
CAS 132923-24-1
:5-HYDROXY-7,2',3',4',5'-PENTAMETHOXYFLAVONE
Description:
5-Hydroxy-7,2',3',4',5'-pentamethoxyflavone is a flavonoid compound characterized by its multiple methoxy groups attached to the flavone backbone. This structure contributes to its potential biological activities, including antioxidant, anti-inflammatory, and anticancer properties. The presence of hydroxyl and methoxy groups enhances its solubility and reactivity, influencing its interaction with biological systems. The compound is typically studied for its pharmacological effects, particularly in the context of traditional medicine and natural products. Its CAS number, 132923-24-1, allows for precise identification in chemical databases. As a flavonoid, it may exhibit various mechanisms of action, including modulation of cell signaling pathways and inhibition of oxidative stress. Research into this compound is ongoing, focusing on its potential therapeutic applications and mechanisms of action in different biological contexts. Overall, 5-hydroxy-7,2',3',4',5'-pentamethoxyflavone represents a significant area of interest in phytochemistry and medicinal chemistry.
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Found 2 products.
5-Hydroxy-7-methoxy-2-(2,3,4,5-tetramethoxyphenyl)chromen-4-one
CAS:Formula:C20H20O8Molecular weight:388.3685-Hydroxy-7,2',3',4',5'-pentamethoxyflavone
CAS:<p>5-Hydroxy-7,2',3',4',5'-pentamethoxyflavone is a flavone that can be found in coffee. It has been shown to inhibit the enzyme arabinose isomerase and psiadiarabin, which are involved in the conversion of sugar into energy in plants. 5-Hydroxy-7,2',3',4',5'-pentamethoxyflavone also inhibits the plant enzyme phytase, which breaks down phytic acid. Phytic acid is a naturally occurring substance that binds to minerals such as calcium and zinc, preventing their absorption by the body. This compound has not shown any significant activity against bacterial DNA gyrase or topoisomerase IV or human DNA gyrase or topoisomerase II.</p>Formula:C20H20O8Purity:Min. 95%Molecular weight:388.37 g/mol

