105594-08-9 Usage
Description
(1S)-1,5-anhydro-2-O-(6-deoxy-alpha-L-mannopyranosyl)-1-[7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol is a complex chemical compound that features a unique combination of a sugar molecule, a flavonoid, and a glucitol moiety. The sugar molecule, 6-deoxy-alpha-L-mannopyranosyl, is glycosidically linked to the glucitol group, creating a distinctive sugar alcohol derivative. The flavonoid component, 7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl, contributes antioxidant and anti-inflammatory properties to the molecule. This intricate structure and its potential bioactive properties suggest that (1S)-1,5-anhydro-2-O-(6-deoxy-alpha-L-mannopyranosyl)-1-[7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol may find applications in various fields, including pharmaceuticals, nutraceuticals, and as a research tool in chemical biology.
Uses
Used in Pharmaceutical Industry:
(1S)-1,5-anhydro-2-O-(6-deoxy-alpha-L-mannopyranosyl)-1-[7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol is used as a potential therapeutic agent for various conditions due to its antioxidant and anti-inflammatory properties. The flavonoid component may contribute to the treatment or management of diseases where oxidative stress and inflammation play a significant role.
Used in Nutraceutical Industry:
In the nutraceutical sector, (1S)-1,5-anhydro-2-O-(6-deoxy-alpha-L-mannopyranosyl)-1-[7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol may be utilized as a dietary supplement or functional food ingredient. Its antioxidant and anti-inflammatory characteristics could provide health benefits when incorporated into consumer products aimed at promoting overall wellness and reducing the risk of certain diseases.
Used in Chemical Biology Research:
(1S)-1,5-anhydro-2-O-(6-deoxy-alpha-L-mannopyranosyl)-1-[7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol serves as a valuable research tool in chemical biology. Its unique structure allows scientists to study the interactions between different molecular components and their effects on biological systems. This can lead to a better understanding of molecular mechanisms and the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 105594-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,9 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105594-08:
(8*1)+(7*0)+(6*5)+(5*5)+(4*9)+(3*4)+(2*0)+(1*8)=119
119 % 10 = 9
So 105594-08-9 is a valid CAS Registry Number.