Azatadine
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- Molecular formula
- C20H24Cl2N2O
- CAS Number
- 3964-81-2
- IUPAC Name
- 3-[(2,4-dichloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-11-yl)oxy]-N,N-dimethyl-propan-1-amine
- Molecular Weight
- 325.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2700g/cm3
- Synonyms
- 18833-64-2
Identification
Interesting facts
Interesting Facts about 3-[(2,4-dichloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-11-yl)oxy]-N,N-dimethyl-propan-1-amine
This remarkable compound, a derivative of quinoline, features a unique molecular structure that exhibits a range of interesting properties. Here are some captivating insights into this compound:
- Pharmacological Potential: The compound is extensively studied for its potential therapeutic applications, particularly in the field of neuroscience. Its structure allows it to interact with various neurotransmitter systems, offering promise in treating conditions like depression and anxiety.
- Chlorine Atoms: The presence of chlorine atoms in its structure not only enhances its biological activity but also contributes to its lipophilicity, which affects how the compound interacts within biological systems.
- Cyclic Structure: The cycloheptamine moiety introduces a rigid conformation that may influence how the compound interacts with its target receptors, making it an intriguing subject for medicinal chemistry research.
- Dimethylamino Group: The N,N-dimethylamino functional group can increase the molecule's basicity, potentially impacting its pharmacodynamics and pharmacokinetics, which are critical factors in drug design.
- Research Implications: Ongoing studies may focus on the modification of this compound to enhance selectivity and reduce side effects, a common strategy in medicinal chemistry.
As scientists explore the myriad interactions of this compound, they continue to delve deeper into its mechanisms of action and potential for clinical applications. The fascinating interplay between its structure and biological effects highlights the importance of chemical diversity in the development of new therapeutic agents.