86327-84-6

Usage

Chemical Properties

White Solid

InChI:InChI=1/C36H43NO15/c1-19(38)37-28-31(52-36-33(48-23(5)42)32(47-22(4)41)30(46-21(3)40)26(50-36)17-43-20(2)39)29-27(18-45-34(51-29)25-14-10-7-11-15-25)49-35(28)44-16-24-12-8-6-9-13-24/h6-15,26-36H,16-18H2,1-5H3,(H,37,38)/t26?,27?,28-,29-,30-,31+,32-,33-,34?,35-,36-/m0/s1

Upstream product

• 3554-93-6 benzyl 2-acetamido-2-deoxy-α-D-galactopyranoside 
• 72-87-7 N-acetyl-D-galactosamine 
• 100-51-6 benzyl alcohol 
• 3554-91-4 Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-galactopyranoside 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 

Downstream Products

• 90754-57-7 benzyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1<*>3)-2-acetamido-2-deoxy-α-D-galactopyranoside 
• 3809-10-7 benzyl (2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1→3)-2-acetamido-4,6-di-O-acetyl-2-deoxy-α-D-galactopyranoside 
• 86319-62-2 benzyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-di-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-galactopyranoside 
• 86319-63-3 benzyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-di-O-β-D-galactopyranosyl-α-D-galactopyranoside 
• 135874-85-0 Acetic acid (2R,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3R,4R,5S,6R)-3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-trifluoromethanesulfonyloxy-tetrahydro-pyran-4-yloxy)-tetrahydro-pyran-3-yl ester 
• 135874-86-1 benzyl 2-acetamido-4-O-benzoyl-6-O-benzyl-2-deoxy-3-O-(2,3,4,6,tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranoside 
• 86781-98-8 benzyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranoside 

Relevant academic research and scientific papers

Structural analysis of a family 101 glycoside hydrolase in complex with carbohydrates reveals insights into its mechanism

O-Linked glycosylation is one of the most abundant posttranslational modifications of proteins. Within the secretory pathway of higher eukaryotes, the core of these glycans is frequently an N-acetylgalactosamine residue that is α-linked to serine or threo

A PRACTICAL SYNTHESIS OF 2-ACETAMIDO-2-DEOXY-3,4-DI-O-β-D-GALACTOPYRANOSYL-D-GALACTOPYRANOSE

Two different sugar derivatives having free hydroxyl groups have been employed for synthesis of the title trisacharide.In one attempt, benzyl 2-acetamido-6-O-benzyl-2-deoxy-α-D-galactopyranoside (8) was treated with an excess of 2,3,4,6-tetra-O-acetyl-α-D