Galanthamine hydrobromide
- Molecular formula
- C17H21NO3.HBr
- CAS Number
- 1953-04-4
- IUPAC Name
- 2-[(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-ium-1-yl)methyl]-3-ethyl-9,10-dimethoxy-4,6,7,11b-tetrahydro-1H-benzo[a]quinolizine;chloride
- Molecular Weight
- 368.87g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4300g/cm3
- Synonyms
- NS00126779
Identification
Interesting Facts about 2-[(6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-ium-1-yl)methyl]-3-ethyl-9,10-dimethoxy-4,6,7,11b-tetrahydro-1H-benzo[a]quinolizine; Chloride
This complex compound belongs to a class of chemicals known as isoquinolines, which have fascinating biological activities. Isoquinolines have been extensively studied for their potential in medicinal chemistry due to their ability to interact with various biological targets.
Key Highlights:
- Medicinal Potential: Compounds containing isoquinoline structures have shown promise in drug discovery and development, particularly in the treatment of neurological disorders.
- Bioactivity: The presence of methoxy groups in this compound suggests increased lipophilicity, which can enhance the compound's ability to penetrate biological membranes, potentially leading to higher bioactivity.
- Synthetic Routes: The synthesis of such complex molecules often involves multiple reaction steps, showcasing the ingenuity and creativity of organic chemists. Techniques such as stock's reaction or multicomponent reactions might be used in the synthetic pathway.
- Cationic Character: The quaternary ammonium nature of the isoquinoline contributes to its positive charge, which can influence the compound's reactivity and interaction with biological targets.
Scientists are constantly exploring the structural variations in isoquinoline derivatives to uncover new pharmacological applications. The versatility of this compound makes it a subject of great interest in both synthetic organic chemistry and medicinal research.
Moreover, the unique features of its structural components make it an exciting candidate for studies in molecular recognition and receptor binding, opening avenues for further research based on its interactions at the molecular level.