132498-72-7 Usage
Uses
Used in Biochemical Research:
4-Nitrophenyl2-acetamido-2-deoxy-3,6-di-O-benzoyl-b-D-galactopyranoside is used as a research tool for studying carbohydrate metabolism and enzyme activity. Its unique structure allows for the investigation of various biochemical processes and interactions.
Used as a Substrate in Enzymatic Assays:
In enzymatic assays, 4-Nitrophenyl2-acetamido-2-deoxy-3,6-di-O-benzoyl-b-D-galactopyranoside serves as a substrate to evaluate the activity of specific enzymes. Its cleavage by these enzymes can be monitored, providing insights into enzyme kinetics and mechanisms.
Used in Studying Glycosyltransferase Activity:
4-Nitrophenyl2-acetamido-2-deoxy-3,6-di-O-benzoyl-b-D-galactopyranoside is utilized to study the activity of glycosyltransferases, enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. 4-Nitrophenyl2-acetamido-2-deoxy-3,6-di-O-benzoyl-b-D-galactopyranoside's role in these studies aids in understanding the regulation and function of glycosylation in biological systems.
Used in Pharmaceutical Development:
Although not explicitly mentioned in the provided materials, given its relevance to carbohydrate metabolism and enzyme activity, 4-Nitrophenyl2-acetamido-2-deoxy-3,6-di-O-benzoyl-b-D-galactopyranoside could potentially be used in the development of pharmaceuticals targeting carbohydrate-related diseases or conditions, such as diabetes or certain genetic disorders affecting glycosylation pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 132498-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,9 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132498-72:
(8*1)+(7*3)+(6*2)+(5*4)+(4*9)+(3*8)+(2*7)+(1*2)=137
137 % 10 = 7
So 132498-72-7 is a valid CAS Registry Number.
132498-72-7Relevant academic research and scientific papers
Syntheses of the 3- and 4-thio analogues of 4-nitrophenyl 2-acetamido-2-deoxy-β-d-gluco- and galactopyranoside
Chen, Hong-Ming,Withers, Stephen G.
, p. 2212 - 2222 (2008/02/12)
The syntheses of 4-nitrophenyl β-glycosides of the 3-thio and 4-thio analogues of the two principal 2-acetamido-2-deoxy-hexoses found in living systems, GlcNAc and GalNAc, are described. While synthesis of the 4-thio analogues could be achieved via nucleophilic displacements of sulfonate derivatives with thioacetate, problems with neighbouring group acetamido participation necessitated the use of sulfamidate intermediates for the 3-thio analogues. These 3- and 4-thio analogues are employed in the chemo-enzymatic synthesis of thio-oligosaccharide analogues of structures present in glycosaminoglycans, glycoproteins and glycolipids.
