
CAS 97914-19-7
:3,4'-Dihydroxy-3',5,7-trimethoxyflavan
Description:
3,4'-Dihydroxy-3',5,7-trimethoxyflavan, identified by its CAS number 97914-19-7, is a flavonoid compound characterized by its polyphenolic structure, which contributes to its antioxidant properties. This compound features multiple hydroxyl (-OH) groups and methoxy (-OCH3) substituents, which enhance its solubility and reactivity. The presence of these functional groups allows it to participate in various biochemical interactions, potentially offering health benefits such as anti-inflammatory and anti-cancer effects. Its flavonoid backbone is known for contributing to the stability of the molecule and its ability to scavenge free radicals. Additionally, 3,4'-Dihydroxy-3',5,7-trimethoxyflavan may exhibit biological activities that can influence cellular signaling pathways. This compound is of interest in pharmacological research and may be studied for its potential applications in nutraceuticals and therapeutic agents. Overall, its unique structural features and biological activities make it a subject of interest in both natural product chemistry and medicinal research.
Formula:C18H20O6
Synonyms:- (2R,3R)-2-(4-hydroxy-3-methoxyphenyl)-5,7-dimethoxychroman-3-ol
- 3,4'-Dihydroxy-3',5,7-trimethoxyflavan
- 3,4'-DIHYDROXY-3',5,7-TRIMETHOXY
- 2-(4-Hydroxy-3-Methoxyphenyl)-5,7-diMethoxychroMan-3-ol
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Found 5 products.
5,7,3'-Tri-O-methyl (-)-epicatechin
CAS:<p>5,7,3'-Tri-O-methyl (-)-epicatechin</p>Purity:98%Molecular weight:332.35g/mol3,4'-Dihydroxy-3,5',7-trimethoxyflavan
CAS:3,4'-Dihydroxy-3,5',7-trimethoxyflavan is a flavonoid compound extracted from the stem of Machilus japonica and is a phospholipase C71 (PLCγ1) inhibitor.Formula:C18H20O6Purity:98%Color and Shape:SolidMolecular weight:332.353,4'-Dihydroxy-3',5,7-trimethoxyflavan
CAS:Formula:C18H20O6Purity:95%~99%Color and Shape:PowderMolecular weight:332.3523,4'-Dihydroxy-3,5',7-trimethoxyflavan
CAS:<p>3,4'-Dihydroxy-3,5',7-trimethoxyflavan is a natural flavonoid compound, which is a type of polyphenolic molecule. This compound is predominantly derived from various plant sources where it often functions as a secondary metabolite. The mode of action of 3,4'-Dihydroxy-3,5',7-trimethoxyflavan primarily involves its antioxidant properties. It acts by scavenging free radicals and reducing oxidative stress at a cellular level, which may contribute to its potential therapeutic effects.</p>Formula:C18H20O6Purity:Min. 95%Molecular weight:332.3 g/mol





