529-39-5 Usage
Description
SAKURANIN is a flavanone glycoside, specifically sakuranetin attached to a beta-D-glucopyranosyl residue at position 5 through a glycosidic linkage. It is a naturally occurring compound found in various plants and has been studied for its potential biological activities.
Uses
Used in Pharmaceutical Industry:
SAKURANIN is used as a bioactive compound for its potential therapeutic applications. SAKURANIN has been investigated for its various pharmacological properties, such as anti-inflammatory, antioxidant, and anticancer activities. Its presence in plants makes it a promising candidate for the development of novel drugs and treatments.
Used in Cosmetic Industry:
SAKURANIN is used as an ingredient in the cosmetic industry due to its antioxidant and anti-inflammatory properties. It can be incorporated into skincare products to provide potential benefits for skin health and protection against environmental stressors.
Used in Traditional Medicine:
SAKURANIN, being a natural compound, is also used in traditional medicine for its potential therapeutic effects. It may be utilized in the formulation of herbal remedies and supplements to support overall health and well-being.
Used in Research and Development:
SAKURANIN serves as a valuable compound for research and development in the field of biochemistry and pharmacology. Its unique structure and potential biological activities make it an interesting subject for further investigation, with the aim of discovering new applications and understanding its mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 529-39-5 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 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 529-39:
(5*5)+(4*2)+(3*9)+(2*3)+(1*9)=75
75 % 10 = 5
So 529-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H24O10/c1-29-12-6-15-18(13(25)8-14(30-15)10-2-4-11(24)5-3-10)16(7-12)31-22-21(28)20(27)19(26)17(9-23)32-22/h2-7,14,17,19-24,26-28H,8-9H2,1H3/t14-,17+,19+,20-,21+,22+/m0/s1
529-39-5Relevant articles and documents
FLAVONOID 5-GLUCOSIDES FROM PRUNUS CERASUS BARK AND THEIR CHARACTERISTIC WEAK GLYCOSIDIC BONDING
Geibel, Martin,Feucht, Walter
, p. 1519 - 1521 (2007/10/02)
Pinostrobin 5-glucoside, a novel flavanone glycoside, was isolated from the bark of Prunus cerasus.As it was not found in P. avium, the substance is useful to distinguish these two species.Apigenin 5-glucoside, genkwanin 5-glucoside and neosakuranin were also isolated from the bark of P. cerasus.They occur in both species as minor components.These 5-glucosides together with genistein 5-glucoside, prunetin 5-glucoside, sakuranin, tectochrysin 5-glucoside and luteolin 5-glucoside were hydrolysed in malic acid.The isoflavone and flavone 5-glucosides were shown to be hydrolysed more rapidly than the flavanone 5-glucosides, whereas no hydrolysis was observed with the corresponding 7-glucosides under the same conditions.The chalcone 2'-glucoside neosakuranin was transformed at first to the corresponding flavanone 5-glucoside, which was hydrolysed thereafter. Key Word Index - Prunus cerasus; Prunus avium; Rosaceae; bark; pinostrobin 5-glucoside; flavonoid 5-glucosides; hydrolysis.
