520-42-3 Usage
Description
Asebogenin, also known as 4'-methyl ether derivative of phloretin, is a member of the dihydrochalcone class. It is a naturally occurring compound with various biological activities and potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
Asebogenin is used as a pharmaceutical compound for its potential therapeutic effects. It has been found to possess various biological activities, such as anti-inflammatory, anti-viral, and anti-cancer properties. Its ability to modulate cellular signaling pathways and interact with biopolymers and macromolecules makes it a promising candidate for the development of new drugs and treatments.
Used in Cosmetic Industry:
In the cosmetic industry, asebogenin is used as an active ingredient for its potential skin benefits. It may be utilized in the development of skincare products that target anti-aging, skin brightening, and skin protection against environmental stressors.
Used in Food Industry:
Asebogenin may also find applications in the food industry, particularly in the development of functional foods and beverages. Its potential health benefits and biological activities could be harnessed to create products with added nutritional value and health-promoting properties.
Check Digit Verification of cas no
The CAS Registry Mumber 520-42-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 520-42:
(5*5)+(4*2)+(3*0)+(2*4)+(1*2)=43
43 % 10 = 3
So 520-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O5/c1-21-12-8-14(19)16(15(20)9-12)13(18)7-4-10-2-5-11(17)6-3-10/h2-3,5-6,8-9,17,19-20H,4,7H2,1H3
520-42-3Relevant articles and documents
Dihydrochalcones: Evaluation as novel radical scavenging antioxidants
Nakamura, Yoshimasa,Watanabe, Shigeo,Miyake, Nobuyuki,Kohno, Hiroyuki,Osawa, Toshihiko
, p. 3309 - 3312 (2007/10/03)
Dihydrochalcones are a family of bicyclic flavonoids, defined by the presence of two benzene rings joined by a saturated three carbon bridge. In the present study, we systematically examined the antioxidant activities of dihydrochalcones against the stable free radical (1,1-diphenyl-2-picrylhydrazyl) and lipid peroxidation in the erythrocyte membrane. All dihydrochalcones exhibited higher antioxidant activities than the corresponding flavanones. The 1H NMR analysis indicated that the active dihydrochalcone has a time-averaged conformation in which the aromatic A ring is orthogonal to the carbonyl group, while the inactive dihydrochalcone such as 2′-O-methyl-phloretin has a strongly hydrogen-bonded phenolic hydroxyl group, suggestive of a coplanar conformation. A hydroxyl group at the 2′-position of the dihydrochalcone A ring, newly formed by reduction of the flavanone C ring, is an essential pharmacophore for its radical scavenging potential.
