131573-90-5 Usage
Uses
Used in Pharmaceutical Applications:
Camelliaside B is used as a therapeutic agent for its potential anti-inflammatory and anti-cancer properties. It helps in reducing inflammation and inhibiting the growth and progression of cancer cells.
Used in Nutraceutical Applications:
Camelliaside B is used as a dietary supplement for its antioxidant properties, which help protect the body from free radicals and support overall health.
Used in Cardiovascular Health Applications:
Camelliaside B is used as a cardiovascular health promoter, aiding in the regulation of blood sugar levels and improving heart health.
Used in Antimicrobial Applications:
Camelliaside B is used as an antimicrobial agent, exhibiting activity against various microorganisms and contributing to the prevention and treatment of infections.
Used in Neuroprotective Applications:
Camelliaside B is used as a neuroprotective agent, supporting the health and function of the nervous system and potentially reducing the risk of neurodegenerative diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 131573-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,5,7 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 131573-90:
(8*1)+(7*3)+(6*1)+(5*5)+(4*7)+(3*3)+(2*9)+(1*0)=115
115 % 10 = 5
So 131573-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C32H38O19/c1-10-19(38)23(42)25(44)31(46-10)49-27-21(40)17(8-33)48-32(29(27)51-30-24(43)20(39)15(37)9-45-30)50-28-22(41)18-14(36)6-13(35)7-16(18)47-26(28)11-2-4-12(34)5-3-11/h2-7,10,15,17,19-21,23-25,27,29-40,42-44H,8-9H2,1H3/t10-,15+,17+,19-,20-,21+,23+,24+,25+,27-,29+,30-,31-,32+/m0/s1
131573-90-5Relevant articles and documents
KAEMPFEROL GLYCOSIDES FROM HOSTA VENTRICOSA
Budzianowski, Jaromir
, p. 3643 - 3647 (2007/10/02)
Leaves of Hosta ventricosa yielded eight kaempferol glycosides, of which six: the 3-(2G-glucosylrutinoside)-7-glucoside, 3-sophoroside-7-glucoside, 3-rutinoside-7-glucoside, 3-(2G-glucosylrutinoside), 3-sophoroside, 3-rutinoside were fully characterized and two: 3-xylosylrutinoside-7-glucoside and 3-xylosylrutinoside were tentatively identified.Investigations included 1H-1H-COSY and 1H-1H 2D J NMR analysis.