Interesting facts
Interesting Facts about 3-(1-Methylpyrrolidin-3-yl)-1H-Indole
3-(1-Methylpyrrolidin-3-yl)-1H-indole represents a fascinating class of compounds known for their diverse applications in medicinal chemistry and pharmacology. Below are some engaging insights regarding this intriguing compound:
- Structural Innovation: The presence of the indole moiety, combined with a pyrrolidine ring, provides a unique structural foundation that can influence biological activity significantly.
- Biological Relevance: Indole derivatives are often found in nature and can act as crucial intermediates in the synthesis of various pharmaceuticals. The pyrrolidine part adds to its potential for creating novel therapeutic agents.
- Potential Activity: Compounds containing indole structures are widely studied due to their potential roles as anticancer agents, antidepressants, and anti-inflammatory drugs. Their ability to interact with various biological targets makes them compelling subjects of research.
- Research and Development: Many studies have shown that modifications to the indole backbone can lead to significant enhancements in efficacy and selectivity, thus making compounds like 3-(1-methylpyrrolidin-3-yl)-1H-indole crucial in drug design.
- Pharmacophore Modeling: The study of the pharmacophore—features of the molecule necessary to ensure interaction with biological macromolecules—gains from the distinct arrangement of atoms in this compound, aiding in predicting interactions.
- Versatile Synthesis: Researchers have developed various synthetic pathways to obtain compounds like this indole derivative, showcasing the versatility of organic synthesis techniques.
As a vivid example of the intersection between chemistry and biological sciences, 3-(1-methylpyrrolidin-3-yl)-1H-indole continues to be a promising area of research, ripe with possibilities for new discoveries and applications in drug development. Its unique structural characteristics facilitate a wide range of investigations into novel therapeutic avenues.
Synonyms
3671-00-9
INDOLE, 3-(1-METHYL-3-PYRROLIDINYL)-
3-(1-methylpyrrolidin-3-yl)-1H-indole
1H-Indole, 3-(1-methyl-3-pyrrolidinyl)-
MLS000736581
3-(1-Methyl-3-pyrrolidinyl)indole
NSC 43512
BRN 0912643
3-(1-Methyl-3-pyrrolidinyl)-1H-indole
NSC43512
SCHEMBL5253835
CHEMBL1340424
GIUCRWSFDBHBDT-UHFFFAOYSA-N
DTXSID601031949
NSC-43512
NCGC00246810-01
SMR000528205
Z1509146491
Solubility of 3-(1-methylpyrrolidin-3-yl)-1H-indole
The solubility of 3-(1-methylpyrrolidin-3-yl)-1H-indole can vary significantly based on several factors, particularly its interactions with solvents. Here are some key points to consider:
Interestingly, it is often said that "like dissolves like" – meaning compounds tend to dissolve better in solvents that share similar polarity. Thus, when looking to dissolve 3-(1-methylpyrrolidin-3-yl)-1H-indole, consider using an organic solvent such as ethanol or dimethyl sulfoxide (DMSO) for optimal results.
In conclusion, while the solubility behavior of this compound may not be extensively documented, understanding its chemical structure and potential solvent interactions can provide valuable insights into its solubility profile.