2O.

Pharmacology[edit]

The pharmacological properties of 5-MeO-7-TMT are not well-documented, but it is believed to interact with the serotonin receptors in the brain, similar to other tryptamines. This interaction may result in altered perception, mood, and cognition, although specific effects and potency are not well-studied.

Synthesis[edit]

The synthesis of 5-MeO-7-TMT involves the modification of the tryptamine backbone. The process typically includes the introduction of a methoxy group at the 5-position and the methylation of the nitrogen atom. These chemical modifications are carried out using standard organic synthesis techniques.

Potential Effects[edit]

As a tryptamine derivative, 5-MeO-7-TMT may produce effects similar to other compounds in this class, such as hallucinations, euphoria, and altered states of consciousness. However, due to limited research, the specific effects and safety profile of 5-MeO-7-TMT remain largely unknown.

Legal Status[edit]

The legal status of 5-MeO-7-TMT varies by country. In some jurisdictions, it may be classified as a controlled substance due to its structural similarity to other psychoactive tryptamines. Researchers must be aware of local regulations when studying this compound.

Related Pages[edit]