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2'-O-Galloylhyperin is a flavonoid compound derived from the combination of gallic acid and a hyperin molecule. It is known for its diverse pharmacological activities, such as antioxidant, anti-inflammatory, and anticancer properties. 2'-O-GALLOYLHYPERIN has been studied for its potential therapeutic effects on various conditions, including diabetes, cardiovascular diseases, and neurodegenerative disorders. Furthermore, 2'-O-galloylhyperin has demonstrated inhibitory effects on enzymes associated with disease progression, positioning it as a promising candidate for the development of new pharmaceuticals. As a natural remedy, 2'-O-galloylhyperin holds promise for addressing a range of health conditions, with ongoing research aimed at elucidating its mechanisms and potential applications.

53209-27-1

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53209-27-1 Usage

Uses

Used in Pharmaceutical Development:
2'-O-Galloylhyperin is used as a pharmaceutical candidate for its diverse pharmacological activities, including its antioxidant, anti-inflammatory, and anticancer properties. Its potential therapeutic effects on conditions such as diabetes, cardiovascular diseases, and neurodegenerative disorders make it a valuable asset in the development of new medications.
Used in Antioxidant Applications:
In the health and wellness industry, 2'-O-galloylhyperin is used as an antioxidant agent to combat oxidative stress and protect cells from damage. Its antioxidant properties contribute to the maintenance of overall health and the prevention of various diseases.
Used in Anti-Inflammatory Applications:
2'-O-Galloylhyperin is utilized as an anti-inflammatory agent in the treatment of inflammatory conditions. Its ability to reduce inflammation can help alleviate symptoms and improve the quality of life for individuals suffering from such conditions.
Used in Anticancer Applications:
In oncology, 2'-O-galloylhyperin is employed as an anticancer agent, targeting the inhibition of enzymes involved in disease progression. Its potential to synergize with conventional chemotherapeutic drugs enhances its efficacy in combating cancer cells and improving treatment outcomes.
Used in Enzyme Inhibition:
2'-O-Galloylhyperin is used as an enzyme inhibitor in various industries, including pharmaceuticals and biotechnology, to target specific enzymes associated with disease progression. Its inhibitory effects can contribute to the development of novel therapeutic strategies for the treatment of various conditions.
Overall, 2'-O-galloylhyperin's multifaceted applications across different industries highlight its potential as a versatile compound with significant implications for human health and disease management. Further research is essential to fully understand its mechanisms and maximize its potential in various fields.

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.

53209-27-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-2,3-dihydroxy-4-(hydroxymethyl)cyclohexyl] 3,5-dihydroxy-4-methoxybenzoate

1.2 Other means of identification

Product number -
Other names 2'-O-(2-METHOXYETHYL)CYTIDINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53209-27-1 SDS

53209-27-1Upstream product

53209-27-1Relevant academic research and scientific papers

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.

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