Benzyl 4-O-(2,3,4,6-Tetra-O-benzyl α-D-galactopyranosyl)-2,3-di-O-benzyl-6-O-benzoyl-β-D-galactopyranoside

Benzyl 4-O-(2,3,4,6-Tetra-O-benzyl α-D-galactopyranosyl)-2,3-di-O-benzyl-6-O-benzoyl-β-D-galactopyranoside plays a crucial role in glycobiology research, particularly in the synthesis of complex carbohydrates and glycoconjugates. Its mechanism of action involves serving as a glycosyl donor in glycosylation reactions, facilitating the formation of glycosidic bonds between carbohydrate moieties. This compound has been extensively utilized in the synthesis of structurally defined oligosaccharides for studying carbohydrate-protein interactions, cell surface recognition, and the modulation of carbohydrate-mediated biological processes. Additionally, it has been instrumental in the development of glycan microarrays, enabling high-throughput screening of carbohydrate-protein interactions and the profiling of glycan-binding proteins. Moreover, Benzyl 4-O-(2,3,4,6-Tetra-O-benzyl α-D-galactopyranosyl)-2,3-di-O-benzyl-6-O-benzoyl-β-D-galactopyranoside has been employed in the synthesis of neoglycoconjugates and glycodendrimers, contributing to the design of glycoclusters with tailored multivalency and spatial arrangements. These applications provide valuable insights into the molecular recognition of carbohydrates and their roles in various biological processes, advancing our understanding of glycoscience and its implications in biology and medicine.