CAS 54377-24-1

7-Hydroxy-5,8-dimethoxyflavanone

Description:

7-Hydroxy-5,8-dimethoxyflavanone, with the CAS number 54377-24-1, is a flavonoid compound characterized by its flavanone structure, which includes a chromone backbone. This compound features hydroxyl and methoxy functional groups that contribute to its chemical properties and biological activities. The presence of the hydroxyl group at the 7-position enhances its potential for antioxidant activity, while the methoxy groups at the 5 and 8 positions can influence its solubility and reactivity. Flavonoids, including this compound, are known for their various health benefits, including anti-inflammatory, antimicrobial, and anticancer properties. 7-Hydroxy-5,8-dimethoxyflavanone may be found in certain plants and is of interest in pharmacological research due to its potential therapeutic applications. Its stability, solubility, and reactivity can vary depending on environmental conditions, making it a subject of study in both natural product chemistry and medicinal chemistry.

7-Hydroxy-5,8-dimethoxyflavane

CAS: 54377-24-1

Formula: C₁₇H₁₆O₅

Purity: 97.5%

Molecular weight: 300.3059

Ref: IN-DA00DGXR

7-Hydroxy-5,8-dimethoxyflavanone

CAS: 54377-24-1

7-Hydroxy-5,8-dimethoxyflavanone is a natural product of Chloranthus, Chloranthaceae.

Formula: C₁₇H₁₆O₅

Purity: 98%

Color and Shape: Solid

Molecular weight: 300.31

Ref: TM-TN3232

7-Hydroxy-5,8-dimethoxyflavanone

CAS: 54377-24-1

Formula: C₁₇H₁₆O₅

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 300.31

Ref: BP-SBP01307

7-Hydroxy-5,8-dimethoxyflavanone

CAS: 54377-24-1

7-Hydroxy-5,8-dimethoxyflavanone is a naturally occurring flavanone, which is a subcategory of flavonoids commonly found in various plants. This compound is derived from plant sources, often isolated during phytochemical studies examining the secondary metabolites produced by flora. The mode of action of 7-Hydroxy-5,8-dimethoxyflavanone involves modulating various biochemical pathways, potentially influencing enzymatic activity and signal transduction mechanisms. This flavanone has garnered scientific interest due to its reported bioactive properties, such as antioxidant and anti-inflammatory effects.

Uses and applications of 7-Hydroxy-5,8-dimethoxyflavanone are primarily in research settings, where it is utilized to explore its potential therapeutic benefits. Scientists investigate its efficacy in cell culture and animal models to better understand its effects on human health. Research is ongoing to assess its potential applications in developing nutraceuticals or pharmaceuticals, particularly in areas concerning oxidative stress and inflammation-related disorders. The exploration of its pharmacokinetic properties, safety profile, and bioavailability remains an active area of scientific inquiry.

Formula: C₁₇H₁₆O₅

Purity: Min. 95%

Molecular weight: 300.3 g/mol

Ref: 3D-ECA37724