501427-92-5 Usage
Uses
Used in Virology Research:
Neu5Ac alpha(2-3)Gal beta(1-4)GlcNAc-beta-pNP is used as a substrate for determining the recognition specificity of viruses for receptor sugar chains. This application is essential in understanding how viruses interact with host cells and can help in the development of antiviral drugs and vaccines.
Used in Glycobiology and Glycochemistry:
In the field of glycobiology and glycochemistry, Neu5Ac alpha(2-3)Gal beta(1-4)GlcNAc-beta-pNP serves as a valuable tool for studying the structure and function of glycans, which are essential components of many biological molecules. This molecule can be used to investigate the enzymes responsible for glycan synthesis and processing, as well as their role in various cellular processes.
Used in Drug Development:
Neu5Ac alpha(2-3)Gal beta(1-4)GlcNAc-beta-pNP can be employed in the development of drugs targeting glycan-related diseases, such as cancer, inflammation, and infectious diseases. By understanding the specific interactions between viruses and their host cells, researchers can design drugs that interfere with these interactions, potentially leading to novel therapeutic strategies.
Used in Diagnostics:
This molecule can also be utilized in the development of diagnostic tools for detecting and monitoring viral infections. By measuring the binding affinity of viruses to Neu5Ac alpha(2-3)Gal beta(1-4)GlcNAc-beta-pNP, researchers can gain insights into the viral tropism and pathogenesis, which can aid in the early detection and treatment of infections.
Check Digit Verification of cas no
The CAS Registry Mumber 501427-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,4,2 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 501427-92:
(8*5)+(7*0)+(6*1)+(5*4)+(4*2)+(3*7)+(2*9)+(1*2)=115
115 % 10 = 5
So 501427-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C31H45N3O21/c1-11(38)32-19-15(40)7-31(30(46)47,54-26(19)21(42)16(41)8-35)55-27-22(43)17(9-36)51-29(24(27)45)53-25-18(10-37)52-28(20(23(25)44)33-12(2)39)50-14-5-3-13(4-6-14)34(48)49/h3-6,15-29,35-37,40-45H,7-10H2,1-2H3,(H,32,38)(H,33,39)(H,46,47)/t15-,16-,17+,18+,19-,20+,21-,22+,23-,24+,25-,26-,27+,28-,29+,31+/m1/s1
501427-92-5Relevant academic research and scientific papers
Convenient enzymatic synthesis of a p-nitrophenyl oligosaccharide series of sialyl N-acetyllactosamine, sialyl Lex and relevant compounds
Zeng, Xiaoxiong,Uzawa, Hirotaka
, p. 2469 - 2475 (2007/10/03)
From the β-d-Gal-(1→4)-β-d-GlcNAc-OC6H 4NO2-p (1) prepared by the transglycosylation of β-galactosidase from Bacillus circulans, α-d-Neu5Ac-(2→3)- β-d-Gal-(1→4)-β-d-GlcNAc-OC6H4NO 2-p (9) a
