4H-1-Benzopyran-4-one, 3,5,7,8-tetramethoxy-2-(3,4,5-trimethoxyphenyl)- - Names and Identifiers
Name | 3,5,7,8,3',4',5'-Heptamethoxyflavone
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Synonyms | Hibiscetin heptamethyl ether 3,5,7,8,3',4',5'-HEPTAMETHOXYFLA 3,5,7,8,3',4',5'-HeptaMethoxyflavone 3,3',4',5,5',7,8-Heptamethoxyflavone 3,5,7,8,3',4',5'-Heptamethoxyflavone 3',4',5',3,5,7,8-Heptamethoxyflavone 3,5,7,8-tetramethoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one 3,5,7,8-TetraMethoxy-2-(3,4,5-triMethoxyphenyl)-4H-chroMen-4-one 4H-1-Benzopyran-4-one, 3,5,7,8-tetramethoxy-2-(3,4,5-trimethoxyphenyl)-
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CAS | 21634-52-6
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4H-1-Benzopyran-4-one, 3,5,7,8-tetramethoxy-2-(3,4,5-trimethoxyphenyl)- - Physico-chemical Properties
Molecular Formula | C22H24O9
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Molar Mass | 432.42 |
Melting Point | 194-194.5℃ |
Storage Condition | 2-8°C |
4H-1-Benzopyran-4-one, 3,5,7,8-tetramethoxy-2-(3,4,5-trimethoxyphenyl)- - Reference
Reference Show more | 1. [IF=5.279] Linhua Huang et al."Effects of Scion/Rootstock Combination on Flavor Quality of Orange Juice from Huanglongbing (HLB)-Affected Trees: A Two-Year Study of the Targeted Metabolomics."J Agr Food Chem. 2020;68(10):3286–3296 2. [IF=3.701] Guijie Li et al."Protective effects of polymethoxyflavone-rich cold-pressed orange peel oil against ultraviolet B-induced photoaging on mouse skin."J Funct Foods. 2020 Apr;67:103834 |
4H-1-Benzopyran-4-one, 3,5,7,8-tetramethoxy-2-(3,4,5-trimethoxyphenyl)- - Introduction
3,5,7,8,3 ',4',5 '-Heptamethoxyflavone (3,5,7,8,3',4 ',5'-Heptamethoxyflavone) is a natural plant compound, it has the structure of flavonoids. It is a yellow crystalline solid with a distinctive odor.
This compound has a variety of biological activities, including antioxidant, anti-inflammatory, anti-cancer and other effects. It protects cells from oxidative stress by scavenging free radicals in the body, while also inhibiting inflammatory responses and tumor cell growth.
3,5,7,8,3 ',4',5 '-Heptamethoxyflavone has a wide range of applications in medical research and drug development. It can be used as a raw material for drugs or a template for drug development for the preparation of drugs with antioxidant, anti-inflammatory, anti-cancer and other functions.
The method of preparing 3,5,7,8,3 ',4',5 '-Heptamethoxyflavone is generally extracted from natural plants. First, plant material containing the compound, such as the peel of a citrus plant, is harvested. The target compound is then isolated from the plant material using solvent extraction techniques. Finally, pure 3,5,7,8,3 ',4',5 '-Heptamethoxyflavone was obtained by crystallization, purification and drying.
Regarding safety information, there is currently no clear report on 3,5,7,8,3 ',4',5 '-Heptamethoxyflavone. However, like other compounds, it is still necessary to pay attention to safe handling and follow relevant laboratory safety regulations. When using or handling the compound, wear appropriate personal protective equipment, such as gloves and protective glasses, to prevent contact with or inhalation of the compound.
Last Update:2024-04-09 21:01:54