CAS 942609-65-6
:1,5,15-Tri-O-methylmorindol
Description:
1,5,15-Tri-O-methylmorindol is a chemical compound that belongs to the class of alkaloids, specifically derived from the morindol family. It is characterized by the presence of three methoxy (-OCH3) groups attached to the morindol structure, which significantly influences its solubility and reactivity. This compound is typically a white to off-white solid and is soluble in organic solvents such as methanol and ethanol, but less soluble in water due to its hydrophobic nature. The presence of methoxy groups enhances its biological activity, making it of interest in pharmacological research, particularly for its potential therapeutic properties. Additionally, 1,5,15-Tri-O-methylmorindol may exhibit antioxidant and anti-inflammatory activities, although specific biological effects can vary based on the context of use. Its molecular structure and functional groups contribute to its unique chemical behavior, making it a subject of study in organic chemistry and natural product research. As with many alkaloids, safety and handling precautions should be observed due to potential toxicity.
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
1,5,15-Tri-O-methylmorindol
CAS:<p>1,5,15-Tri-O-methylmorindol has effects against the Epstein-Barr virus early antigen (EBV-EA) activation induced by TPA.</p>Formula:C18H16O6Purity:98%Color and Shape:SolidMolecular weight:328.321,5,15-Tri-O-methylmorindol
CAS:Formula:C18H16O6Purity:95%~99%Color and Shape:Yellow powderMolecular weight:328.321,5,15-Tri-o-methylmorindol
CAS:<p>1,5,15-Tri-o-methylmorindol is a naturally occurring methylated indole derivative, which is a secondary metabolite isolated from certain plant species, particularly those in the Rubiaceae family. Its structure is characterized by the presence of multiple methyl groups, which are key to its unique chemical properties.</p>Formula:C18H16O6Purity:Min. 95%Molecular weight:328.3 g/mol
