Lisuride
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- Molecular formula
- C22H27N3O
- CAS Number
- 18016-80-3
- IUPAC Name
- 1,1-diethyl-3-(7-methyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea
- Molecular Weight
- 338.48g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2678g/cm3
- Synonyms
- Tergurid, Terguride, trans-Dihydrolisuride
Identification
Interesting facts
Interesting Facts about 1,1-Diethyl-3-(7-methyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea
This compound is a fascinating example of a complex organic structure that exemplifies the beautiful diversity found in the realm of chemical compounds. Here are some interesting aspects:
- Unique Structure: The compound incorporates an indole framework, known for its presence in many natural products and biological activities. Indoles often serve as the core structure in medicinally useful compounds.
- Pharmacological Potential: Compounds like this one are often investigated for their biological activity. Indol derivatives have been associated with numerous pharmacological properties, including anti-cancer, anti-inflammatory, and antimicrobial effects.
- Synthetic Importance: The synthesis of this compound may involve multiple steps, highlighting the intricate strategies chemists develop to construct complex molecules in the lab. Creating compounds with such detailed geometry and specific substituents is a true testament to synthetic organic chemistry.
- Research Applications: Due to its structural features, this compound is likely explored in research related to medicinal chemistry, possibly contributing to the development of novel therapeutic agents.
- Complexity in Design: The specific functional groups present indicate a design led by the goal of achieving particular interactions, whether by modifying solubility or targeting specific biological pathways.
In summary, 1,1-diethyl-3-(7-methyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea is a compound that embodies the intersection of organic chemistry, pharmacology, and therapeutic discovery, making it an exciting subject for further exploration.