28590-40-1

Usage

Uses

Used in Pharmaceutical Industry:
7,4'-DI-O-METHYLERIODICTYOL is used as a pharmaceutical agent for its potential therapeutic effects. 7,4'-DI-O-METHYLERIODICTYOL may exhibit beneficial properties such as anti-inflammatory, antioxidant, or antimicrobial activities, making it a promising candidate for the development of new drugs or supplements.
Used in Cosmetic Industry:
In the cosmetic industry, 7,4'-DI-O-METHYLERIODICTYOL is used as an active ingredient for its potential skin health benefits. It may be incorporated into skincare products for its antioxidant, anti-aging, or skin-soothing properties, contributing to improved skin health and appearance.
Used in Nutraceutical Industry:
7,4'-DI-O-METHYLERIODICTYOL is used as a nutraceutical ingredient for its potential health-promoting properties. It may be added to dietary supplements or functional foods to provide consumers with additional health benefits, such as enhanced immune function or improved metabolic health.
Used in Agricultural Industry:
In the agricultural industry, 7,4'-DI-O-METHYLERIODICTYOL may be used as a natural pesticide or fungicide due to its potential antimicrobial properties. It could be incorporated into organic farming practices to help protect crops from pests and diseases without the use of synthetic chemicals.

InChI:InChI=1/C17H16O6/c1-21-10-6-12(19)17-13(20)8-15(23-16(17)7-10)9-3-4-14(22-2)11(18)5-9/h3-7,15,18-19H,8H2,1-2H3

Upstream product

• 520-33-2 (S)-2,3-dihydro-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-benzopyrone 
• 77-78-1 dimethyl sulfate 
• 520-26-3 hesperidin 
• 74-83-9 methyl bromide 
• 520-33-2 hesperetin 
• 74-88-4 methyl iodide 

Relevant academic research and scientific papers

A PERSICOGENIN 3'-GLUCOSIDE FROM THE STEM BARK OF PRUNUS AMYGDALUS

A new flavanone glycoside, persicogenin 3'-glucoside (5,3'-dihydroxy-7,4'-dimethoxyflavanone 3'-glucoside) has been characterized from the stem bark of Prunus amygdalus. - Key words: Prunus amygdalus; Rosaceae; stem bark; persicogenin 3'-glucoside; NOE; 2D HOMCOR spectra.

Efficient synthesis of flavanone glucuronides

The first efficient synthesis of flavanone glucuronides as potential human metabolites is described. The synthetic strategy is based on acetyl protection, followed by a combination of chemical and enzymatic deprotection steps. As an example, the method is

Synthesis and antimicrobial activity of 7-alkoxyhesperetin derivatives

Some new 7-alkoxyhesperetin derivatives, 7-methoxy-(c), 7-butoxy-(d), 7-octyloxy-(e), 7-decyloxy- (f), and 7-dodecyloxyhesperetin(g), were synthesized and confirmed by UV, IR, 1H NMR, and MS spectra data. The series of the synthesized compounds has been screened for their antibacterial activity in vitro and evaluated their structure-activity relationships. Substitution of the H with alkyl groups at C-7-OH led to significant change of their antibacterial activity. The antibacterial activity of 7-alkoxyhesperetin derivatives increased with the elongating of the length of aliphatic chain, and the maximum activity was reached at twelve carbon atoms. Compound f showed the highest antibacterial activity among all the compounds. Springer Science+Business Media, LLC 2010.