N-[1-[2-(1H-indol-3-yl)ethyl]-4-piperidyl]benzamide
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- Molecular formula
- C22H25N3O
- CAS Number
- 144010-09-9
- IUPAC Name
- N-[1-[2-(1H-indol-3-yl)ethyl]-4-piperidyl]benzamide
- Molecular Weight
- 349.46g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2600g/cm3
- Synonyms
- INDORAMIN
Identification
Interesting facts
Interesting Facts about N-[1-[2-(1H-indol-3-yl)ethyl]-4-piperidyl]benzamide
N-[1-[2-(1H-indol-3-yl)ethyl]-4-piperidyl]benzamide is a fascinating compound that captures the interest of scientists across various fields due to its intriguing structure and potential applications. Below are some compelling aspects of this compound:
- Pharmacological Relevance: This compound has been studied for its potential use in neurological therapeutics. Its indole structure is particularly notable, as indoles are found in many biologically active compounds, including neurotransmitters.
- Structural Complexity: The presence of both indole and piperidine rings contributes to its structural diversity, making it a fascinating subject for studies in medicinal chemistry.
- Research Potential: Numerous studies aim to evaluate the compound's efficacy as a drug candidate, particularly in targeting specific receptors in the brain, which could lead to advancements in treating disorders such as depression or anxiety.
- Hybrid Architecture: The unique combination of the piperidine and benzamide moieties offers intriguing possibilities for modifying its pharmacophore, enhancing its activity or selectivity towards certain biological targets.
- Natural Compounds Inspiration: Indole derivatives like this compound often mimic structures found in nature, showcasing how natural products inspire synthetic chemistry and drug design.
In summary, N-[1-[2-(1H-indol-3-yl)ethyl]-4-piperidyl]benzamide stands out as a compound with significant potential in medicinal chemistry, driven by its unique structural characteristics and alignment with pharmacologically active frameworks. Its continuous exploration could pave the way for future therapeutic agents.