70786-48-0

Usage

Uses

Used in Pharmaceutical Industry:
5-hydroxy-3,7-dimethoxy-2-phenyl-4H-chromen-4-one is used as a therapeutic agent for its antioxidant, anti-inflammatory, and potential anticancer properties. It is employed to reduce oxidative stress and inflammation in the body, as well as to inhibit the growth of cancer cells.
Used in Cardiovascular Health Applications:
5-hydroxy-3,7-dimethoxy-2-phenyl-4H-chromen-4-one is used as a cardiovascular health supplement for its ability to reduce cholesterol levels and improve blood vessel function, contributing to overall cardiovascular health.
Used in Cognitive Function and Neuroprotection Applications:
5-hydroxy-3,7-dimethoxy-2-phenyl-4H-chromen-4-one is used as a cognitive enhancer and neuroprotective agent for its potential to improve cognitive function and provide neuroprotection, making it a compound of interest for potential therapeutic applications in the field of neurology and mental health.

Upstream product

• 67-56-1 methanol 
• 548-83-4 galangin 
• 124-41-4 sodium methylate 
• 74-88-4 methyl iodide 
• 532-32-1 sodium benzoate 
• 17874-42-9 2'-hydroxy-2,4',6'-trimethoxyacetophenone 
• 93-97-0 benzoic acid anhydride 
• 6665-74-3 5,7-dihydroxy-3-methoxyflavone 
• 77-78-1 dimethyl sulfate 
• 55317-02-7 2-methoxy-1-(2,4,6-trihydroxyphenyl)ethanone 
• 500-99-2 3,5-dimethoxyphenol 
• 1385652-08-3 1-(2-hydroxy-4,6-dimethoxy-phenyl)-2-methoxy-3-phenyl-1,3-propanedione 
• 1385651-92-2 C₁₈H₁₈O₆ 
• 26964-29-4 3,5,7-trimethoxyflavone 

Downstream Products

• 147437-73-8 5-acetoxy-3,7-dimethoxyflavone 
• 26964-29-4 3,5,7-trimethoxyflavone 
• 480-14-8 isalpinin 
• 33803-31-5 5,8-dihydroxy-3,7-dimethoxyflavone 
• 1227479-70-0 5-hydroxy-3,7-dimethoxyflavanone 
• 33910-27-9 5,8-diacetoxy-3,7-dimethoxy-2-phenyl-chromen-4-one 
• 103450-99-3 3,5,7,8-tetramethoxyflavone 
• 20950-52-1 3,7-dimethoxy-2-(3',4'-methylenedioxy-phenyl)chromen-4-one 
• 40451-44-3 platanetin 
• 74693-69-9 3,5,7,8-tetrahydroxyflavone 

Relevant academic research and scientific papers

Synthesis of some commonly occurring 2-phenyl-4H-1-benzopyran-4-ones: Revised structures for three natural products

5-Hydroxy-6,7-dimethoxyflavone, 5-hydroxy-7,8-dimethoxyflavone, 5-hydroxy-3,7-dimethoxyflavone, 3-hydroxy-5,7-dimethoxyflavone, 5-hydroxy-7,8-dimethoxyisoflavone and 5,7-dihydroxy-3-methoxyflavone and their derivatives have been synthesised to confirm the

Synthesis of Platanetin - A Naturally Occuring Prenylated Flavone

Platanetin (3,5,7,8-tetrahydroxy-6-C-prenylflavone) (I) has been synthesized by the prenylation of 8-hydroxygalangin. 8-Hydroxygalangin has been synthesized by a new route.

O-methylation of flavonoids by cell-free extracts of calamondin orange

Cell-free extracts of calamondin orange (Citrus mitis) catalysed the O-methylation of almost all hydroxyls of a number of flavonoids, indicating the existence in citrus tissues of ortho, meta, para and 3-O-methyltransferases. The latter, hitherto unreported enzyme, catalysed the formation of 3-O-methyl ethers of galangin and quercetin. The stepwise O-methylation of a number of compounds, especially quercetin and quercetagetin, tends to suggest a coordinated sequence of O-methylations on the surface of a multienzyme complex. The methyl acceptor abilities of the flavonoid substrates used are discussed in relation to their hydroxyl substitution patterns and their negative electron density distribution.