Interesting facts
Interesting Facts about 2-(5-methoxy-1H-indol-3-yl)-N-methyl-ethanamine
2-(5-methoxy-1H-indol-3-yl)-N-methyl-ethanamine, often referred to as a derivative of the indole family, is a fascinating compound that has garnered attention in both academic research and pharmacological studies. Here are some intriguing points about this compound:
- Indole Derivative: This compound belongs to the indole class, which is notable for its role in various biological processes. Indoles are prevalent in many natural products and are known for their diverse pharmacological activities.
- Psychoactive Potential: Compounds in this class, including this one, have been studied for their psychoactive effects, particularly in relation to serotonin receptors. The structural similarity to known hallucinogens like psilocybin piques interest in its possible effects on the human psyche.
- Research Application: Specifically, researchers are investigating the role of N-methyl substitutions in enhancing the selectivity and potency of these compounds at receptor sites, potentially leading to novel therapeutic applications.
- Legal Status: The legality and regulation surrounding this compound can vary significantly by region. Understanding the legal implications is crucial for researchers working with psychoactive substances.
- Natural Occurrence: Many indole compounds are naturally occurring in plants and fungi, and this compound's methoxy group suggests it may have similar natural origins or effects.
In summary, 2-(5-methoxy-1H-indol-3-yl)-N-methyl-ethanamine stands out as a compound of great interest within the scientific community. Its unique properties and potential psychoactive effects provide ample opportunity for further exploration and understanding of human biology and the intricate functions of neurotransmitters.
As noted by researchers in the field, "The exploration of indole derivatives may unlock new pathways to understanding consciousness and mental health."
Synonyms
5-Methoxy-N-methyltryptamine
1H-Indole-3-ethanamine, 5-methoxy-N-methyl-
N,O-dimethylserotonin
YBO217L5YV
BRN 0160626
CHEBI:189635
N-METHYL-5-METHOXYTRYPTAMINE
5-MEO-NMT
UNII-YBO217L5YV
INDOLE, 5-METHOXY-3-(2-METHYLAMINO)ETHYL-
DTXSID40173909
Indole, 5-methoxy-3-[2-(methylamino)ethyl]-
5-22-12-00025 (Beilstein Handbook Reference)
INDOLE, 5-METHOXY-3-(2-(METHYLAMINO)ETHYL)-
DTXCID3096400
nfddcrihmzgwbp-uhfffaoysa-n
2009-03-2
2-(5-Methoxy-1H-indol-3-yl)-N-methylethanamine
5-methoxy-N-methyl-1H-indole-3-ethanamine
5-Methoxy NMT
n-methyl-5-methoxy-1h-indole-3-ethanamine
CHEMBL58579
5-methoxy-3-(2-methylamino)ethylindole
Oprea1_817351
SCHEMBL1130014
CAA00903
BDBM50038691
STK365327
AKOS005443520
HY-W721249
PD150636
DB-199536
2-(5-methoxy-1H-indol-3-yl)-ethyl-methyl-amine
[2-(5-Methoxy-1H-indol-3-yl)-ethyl]-methyl-amine
2-(5-Methoxy-1H-indol-3-yl)-N-methylethanamine #
Q4639626
Solubility of 2-(5-methoxy-1H-indol-3-yl)-N-methyl-ethanamine
The solubility of the compound 2-(5-methoxy-1H-indol-3-yl)-N-methyl-ethanamine in various solvents can be quite intriguing. Understanding its solubility characteristics is crucial for its applications in pharmaceutical and chemical industries.
Key points regarding its solubility include:
In summary, the solubility of this compound is likely to exhibit a moderate level of solubility in polar solvents while being less soluble in non-polar environments. As with many organic compounds, it is best to evaluate its solubility under specific conditions to fully understand its potential applications.