CAS 14585-04-7

5,7-DIHYDROXY-3,3',4',5'-TETRAMETHOXYFLAVONE

Description:

5,7-Dihydroxy-3,3',4',5'-tetramethoxyflavone, identified by its CAS number 14585-04-7, is a flavonoid compound characterized by its complex polyphenolic structure. This substance features multiple methoxy groups and hydroxyl groups, which contribute to its solubility and reactivity. The presence of these functional groups enhances its antioxidant properties, making it of interest in various biological and pharmaceutical applications. Flavonoids, including this compound, are known for their potential health benefits, including anti-inflammatory, anti-cancer, and cardioprotective effects. The specific arrangement of hydroxyl and methoxy groups in this flavone influences its biological activity and interaction with other molecules. Additionally, its structural characteristics may allow it to participate in various biochemical pathways, potentially impacting cellular processes. As with many flavonoids, it may also exhibit UV-absorbing properties, which can be beneficial in protecting against oxidative stress. Overall, 5,7-dihydroxy-3,3',4',5'-tetramethoxyflavone represents a significant compound within the realm of natural products and medicinal chemistry.

Formula: C₁₉H₁₈O₈

InChI: InChI=1/C19H18O8/c1-23-13-5-9(6-14(24-2)18(13)25-3)17-19(26-4)16(22)15-11(21)7-10(20)8-12(15)27-17/h5-8,20-21H,1-4H3

SMILES: COc1cc(cc(c1OC)OC)c1c(c(=O)c2c(cc(cc2o1)O)O)OC

Synonyms:

• Myricetin 3,3',4',5'-Tetramethyl Ether
• 5,7-dihydroxy-3-methoxy-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one
• 3,3',4',5'-Tetramethylmyricetin
• 5,7-DIHYDROXY-3,3',4',5'-TETRAMETHOXYFLAVONE
• Myricetin methylether
• 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-methoxy-2-(3,4,5-trimethoxyphenyl)-

4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-methoxy-2-(3,4,5-trimethoxyphenyl)-

CAS: 14585-04-7

Formula: C₁₉H₁₈O₈

Molecular weight: 374.3414

Ref: IN-DA001DGV

Myricetin methylether

CAS: 14585-04-7

Myricetin methylether is a flavonoid derivative, which is a naturally occurring compound structurally related to the primary flavonoid, myricetin. This compound is typically derived from plant sources, where myricetin and its derivatives are commonly found in various fruits, vegetables, and herbs. The primary mode of action of myricetin methylether involves its interaction with cellular oxidative processes and enzyme modulation, which can lead to a variety of biological effects, including antioxidant properties and enzyme inhibition.

Formula: C₁₉H₁₈O₈

Purity: Min. 95%

Color and Shape: Yellow Powder

Molecular weight: 374.34 g/mol

Ref: 3D-FM66084