Welcome to LookChem.com Sign In|Join Free
  • or
Neu5Ac alpha(2-6)Gal beta(1-4)GlcNAc-beta-pNP, also known as 4-Nitrophenyl O-(N-acetyl-a-neuraminosyl)-(2-6)-b-D-galactopyranosyl-(1-4)-2-acetamido-2-deoxy-b-D-glucopyranoside, is a complex carbohydrate molecule that plays a significant role in various biological processes. It is a derivative of sialic acid, which is an essential component of many glycoproteins and glycolipids on the surface of cells. This molecule is particularly important for its ability to interact with viral pathogens, making it a crucial target for understanding and developing antiviral strategies.

501427-93-6

Post Buying Request

501427-93-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

501427-93-6 Usage

Uses

Used in Virology Research:
Neu5Ac alpha(2-6)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 crucial in understanding how viruses bind to host cells and initiate infection, which can lead to the development of antiviral drugs and vaccines.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Neu5Ac alpha(2-6)Gal beta(1-4)GlcNAc-beta-pNP is used as a key component in the development of drugs targeting viral infections. By studying the interaction between this molecule and viral pathogens, researchers can design drugs that interfere with the virus's ability to bind to host cells, thereby preventing infection and spread.
Used in Diagnostics:
Neu5Ac alpha(2-6)Gal beta(1-4)GlcNAc-beta-pNP can also be employed in the development of diagnostic tools for detecting viral infections. By measuring the binding affinity of this molecule to specific viruses, diagnostic tests can be created to identify and monitor viral infections in patients.
Used in Glycobiology Research:
In the field of glycobiology, Neu5Ac alpha(2-6)Gal beta(1-4)GlcNAc-beta-pNP serves as an important model compound for studying the structure and function of glycans, which are essential for various biological processes, including cell-cell communication, immune response, and pathogen recognition. Understanding the role of this molecule in these processes can provide insights into the development of new therapeutic strategies for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 501427-93-6 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 501427-93:
(8*5)+(7*0)+(6*1)+(5*4)+(4*2)+(3*7)+(2*9)+(1*3)=116
116 % 10 = 6
So 501427-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C31H45N3O21/c1-11(37)32-19-15(39)7-31(30(46)47,55-27(19)21(41)16(40)8-35)50-10-18-22(42)24(44)25(45)29(53-18)54-26-17(9-36)52-28(20(23(26)43)33-12(2)38)51-14-5-3-13(4-6-14)34(48)49/h3-6,15-29,35-36,39-45H,7-10H2,1-2H3,(H,32,37)(H,33,38)(H,46,47)/t15-,16-,17+,18+,19-,20+,21-,22+,23-,24+,25+,26-,27-,28-,29+,31-/m1/s1

501427-93-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Neu5Acα(2-6)Galβ(1-4)GlcNAc-β-pNP

1.2 Other means of identification

Product number -
Other names (2R,4R,5R,6R)-5-acetamido-2-[[(2S,3R,4S,5S,6S)-6-[(2S,3S,4R,5S,6S)-5-acetamido-4-hydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:501427-93-6 SDS

501427-93-6Downstream Products

501427-93-6Relevant 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 (2005)

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

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 501427-93-6