53209-27-1 Usage
General Description
2'-O-Galloylhyperin is a chemical compound belonging to the class of flavonoids. It is derived from the Gallic acid and a hyperin molecule. 2'-O-GALLOYLHYPERIN has been found to possess various pharmacological activities, including antioxidant, anti-inflammatory, and anticancer properties. It has also been studied for its potential therapeutic effects on conditions such as diabetes, cardiovascular diseases, and neurodegenerative disorders. Additionally, 2'-O-galloylhyperin has been reported to exhibit inhibitory effects on enzymes involved in the progression of various diseases, making it a promising candidate for the development of new pharmaceuticals. Overall, this compound shows potential as a natural remedy for a range of health conditions, and further research is needed to fully understand its mechanisms and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 53209-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,0 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53209-27:
(7*5)+(6*3)+(5*2)+(4*0)+(3*9)+(2*2)+(1*7)=101
101 % 10 = 1
So 53209-27-1 is a valid CAS Registry Number.
53209-27-1Relevant articles and documents
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.
