56316-75-7 Usage
Uses
Used in Pharmaceutical Industry:
4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)5,7-dihydroxy-3-[[6-O-(3,4,5-trihydroxybenzoyl)-α-D-glucopyranosyl]oxy]is used as a potential therapeutic agent for various conditions due to its antioxidant and anti-inflammatory properties. It may be particularly effective in treating cardiovascular diseases, cancer, and neurodegenerative disorders.
Used in Nutraceutical Industry:
4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)5,7-dihydroxy-3-[[6-O-(3,4,5-trihydroxybenzoyl)-α-D-glucopyranosyl]oxy]is used as a dietary supplement or functional food ingredient to support overall health and well-being. Its potential antioxidant and anti-inflammatory properties may contribute to improved immune function and reduced risk of chronic diseases.
Used in Cosmetic Industry:
4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)5,7-dihydroxy-3-[[6-O-(3,4,5-trihydroxybenzoyl)-α-D-glucopyranosyl]oxy]is used as an active ingredient in skincare products to promote skin health and protect against environmental stressors. Its antioxidant properties may help to reduce signs of aging and improve skin elasticity.
Used in Research and Development:
4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)5,7-dihydroxy-3-[[6-O-(3,4,5-trihydroxybenzoyl)-α-D-glucopyranosyl]oxy]is used as a subject of scientific research to further explore its pharmacological potential and mechanisms of action. This may lead to the development of new drugs and therapies for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 56316-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,1 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56316-75:
(7*5)+(6*6)+(5*3)+(4*1)+(3*6)+(2*7)+(1*5)=127
127 % 10 = 7
So 56316-75-7 is a valid CAS Registry Number.
56316-75-7Relevant academic research and scientific papers
Synthesis and antiradical activity of isoquercitrin esters with aromatic acids and their homologues
He?mánková-Vav?íková, Eva,K?enková, Alena,Petrásková, Lucie,Chambers, Christopher Steven,Zápal, Jakub,Kuzma, Marek,Valentová, Kate?ina,K?en, Vladimír
, (2017/05/25)
Isoquercitrin, (IQ, quercetin-3-O-β-D-glucopyranoside) is known for strong chemoprotectant activities. Acylation of flavonoid glucosides with carboxylic acids containing an aromatic ring brings entirely new properties to these compounds. Here, we describe
Effects of Functional Groups and Sugar Composition of Quercetin Derivatives on Their Radical Scavenging Properties
Kato, Komei,Ninomiya, Masayuki,Tanaka, Kaori,Koketsu, Mamoru
supporting information, p. 1808 - 1814 (2016/08/02)
Quercetin derivatives are widespread in the plant kingdom and exhibit various biological actions. The aim of this study was to investigate the structure-activity relationships of quercetin derivatives, with a focus on the influence of functional groups and sugar composition on their antioxidant capacity. A series of quercetin derivatives were therefore prepared and assessed for their DPPH radical scavenging properties. Isoquercetin O-gallates were more potent radical scavengers than quercetin. The systematic analysis highlights the importance of the distribution of hydroxy substituents in isoquercetin O-gallates to their potency.
