Benzyl 2-Acetamido-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranoside

Benzyl 2-Acetamido-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranoside is a compound extensively utilized in glycobiology research for its pivotal role in the synthesis of complex carbohydrates and glycoconjugates. Its mechanism of action involves serving as a glycosyl donor in glycosylation reactions, specifically facilitating the introduction of galactose residues into carbohydrate chains due to the presence of the galactopyranoside moiety. This compound is particularly valuable in the synthesis of galactose-containing oligosaccharides with precise regioselectivity and stereochemistry, achieved by strategically manipulating protecting groups such as benzyl and acetyl. Researchers harness its synthetic capabilities to construct diverse glycan structures, enabling investigations into carbohydrate-mediated processes such as cell-cell recognition, host-pathogen interactions, and immune responses. By employing Benzyl 2-Acetamido-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranoside, scientists can delve deeper into the roles of carbohydrates in biological systems, advancing our understanding of glycobiology and its implications in various research fields.