82209-72-1 Usage
Uses
Used in Pharmaceutical Industry:
14-deoxyandrographoside is used as a therapeutic agent for various health conditions due to its anti-inflammatory, hepatoprotective, and anti-tumor properties. It is particularly beneficial for conditions such as rheumatoid arthritis, liver diseases, and certain types of cancers.
Used in Nutraceutical Industry:
14-deoxyandrographoside is used as a dietary supplement to support immune function and overall health. Its ability to modulate immune responses and reduce oxidative stress makes it a valuable ingredient in nutraceutical products.
Used in Cosmetic Industry:
14-deoxyandrographoside is used as an active ingredient in skincare products for its anti-inflammatory and antioxidant properties. It may help reduce inflammation, promote skin healing, and protect against environmental stressors.
Further research is needed to fully understand the pharmacological effects and clinical applications of 14-deoxyandrographoside, as well as to explore its potential in other industries and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 82209-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82209-72:
(7*8)+(6*2)+(5*2)+(4*0)+(3*9)+(2*7)+(1*2)=121
121 % 10 = 1
So 82209-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C26H40O9/c1-14-4-7-18-25(2,16(14)6-5-15-9-11-33-23(15)32)10-8-19(28)26(18,3)13-34-24-22(31)21(30)20(29)17(12-27)35-24/h9,16-22,24,27-31H,1,4-8,10-13H2,2-3H3/t16?,17-,18+,19-,20-,21+,22-,24-,25+,26+/m1/s1
82209-72-1Relevant academic research and scientific papers
Li, Yuan,Lin, Hui-Xin,Wang, Jian,Yang, Jian,Lai, Chang-Jiang-Sheng,Wang, Xing,Ma, Bao-Wei,Tang, Jin-Fu,Li, Yong,Li, Xin-Lin,Guo, Juan,Gao, Wei,Huang, Lu-Qi
, p. 5999 - 6002 (2018)
ApUGT, a diterpene glycosyltransferase from Andrographis paniculata, could transfer a glucose to the C-19 hydroxyl moiety of andrograpanin to form neoandrographolide. This glycosyltransferase has a broad substrate scope, and it can glycosylate 26 natural and unnatural compounds of different structural types. This study provides a basis for exploring the glycosylation mechanism of ent-labdane-type diterpenes and plays an important role in diversifying the structures used in drug discovery.
