167875-39-0 Usage
Uses
Used in Pharmaceutical Industry:
Rubelloside B is used as a potential therapeutic agent for its ability to inhibit the growth of cancer cells, making it a candidate for cancer treatment. Its anti-inflammatory properties also contribute to its potential use in managing inflammatory conditions.
Used in Anti-diabetic Applications:
Rubelloside B is used as an anti-diabetic agent due to its demonstrated activity in managing blood sugar levels, which can be beneficial for the development of treatments for diabetes.
Used in Cardiovascular Applications:
Rubelloside B is used as a cardiovascular health promoter due to its beneficial effects on the cardiovascular system, which may include improving blood flow and reducing the risk of cardiovascular diseases.
Used in Drug Development:
Rubelloside B is used as a lead compound in the development of novel drugs for various diseases, leveraging its multifaceted therapeutic potential and natural origin for creating new pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 167875-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,8,7 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 167875-39:
(8*1)+(7*6)+(6*7)+(5*8)+(4*7)+(3*5)+(2*3)+(1*9)=190
190 % 10 = 0
So 167875-39-0 is a valid CAS Registry Number.
167875-39-0Relevant academic research and scientific papers
Fan, Gao-Jun,He, Zhi-Sheng
, p. 1139 - 1143 (1997)
From the roots of Adina rubella, four new quinovic acid glycosides, quinovic acid 3-O-β-D-glucopyranosyl(1→4)-β-D-fucopyranoside, quinovic acid 3-O-β-D-glucopyranosyl(1→4)-β-D-fucopyranosyl-(28→1)-β-D- glucopyranosyl ester, quinovic acid 3-O-β-D-glucopyranosyl(1→4)-α-L- rhamnopyranosyl-(28→1)-β-D-glucopyranosyl ester and quinovic acid 3-O-β- D-glucopyranosyl(1→2)-β-D-glucopyranosyl-(28→1)-β-D-glucopyranosyl ester, were isolated. Their structures were elucidated on the basis of hydrolytic and spectral methods.
