32748-59-7 Usage
Uses
Used in Pharmaceutical Industry:
2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosylsalicylate is used as a prodrug for aspirin to provide its therapeutic effects, such as pain relief, fever reduction, and anti-inflammatory action, while potentially minimizing gastrointestinal side effects. This makes it a candidate for patients who require long-term antiplatelet therapy but are at risk of gastrointestinal complications from traditional aspirin use.
Used in Anti-inflammatory Applications:
As a prodrug of aspirin, 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosylsalicylate is utilized for its anti-inflammatory properties, which can be beneficial in treating conditions characterized by inflammation, such as arthritis and other inflammatory disorders.
Used in Anti-cancer Research:
2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosylsalicylate is used in cancer research for its potential anti-cancer properties. It is being investigated for its ability to inhibit certain types of cancer cells, suggesting a possible role in cancer treatment or as an adjunct to existing therapies.
Used in Drug Development:
In the field of drug development, 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosylsalicylate serves as a subject of study to understand its pharmacokinetics, pharmacodynamics, and safety profile. This research is crucial for the development of new drugs that can offer the benefits of aspirin without the associated risks, particularly for patients with a history of gastrointestinal issues or other contraindications to traditional aspirin use.
Check Digit Verification of cas no
The CAS Registry Mumber 32748-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,4 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32748-59:
(7*3)+(6*2)+(5*7)+(4*4)+(3*8)+(2*5)+(1*9)=127
127 % 10 = 7
So 32748-59-7 is a valid CAS Registry Number.
32748-59-7Relevant academic research and scientific papers
Novel stereoselective synthesis of glycosyl-1-O-acyl esters via peracetylglycosyl phosphorothioates, -selenoates and -dithioates as glycosyl donors
Borowiecka, Joanna,Michalska, Maria
, p. 858 - 862 (2007/10/03)
An efficient and highly β-stereoselective synthesis of glycosyl 1-O-acyl esters based on reaction of easily accessible glycosylthio-, seleno- and dithiophosphates 1-6 as glycosyl donors with carboxylic acids 7-13 as glycosyl acceptors in the presence of silver salts as activators is described.
