80930-74-1 Usage
Uses
Used in Pharmaceutical Industry:
3β-[(2-O-β-D-Glucopyranosyl-β-D-glucopyranuronosyl)oxy]oleana-12-ene-28-oic acid is used as a therapeutic agent for its anti-inflammatory properties, making it a potential treatment for various inflammation-related conditions.
Used in Oncology:
In the field of oncology, 3β-[(2-O-β-D-Glucopyranosyl-β-D-glucopyranuronosyl)oxy]oleana-12-ene-28-oic acid is used as an anti-cancer agent, targeting the reduction of tumor growth and potentially contributing to cancer treatment.
Used in Diabetes Management:
3β-[(2-O-β-D-Glucopyranosyl-β-D-glucopyranuronosyl)oxy]oleana-12-ene-28-oic acid is used as a potential treatment for diabetes, due to its ability to improve glucose metabolism and insulin sensitivity.
Used in Liver Health:
3β-[(2-O-β-D-Glucopyranosyl-β-D-glucopyranuronosyl)oxy]oleana-12-ene-28-oic acid is used in the context of liver health to support the organ's function and potentially treat liver-related diseases, given its hepatoprotective properties.
Used in Anti-hyperlipidemic Therapy:
3β-[(2-O-β-D-Glucopyranosyl-β-D-glucopyranuronosyl)oxy]oleana-12-ene-28-oic acid is utilized as an anti-hyperlipidemic agent to help manage and reduce high lipid levels in the blood, thus contributing to cardiovascular health.
Check Digit Verification of cas no
The CAS Registry Mumber 80930-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,3 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80930-74:
(7*8)+(6*0)+(5*9)+(4*3)+(3*0)+(2*7)+(1*4)=131
131 % 10 = 1
So 80930-74-1 is a valid CAS Registry Number.
80930-74-1Relevant academic research and scientific papers
SELECTIVE CLEAVAGE OF ESTER TYPE GLYCOSIDE-LINKAGES AND ITS APPLICATION TO STRUCTURE DETERMINATION OF NATURAL OLIGOGLYCOSIDES
Ohtani, Kazuhiro,Mizutani, Kenji,Ryoji, Kasai,Tanaka, Osamu
, p. 4537 - 4540 (2007/10/02)
On treatment with anhydrous LiI, 2,6-lutidine and anhydrous methanol, an ester type glycosyl linkage of acidic tri- and di-terpenes was selectively cleaved without decomposition of a reducing terminal of the resulting sugar moiety to give an anomeric mixture of methyl glycosides along with an aglycone or a pro-aglycone in quantitative yield.In this reaction, no hydrolysis of any other glycoside linkages took place.
