23246-80-2

Basic information

• Product Name: 5,7-Diacetoxy-8-methoxyflavone
• Synonyms: 5,7-Diacetoxy-8-methoxyflavone;5,7-Bis(acetyloxy)-8-methoxy-2-phenyl-4H-1-benzopyran-4-one;5,7-Dihydroxy-8-methoxyflavone diacetate;8-Methoxy-4-oxo-2-phenyl-4H-chromene-5,7-diyl diacetate
• CAS NO: 23246-80-2
• Molecular Formula: C₂₀H₁₆O₇
• Molecular Weight: 368.33684
• Mol File: 23246-80-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 5,7-Diacetoxy-8-methoxyflavone(CAS DataBase Reference)
• NIST Chemistry Reference: 5,7-Diacetoxy-8-methoxyflavone(23246-80-2)
• EPA Substance Registry System: 5,7-Diacetoxy-8-methoxyflavone(23246-80-2)

Safety Data

• Hazardous Substances Data: 23246-80-2(Hazardous Substances Data)

Usage

General Description

5,7-Diacetoxy-8-methoxyflavone is a flavonoid compound with chemical formula C19H16O7. It is a naturally occurring substance found in various plants, including Kaempferia parviflora and Strobilanthes cusia. This chemical has been studied for its potential biological activities, including anti-inflammatory, antioxidant, and anticancer properties. It has also been investigated for its potential use in traditional medicine for various health conditions, although further research is needed to fully understand its therapeutic potential and safety profile. Additionally, 5,7-Diacetoxy-8-methoxyflavone may have applications in the development of new pharmaceuticals and natural health products.

Upstream product

• 632-85-9 wogonin 
• 108-24-7 acetic anhydride 

Relevant articles and documents

Activities of Wogonin Analogs and Other Flavones against Flavobacterium columnare

In our on-going pursuit to discover natural products and natural product-based compounds to control the bacterial species Flavobacterium columnare, which causes columnaris disease in channel catfish (Ictalurus punctatus), we synthesized flavone and chalcone analogs, and evaluated these compounds, along with flavonoids from natural sources, for their antibacterial activities against two isolates of F. columnare (ALM-00-173 and BioMed) using a rapid bioassay. The flavonoids chrysin (1a), 5,7-dihydroxy-4′-methoxyflavone (11), isorhamnetin (26), luteolin (27), and biochanin A (29), and chalcone derivative 8b showed strong antibacterial activities against F. columnare ALM-00-173 based on minimum inhibition concentration (MIC) results. Flavonoids 1a, 8, 11, 13 (5,4′-dihydroxy-7-methoxyflavone), 26, and 29 exhibited strong antibacterial activities against F. columnare BioMed based upon MIC results. The 24-h 50% inhibition concentration (IC50) results revealed that 27 and 29 were the most active compounds against F. columnare ALM-00-173 (IC50 of 7.5 and 8.5 mg/l, resp.), while 26 and 29 were the most toxic compound against F. columnare BioMed (IC50 of 9.2 and 3.5 mg/l, resp.). These IC50 results were lower than those obtained for wogonin against F. columnare ALM-00-173 and F. columnare BioMed (28.4 and 5.4 mg/l, resp.). However, based on MIC results, none of the compounds evaluated in this study were as active as wogonin (MIC 0.3 mg/l for each F. columnare isolate). Further modification of the wogonin structure to enhance antibacterial is of interest.