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N-acetylneuraminyl-(2-3)-galactose is a chemical structure that plays a crucial role in biological processes, particularly in the glycosylation of glycoconjugates such as glycoproteins and glycolipids. This chemical is a type of sialic acid, which is a nine-carbon monosaccharide that often acts as a terminal component of sugar chains on the surface of cells and in secretions. The linkage of the N-acetylneuraminyl residue to the galactose molecule at position 2-3 is important for the recognition and binding of glycoproteins to other molecules, including other cells, pathogens, and extracellular matrix components. Additionally, this chemical structure is involved in various physiological and pathological processes, including cell signaling, immune response, and disease progression. Understanding the role and function of N-acetylneuraminyl-(2-3)-galactose is essential for elucidating its impact on human health and disease.

83563-61-5

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83563-61-5 Usage

Uses

Used in Pharmaceutical Industry:
N-acetylneuraminyl-(2-3)-galactose is used as a therapeutic agent for the development of drugs targeting various diseases, including cancer and infectious diseases. Its role in cell signaling and immune response makes it a promising candidate for modulating these processes and developing novel therapeutic strategies.
Used in Diagnostic Industry:
N-acetylneuraminyl-(2-3)-galactose is used as a diagnostic marker for detecting and monitoring various diseases, including cancer and infectious diseases. Its involvement in the recognition and binding of glycoproteins to other molecules makes it a valuable tool for identifying disease-specific changes in glycosylation patterns.
Used in Research Industry:
N-acetylneuraminyl-(2-3)-galactose is used as a research tool for studying the role and function of glycosylation in biological processes, including cell signaling, immune response, and disease progression. Its unique chemical structure and biological properties make it an important molecule for understanding the mechanisms underlying various physiological and pathological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 83563-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,6 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83563-61:
(7*8)+(6*3)+(5*5)+(4*6)+(3*3)+(2*6)+(1*1)=145
145 % 10 = 5
So 83563-61-5 is a valid CAS Registry Number.

83563-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-O-{(6R)-5-Amino-3,5-dideoxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]- β-L-threo-hex-2-ulopyranonosyl}-D-galactopyranose

1.2 Other means of identification

Product number -
Other names -

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:83563-61-5 SDS

83563-61-5Downstream Products

83563-61-5Relevant academic research and scientific papers

Two-Step Chemoenzymatic Detection of N-Acetylneuraminic Acid-α(2-3)-Galactose Glycans

Wen, Liuqing,Zheng, Yuan,Jiang, Kuan,Zhang, Mingzhen,Kondengaden, Shukkoor Muhammed,Li, Shanshan,Huang, Kenneth,Li, Jing,Song, Jing,Wang, Peng George

supporting information, p. 11473 - 11476 (2016/10/07)

Sialic acids are typically linked α(2-3) or α(2-6) to the galactose that located at the non-reducing terminal end of glycans, playing important but distinct roles in a variety of biological and pathological processes. However, details about their respective roles are still largely unknown due to the lack of an effective analytical technique. Herein, a two-step chemoenzymatic approach for the rapid and sensitive detection of N-acetylneuraminic acid-α(2-3)-galactose glycans is described.

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