2495-96-7

Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a building block for the synthesis of various drug molecules, particularly antibiotics and antiviral agents, due to its unique chemical structure and properties.
Used in Antibacterial Applications:
In the pharmaceutical industry, ETHYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a key component in the development of new treatments for bacterial infections, leveraging its potential to target and combat harmful bacteria.
Used in Antiviral Applications:
ETHYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is also used as a promising candidate for the development of new treatments for viral infections, given its potential to inhibit viral replication and reduce the severity of viral diseases.
Used in Healthcare:
ETHYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used for its potential antioxidant and anti-inflammatory properties, which can contribute to the prevention and treatment of various health conditions, enhancing overall well-being and quality of life.

Upstream product

• 76155-50-5 ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 64-17-5 ethanol 
• 7512-17-6 N-Acetyl-D-glucosamine 
• 3006-60-8 Acetic acid (2R,3R,4R,5S,6R)-2,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-4-yl ester 
• 3006-60-8 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose 
• 51533-00-7 2-acetylamino-3,4,6-triacetyl-2-deoxy-α-D-glucopyranosyl bromide 
• 10034-19-2 1,3,4,6-tetra-O-acetyl-2-amino-2-deoxy-α-D-glucopyranose hydrochloride 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 7512-17-6 2-acetamido-2-deoxy-D-glucose 

Relevant academic research and scientific papers

Chemo-enzymatic approach to access diastereopure α-substituted GlcNAc derivatives

The formation of diastereopure α-substituted GlcNAc derivatives in a simple and straightforward way is a challenging task. Herein, we report the chemical synthesis of diastereomeric α/β-substituted GlcNAc derivatives under non-anhydrous atmosphere using u

PRODUCTION METHOD OF ALKYL N-ACETYLGLUCOSAMINIDE

PROBLEM TO BE SOLVED: To provide a method for obtaining alkyl N-acetylglucosaminide that comprises few content of N-acetyl glucosamine as impurities, conveniently and efficiently with a low cost. SOLUTION: The invention provides a production method of alkyl N-acetylglucosaminide comprising a step of reducing the content of N-acetyl glucosamine by contacting a mixture of alkyl N-acetylglucosaminide and N-acetyl glucosamine with strongly basic anion exchange resin (where, alkyl means an alkyl group of carbon number 1-4). The invention relates to the production method of alkyl N-acetylglucosaminide which is a mixture of alkyl N-acetylglucosaminide and N-acetyl glucosamine obtained by reaction of N-acetyl glucosamine, chitin, or chitin oligosaccharide with alkyl alcohol under the presence of an acid, or transglycosidation of chitin or chitin oligosaccharide using an enzyme with N-acetylhexosaminidase activity in a mixed solution of alkyl alcohol and water. COPYRIGHT: (C)2016,JPOandINPIT

HELICOBACTER PYLORI BACTERIUM PROLIFERATION INHIBITOR

The present invention herein provides a proliferation inhibitor of H. pylori bacteria comprising a compound that can specifically inhibit the proliferation of H. pylori bacteria, which does not generate bacterium resistant, can be eaten, drunken or administrated safely for a long period of time, can be simply mass-manufactured and can be used for foods and beverages or pharmaceutical preparation. The proliferation inhibitor of H. pylori bacteria comprises an N-acetylglucosaminyl beta-linked monosaccharide derivative represented by the following chemical formula (1): ????????GlcNAc1-beta-O-Y?????(1) wherein Y is an alkyl group, an alkoxyl group, an alkenyl group, an alkynyl group, an aralkyl group, an aryl group, a heteroaryl group, a carboxyl group or an alkoxycarbonyl group.

Discovery of the chemical function of glycosidases: Design, synthesis, and evaluation of mass-differentiated carbohydrate libraries

Equation presented. Discovery of the catalytic chemical function of the many putative glycosidases coded in genomes currently relies on individual testing of possible substrates, usually as their p-nitrophenol conjugate. Herein, we present an alternative chemical proteomics approach using a synthetic mass-differentiated heat-stable substrate library with mass spectrometry readout. Library components do not serve as reaction inhibitors and both primary and secondary enzyme substrates can be delineated.