23711-00-4 Usage
Description
4H-1-Benzopyran-4-one,5-(b-D-glucopyranosyloxy)-2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-, also known as Naringenin 5-β-D-Glucoside, is a flavanone natural product extracted from the willow bark of Salix species. It is a compound with a complex chemical structure, featuring a benzopyranone core with a glucopyranosyloxy group and multiple hydroxyl groups attached to the phenyl ring. This structure endows it with various biological activities and potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
4H-1-Benzopyran-4-one,5-(b-D-glucopyranosyloxy)-2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)is used as a pharmaceutical compound for its potential therapeutic effects. The compound has been found to possess antioxidant, anti-inflammatory, and anticancer properties, making it a promising candidate for the development of new drugs targeting various diseases, including cancer.
Used in Nutraceutical Industry:
In the nutraceutical industry, 4H-1-Benzopyran-4-one,5-(b-D-glucopyranosyloxy)-2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)is used as a natural ingredient in dietary supplements and functional foods. Its antioxidant and anti-inflammatory properties contribute to the overall health benefits of these products, promoting general well-being and supporting the immune system.
Used in Cosmetic Industry:
4H-1-Benzopyran-4-one,5-(b-D-glucopyranosyloxy)-2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)is used as an active ingredient in the cosmetic industry for its potential skin health benefits. The compound's antioxidant and anti-inflammatory properties can help protect the skin from environmental stressors, reduce inflammation, and promote a healthy, youthful appearance.
Used in Agricultural Industry:
In the agricultural industry, 4H-1-Benzopyran-4-one,5-(b-D-glucopyranosyloxy)-2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)can be used as a natural pesticide or growth promoter. Its antioxidant properties may help protect plants from stress and enhance their growth, while its anti-inflammatory effects could potentially reduce the incidence of plant diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 23711-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,1 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23711-00:
(7*2)+(6*3)+(5*7)+(4*1)+(3*1)+(2*0)+(1*0)=74
74 % 10 = 4
So 23711-00-4 is a valid CAS Registry Number.
23711-00-4Relevant articles and documents
Enzymatic Synthesis of Acylphloroglucinol 3-C-Glucosides from 2-O-Glucosides using a C-Glycosyltransferase from Mangifera indica
Chen, Dawei,Sun, Lili,Chen, Ridao,Xie, Kebo,Yang, Lin,Dai, Jungui
, p. 5873 - 5877 (2016)
A green and cost-effective process for the convenient synthesis of acylphloroglucinol 3-C-glucosides from 2-O-glucosides was exploited using a novel C-glycosyltransferase (MiCGTb) from Mangifera indica. Compared with previously characterized CGTs, MiCGTb exhibited unique de-O-glucosylation promiscuity and high regioselectivity toward structurally diverse 2-O-glucosides of acylphloroglucinol and achieved high yields of C-glucosides even with a catalytic amount of uridine 5′-diphosphate (UDP). These findings demonstrate for the first time the significant potential of a single-enzyme approach to the synthesis of bioactive C-glucosides from both natural and unnatural acylphloroglucinol 2-O-glucosides. One enzyme, one product: A novel C-glycosyltransferase from Mangifera indica is reported, which is a promiscuous catalyst that synthesizes bioactive C-glucosides from natural and unnatural acylphloroglucinol 2-O-gulcosides in one-pot reactions. High yields of C-glucosides were achieved even with a catalytic amount of uridine 5′-diphosphate. This study demonstrates for the first time the significant potential of a single-enzyme approach for the C-glycodiversification.
