2-[3-Hydroxy-4-(trideuteriomethoxy)phenyl]-5,6,7-trimethoxychromen-4-one is a synthetic organic compound belonging to the class of flavonoids, specifically a chromone derivative. This compound features a chromone backbone, which is characterized by a benzopyran structure, and is substituted with multiple methoxy groups and a hydroxyl group, contributing to its potential biological activity. The presence of the trideuteriomethoxy group indicates that it contains deuterium, which can be useful in studies involving isotopic labeling for tracing metabolic pathways or enhancing NMR spectroscopy analysis. The methoxy groups enhance the lipophilicity of the molecule, potentially influencing its solubility and bioavailability. This compound may exhibit various pharmacological properties, including antioxidant, anti-inflammatory, or anticancer activities, although specific biological effects would depend on further empirical studies. Its unique structure and isotopic labeling make it a valuable compound for research in medicinal chemistry and pharmacology.

2-[3-hydroxy-4-(trideuteriomethoxy)phenyl]-5,6,7-trimethoxychromen-4-one

1346599-39-0: 2-[3-Hydroxy-4-(trideuteriomethoxy)phenyl]-5,6,7-trimethoxychromen-4-one is a synthetic organic compound belonging to the class of flavonoids, specifically a chromone derivative. This compound features a chromone backbone, which is characterized by a benzopyran structure, and is substituted with multiple methoxy groups and a hydroxyl group, contributing to its potential biological activity. The presence of the trideuteriomethoxy group indicates that it contains deuterium, which can be useful in studies involving isotopic labeling for tracing metabolic pathways or enhancing NMR spectroscopy analysis. The methoxy groups enhance the lipophilicity of the molecule, potentially influencing its solubility and bioavailability. This compound may exhibit various pharmacological properties, including antioxidant, anti-inflammatory, or anticancer activities, although specific biological effects would depend on further empirical studies. Its unique structure and isotopic labeling make it a valuable compound for research in medicinal chemistry and pharmacology.

<p>Applications Labelled Eupatorin 5-Methyl Ether (E938850). Sinensetin, eupatorin, 3'-hydroxy-5,6,7,4'-tetramethoxyflavone and rosmarinic acid contents and antioxidative effect of Orthosiphon stamineus from Malaysia.<br>References Elliott, A., et al.: Biochem. Pharmacol., 44, 1603 (1992), Furuta, S., et al.: J. Food Sci., 62, 526 (1997),<br></p>

CAS 1346599-39-0

2-[3-hydroxy-4-(trideuteriomethoxy)phenyl]-5,6,7-trimethoxychromen-4-one

Eupatorin-d3 5-Methyl Ether

Ref: TR-E938852