Acetergamine: Difference between revisions

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{{Short description|A chemical compound used in research}}
== Acetergamine ==
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477318123
| IUPAC_name = (2S)-2-(1H-indol-3-yl)-N,N-dimethylethanamine
| image = Acetergamine.svg
| width = 200px
| CAS_number = 61-54-1
| PubChem = 6099
| ChemSpiderID = 5874
| UNII = 8NA5SWF92O
| ChEMBL = 1201247
| C=12
| H=16
| N=2
| smiles = CN(C)CCc1c[nH]c2c1cccc2
}}


'''Acetergamine''' is a chemical compound that belongs to the class of [[tryptamines]]. It is primarily used in scientific research and has been studied for its potential effects on the [[central nervous system]].
[[File:Acetergamine.svg|thumb|right|Chemical structure of Acetergamine]]


==Chemical Structure and Properties==
'''Acetergamine''' is a chemical compound that belongs to the class of [[ergoline]] derivatives. It is known for its pharmacological properties and potential therapeutic applications. Acetergamine is structurally related to other ergoline compounds, which are known for their effects on the [[central nervous system]].
Acetergamine is a derivative of [[tryptamine]], which is a naturally occurring monoamine alkaloid. The chemical structure of acetergamine includes an indole ring, which is a common feature in many biologically active compounds. The presence of the indole ring is significant as it is involved in the compound's interaction with various [[neurotransmitter]] receptors.


==Pharmacology==
== Chemical Structure ==
Acetergamine acts as an agonist at certain [[serotonin receptor]] subtypes, particularly the 5-HT<sub>2A</sub> receptor. This interaction is thought to be responsible for its psychoactive effects. The compound's ability to modulate serotonin receptors makes it a subject of interest in the study of [[psychedelic]] substances and their potential therapeutic applications.


==Research Applications==
Acetergamine is characterized by its complex [[ergoline]] ring system, which is a common feature among compounds in this class. The chemical structure of Acetergamine includes a tetracyclic ring system with various functional groups that contribute to its biological activity.
In research settings, acetergamine is used to study the effects of serotonin receptor activation. It serves as a tool for understanding the role of serotonin in mood regulation, perception, and cognition. Researchers also explore its potential use in developing treatments for [[mental health]] disorders such as [[depression]] and [[anxiety]].


==Safety and Legal Status==
== Pharmacology ==
As a research chemical, acetergamine is not approved for medical use in humans. Its legal status varies by country, and it is often regulated under laws pertaining to psychoactive substances. Researchers handling acetergamine must adhere to strict safety protocols to prevent accidental exposure.


==Related Compounds==
Acetergamine interacts with several [[neurotransmitter]] systems in the brain. It is known to act as an agonist at certain [[serotonin receptor|serotonin receptors]], which may account for some of its psychoactive effects. Additionally, Acetergamine may have affinity for [[dopamine receptor|dopamine receptors]], influencing mood and perception.
Acetergamine is structurally related to other tryptamines, such as [[serotonin]], [[melatonin]], and [[psilocybin]]. These compounds share a common indole structure and have varying effects on the central nervous system.


==Related pages==
== Potential Uses ==
* [[Tryptamine]]
* [[Serotonin]]
* [[Psychedelic drug]]
* [[Neurotransmitter]]


[[Category:Tryptamines]]
Research into Acetergamine has suggested potential applications in the treatment of certain [[neurological disorder|neurological disorders]]. Its ability to modulate neurotransmitter systems makes it a candidate for further study in conditions such as [[migraine]], [[Parkinson's disease]], and [[schizophrenia]].
[[Category:Research chemicals]]
 
[[Category:Serotonin receptor agonists]]
== Safety and Toxicity ==
 
As with many ergoline derivatives, the safety profile of Acetergamine is an important consideration. Studies on its toxicity and potential side effects are necessary to determine its suitability for therapeutic use. Common concerns with ergoline compounds include [[vasoconstriction]] and potential [[hallucinogenic]] effects.
 
== Related Pages ==
 
* [[Ergoline]]
* [[Serotonin receptor]]
* [[Dopamine receptor]]
* [[Neurological disorder]]
 
[[Category:Ergoline derivatives]]
[[Category:Pharmacology]]

Revision as of 21:24, 11 February 2025

Acetergamine

Chemical structure of Acetergamine

Acetergamine is a chemical compound that belongs to the class of ergoline derivatives. It is known for its pharmacological properties and potential therapeutic applications. Acetergamine is structurally related to other ergoline compounds, which are known for their effects on the central nervous system.

Chemical Structure

Acetergamine is characterized by its complex ergoline ring system, which is a common feature among compounds in this class. The chemical structure of Acetergamine includes a tetracyclic ring system with various functional groups that contribute to its biological activity.

Pharmacology

Acetergamine interacts with several neurotransmitter systems in the brain. It is known to act as an agonist at certain serotonin receptors, which may account for some of its psychoactive effects. Additionally, Acetergamine may have affinity for dopamine receptors, influencing mood and perception.

Potential Uses

Research into Acetergamine has suggested potential applications in the treatment of certain neurological disorders. Its ability to modulate neurotransmitter systems makes it a candidate for further study in conditions such as migraine, Parkinson's disease, and schizophrenia.

Safety and Toxicity

As with many ergoline derivatives, the safety profile of Acetergamine is an important consideration. Studies on its toxicity and potential side effects are necessary to determine its suitability for therapeutic use. Common concerns with ergoline compounds include vasoconstriction and potential hallucinogenic effects.

Related Pages