Interesting facts
Interesting Facts about 3,9,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol
This complex compound, known for its intricate structure and diverse biological activities, is a fascinating subject of study for chemists and pharmacologists alike. Here are some intriguing aspects of this unique molecule:
- Structural Complexity: The compound features a distinctive isoquinoline core, which is a fusion of two aromatic rings. This configuration contributes to its interesting chemical properties and biological activities.
- Biodiversity and Natural Sources: Compounds similar to this one are often found in various plant species, indicating a potential role in traditional medicine. The study of these natural sources has led to discoveries about their therapeutic potentials.
- Biological Activity: Research has suggested that similar isoquinoline-based compounds exhibit a range of pharmacological effects that could include anti-inflammatory, antitumor, and neuroprotective properties. This broad spectrum makes them valuable in medicinal chemistry.
- Potential Applications: Given its structural features, this compound could be investigated for applications in pharmaceuticals, especially in the development of new therapeutic agents aimed at treating neurological disorders and cancers.
- Synthetic Adaptability: The synthesis of such a complex structure poses interesting challenges but also opportunities to explore innovative organic synthesis techniques. Scientists continually seek efficient pathways to produce these compounds, enhancing their availability for research.
In summary, 3,9,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol represents a blend of natural inspiration and synthetic ambition. Its diverse properties warrant further exploration, making it a subject of significant interest in the field of chemistry.
Synonyms
(+/-)-Isocorypalmine
Isocorypalmine, DL-
(R,S)-Isocorypalmine
DL-Tetrahydrocolumbamine
Isocorypalmine, (+/-)-
(R,S)-Tetrahydrocolumbamine
Isocorypalmine DL-form [MI]
6487-33-8
UNII-YHT108XMMM
YHT108XMMM
(+/-)-Alkaloid L from corydalis
3,9,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol
CHEMBL3780481
6H-Dibenzo(a,g)quinolizin-2-ol, 5,8,13,13a-tetrahydro-3,9,10-trimethoxy-
(+-)-Isocorypalmine
SCHEMBL680031
3,9,10-trimethoxyberbin-2-ol
CHEBI:140671
BDBM50152836
5,8,13,13-Tetrahydro-3,9,10-trimethoxy-6H-dibenzo(a,q)quinolizin-2-ol
6H-Dibenzo(a,q)quinolizin-2-ol, 5,8,13,13a-tetrahydro-3,9,10-trimethoxy-
AKOS032947778
6989-84-0
Q27294528
Solubility of 3,9,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol
The solubility of 3,9,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol can be quite fascinating, as it is influenced by various factors including its molecular structure and environmental conditions. Generally, compounds with multiple methoxy groups tend to show enhanced solubility in organic solvents, especially in polar solvents.
In the context of practical applications, understanding and predicting the solubility of this compound is essential for processes such as drug formulation. As a general remark, one could assert that:
In summary, while the precise solubility of 3,9,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol may require empirical testing for specific solvents, an understanding of its methoxy functionalities suggests a favorable solubility profile in suitable polar environments.