Benzyl 2-Benzyl-4,6-O-benzylidene-3-O-(2-acetamido-2-deoxy-D-glucopyranosyl)-D-mannopyranoside

Benzyl 2-Benzyl-4,6-O-benzylidene-3-O-(2-acetamido-2-deoxy-D-glucopyranosyl)-D-mannopyranoside is extensively utilized in glycobiology research for its role as a glycosyl donor in chemical and enzymatic glycosylation reactions. As a carbohydrate derivative, it serves as a valuable substrate for investigating glycosyltransferase-mediated processes and studying glycan-protein interactions. The chemical structure, featuring a benzylidene-protected glycosyl moiety, facilitates selective glycosylation at the anomeric position, yielding glycoconjugates with defined stereochemistry. Moreover, the presence of the acetamido group enhances the stability and solubility of the compound in aqueous environments, making it suitable for various biochemical assays and enzymatic reactions. Researchers commonly employ Benzyl 2-Benzyl-4,6-O-benzylidene-3-O-(2-acetamido-2-deoxy-D-glucopyranosyl)-D-mannopyranoside in the synthesis of glycoconjugates, glycoproteins, and glycan arrays for probing carbohydrate-mediated biological processes. Additionally, its compatibility with diverse glycosylation strategies and glycan-modifying enzymes enables the generation of structurally diverse glycan libraries, facilitating the elucidation of glycan recognition events, cell signaling pathways, and host-pathogen interactions. This compound′s versatility and utility in glycobiology research contribute to advancements in understanding the roles of carbohydrates in health and disease, as well as the development of novel glycan-based diagnostics.