5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,8-dimethoxy-4H-chromen-4-one, also known by its CAS number 14965-08-3, is a flavonoid compound characterized by its complex polyphenolic structure. This substance features multiple hydroxyl (-OH) groups, which contribute to its potential antioxidant properties, making it of interest in various biological and pharmacological studies. The presence of methoxy (-OCH3) groups enhances its lipophilicity, potentially influencing its bioavailability and interaction with biological membranes. This compound is typically derived from natural sources, particularly plants, and may exhibit various biological activities, including anti-inflammatory, antimicrobial, and anticancer effects. Its structural features allow for interactions with various biological targets, which can be explored for therapeutic applications. Additionally, the compound's stability and solubility can vary based on environmental conditions, such as pH and temperature, which are important considerations in both laboratory and potential clinical settings. Overall, 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,8-dimethoxy-4H-chromen-4-one represents a significant area of interest in natural product chemistry and pharmacology.

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,8-dimethoxy-4H-chromen-4-one

14965-08-3: 5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,8-dimethoxy-4H-chromen-4-one, also known by its CAS number 14965-08-3, is a flavonoid compound characterized by its complex polyphenolic structure. This substance features multiple hydroxyl (-OH) groups, which contribute to its potential antioxidant properties, making it of interest in various biological and pharmacological studies. The presence of methoxy (-OCH3) groups enhances its lipophilicity, potentially influencing its bioavailability and interaction with biological membranes. This compound is typically derived from natural sources, particularly plants, and may exhibit various biological activities, including anti-inflammatory, antimicrobial, and anticancer effects. Its structural features allow for interactions with various biological targets, which can be explored for therapeutic applications. Additionally, the compound's stability and solubility can vary based on environmental conditions, such as pH and temperature, which are important considerations in both laboratory and potential clinical settings. Overall, 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,8-dimethoxy-4H-chromen-4-one represents a significant area of interest in natural product chemistry and pharmacology.

5,7,4'-Trihydroxy-3,8,3'-trimethoxyflavone is a natural product and can be used as a standard reference.

CAS 14965-08-3

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,8-dimethoxy-4H-chromen-4-one

5,7,4'-Trihydroxy-3,8,3'-trimethoxyflavone

Ref: TM-TN7314

Gossypetin 3,3',8-trimethylether

Ref: 5G-82553