146288-30-4

Usage

Uses

Used in Pharmaceutical Research:
AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a key intermediate in the synthesis of pharmaceutical compounds for drug development. Its unique structure allows for the creation of new molecules with potential therapeutic properties.
Used in Biochemical Research:
In the field of biochemical research, AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a building block for the synthesis of bioactive compounds. Its acetylated form facilitates easier handling and manipulation in laboratory settings, making it an important molecule for studying carbohydrate chemistry and its role in biological processes.
Used in Drug Development:
AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is employed as a precursor in the development of new drugs. Its structural modifications provide a foundation for the design of innovative pharmaceutical agents with potential applications in treating various diseases and conditions.
Used in Carbohydrate Chemistry Studies:
In the study of carbohydrate chemistry, AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used to explore the interactions between carbohydrates and other biomolecules. Its unique structure offers insights into the role of carbohydrates in biological processes and their potential applications in medicine and biotechnology.
Used in Synthesis of Bioactive Compounds:
AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a starting material for the synthesis of bioactive compounds with potential applications in various industries, including pharmaceuticals, cosmetics, and food science. Its versatility and stability make it an attractive candidate for the development of novel compounds with therapeutic or functional properties.

Upstream product

• 71-41-0 pentan-1-ol 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose 
• 3006-60-8 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose 
• 3068-34-6 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranosyl chloride 
• 146288-29-1 Pentyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 108-24-7 acetic anhydride 

Downstream Products

• 94483-64-4 Pentyl 2-acetamido-2-deoxy-β-D-glucopyranoside 

Relevant academic research and scientific papers

Convergent synthesis of tetra- and penta-saccharide fragments of dimeric Lewis X

The convergent synthesis of tetra- and penta-saccharide fragments of the TACA dimeric Lex is described. The synthetic strategy relied on the preparation of a protected GlcNTCA-(1,3)-Gal-(1,4)-GlcNAc trisaccharide diol free at O-3 of both glucos

N-ACETYLGLUCOSAMINE DERIVATIVES AND USE THEREOF

The present invention relates to An N-acetylglucosamine derivative represented by the following formula (1), and a hyaluronic acid production promoting agent containing the same and a skin external preparation containing the same: wherein R1 is a hydrogen atom or an alkyl group having 2 to 18 carbon atoms; R2, R3, and R4 are hydrogen atoms or acyl groups having 2 to 18 carbon atoms and may be all the same or different from others; the steric structure at position 1 may be α or β; provided that R1, R2, R3, and R4 must not be all hydrogen atoms. It is intended to provide an easily available hyaluronic acid production promoting agent and a skin external preparation whereby the production of hyaluronic acid can be promoted in the skin and thus the skin can be maintained in a vital and moist state so that it is expected that the human skin can be prevented from age.

Use of sodium iodide and crown ether in the synthesis of N-acetylglucosamine glycosides

A pair of sodium iodide-crown ether reagents was used in the synthesis of N-acetylglucosamine glycosides. At room temperature, the reaction resulted in β-glycosides, whereas at 85-90°C, it gave a mixture of anomers or α-anomer only.

Process for the specific synthesis of β-glycosidically linked N-acetylpyranoside derivatives

A process for the stereospecific synthesis of β-glycosidically linked N-acetylglucosamine derivatives is provided, wherein a protected α-(N-acetyl-2-amino-2-deoxy)-β-pyranosyl halide is coupled to a glycosyl acceptor using zinc chloride and a 4,4'-dialkox

A spacer-modified disaccharide as a photoaffinity reagent for the acceptor-binding area of bovine (1->4)-β-D-galactosyltransferase: comparison of its acceptor properties with those of other 2-acetamido-2-deoxy-β-D-glucopyranosides

The spacer-modified disaccharide 1,10-di-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2-azi-1,10-decanediol (10) that mimics the biantennary core heptasaccharide of N-glycoproteins has been synthesised.Compound 10 is an excellent acceptor in galactosyltransferase-catalysed galactosylation by UDP-galactose, is superior (7-8 fold) to analogues that have only one GlcNAc unit, and is an efficient photoaffinity reagent for galactosyltransferase.In the presence of UDP-Gal, no photoaffinity labelling by 10 takes place, which agrees with the mechanism of galactosyltransferase action.