5-Fluoro-α-methyltryptamine
- Molecular formula
- C12H15FN2
- CAS Number
- 52076-96-7
- IUPAC Name
- 2-(5-fluoro-1H-indol-3-yl)-2-methyl-propan-1-amine
- Molecular Weight
- 190.26g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2200g/cm3
- Synonyms
- INDOLE, 3-(2-AMINO-1, 1-DIMETHYLETHYL)-5-FLUORO-
Identification
Interesting Facts about 2-(5-Fluoro-1H-indol-3-yl)-2-methyl-propan-1-amine
The compound 2-(5-fluoro-1H-indol-3-yl)-2-methyl-propan-1-amine is a fascinating molecule that has garnered attention in various fields of research, particularly in medicinal chemistry and neuropharmacology.
Key Highlights
- Structural Diversity: This compound features a unique indole structure, which is a bicyclic structure comprised of a benzene ring fused to a pyrrole ring. Indole derivatives are known for their significant biological activities.
- Fluorination Effects: The presence of a fluorine atom in the indole moiety often influences the compound's biological properties, enhancing its potency and selectivity in binding to various receptors.
- Potential Therapeutic Uses: Compounds of this nature have been explored for their roles as potential therapeutic agents in treating mental health disorders, including depression and anxiety, thanks to their interactions with serotonin receptors.
- Research Interest: Studies have shown that similar structures can exhibit anti-cancer properties by modulating cellular pathways responsible for tumor growth.
Researchers are particularly interested in how the substitution pattern of the indole core affects pharmacological activity. As one expert noted, "Small changes in molecular structure can lead to significant shifts in biological activity." This highlights the importance of carefully designing and synthesizing compounds like 2-(5-fluoro-1H-indol-3-yl)-2-methyl-propan-1-amine to achieve desired effects in pharmacology.
Moreover, ongoing studies are focused on unraveling the mechanisms by which such compounds act at the molecular level, leading to insights that could pave the way for new therapeutic developments.