CAS 76015-42-4
:4H-1-Benzopyran-4-one,5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-methoxy-
Description:
The chemical substance known as 4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-methoxy- is a flavonoid derivative, characterized by its complex polyphenolic structure. It features a chromone backbone, which is a fused benzopyran system, and is substituted with multiple hydroxyl and methoxy groups that contribute to its potential biological activities. The presence of these functional groups often enhances the compound's antioxidant properties and may influence its interaction with various biological targets. This compound is of interest in pharmacology and natural product chemistry due to its potential therapeutic effects, including anti-inflammatory, anticancer, and neuroprotective activities. Its solubility and stability can vary based on the pH and solvent conditions, which are important for its application in research and potential medicinal use. Additionally, the compound's CAS number, 76015-42-4, allows for easy identification and reference in scientific literature and databases.
Formula:C18H16O8
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Found 7 products.
5,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-methoxy-4H-chromen-4-one
CAS:Formula:C18H16O8Purity:95%Color and Shape:SolidMolecular weight:360.31486-Methoxytricin
CAS:<p>6-Methoxytricin, isolated from Artemisia absinthium, is an inhibitor of AR, inhibits AKT activity, and can be used in diabetes research.</p>Formula:C18H16O8Purity:99.4%Color and Shape:SolidMolecular weight:360.315,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-methoxy-4H-chromen-4-one
CAS:5,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-methoxy-4H-chromen-4-onePurity:98%Molecular weight:360.32g/mol6-methoxytricin
CAS:Oxygen-heterocyclic compoundFormula:C18H16O8Purity:≥ 90.0 % (HPLC)Molecular weight:360.316-Methoxytricin
CAS:<p>6-Methoxytricin is a flavonoid derivative, which is primarily found in certain plant species, notably within the Asteraceae family. This compound is a secondary metabolite, synthesized in plants as part of their defense mechanisms. Its mode of action involves modulation of key signaling pathways, exhibiting notable anti-inflammatory and antioxidant activities. By inhibiting enzymes like cyclooxygenase (COX) and lipoxygenase (LOX), 6-Methoxytricin reduces the production of pro-inflammatory mediators. Additionally, its antioxidant properties stem from its ability to scavenge free radicals, thereby preventing oxidative stress-induced cellular damage.</p>Formula:C18H16O8Purity:Min. 95%Molecular weight:360.3 g/mol






