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

Benzyl 2-Benzyl-4,6-O-benzylidene-3-O-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-D-glucopyranosyl)-D-mannopyranoside is a vital tool in glycobiology research due to its ability to serve as a glycosyl donor in synthetic glycosylation reactions. This chemical features a benzylidene-protected glycosyl moiety, which allows for selective glycosylation at the anomeric position, resulting in the production of glycoconjugates with defined stereochemistry. Additionally, the presence of the acetamido and acetyl groups enhances the compound′s stability and solubility, making it suitable for various biochemical assays and enzymatic reactions. Researchers commonly utilize Benzyl 2-Benzyl-4,6-O-benzylidene-3-O-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-D-glucopyranosyl)-D-mannopyranoside in the synthesis of glycoconjugates, glycoproteins, and glycan arrays for studying glycan-protein interactions, carbohydrate-mediated biological processes, and host-pathogen interactions. Furthermore, 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 and cell signaling pathways. Overall, Benzyl 2-Benzyl-4,6-O-benzylidene-3-O-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-D-glucopyranosyl)-D-mannopyranoside plays a crucial role in advancing our understanding of glycobiology and contributes to the development of glycan-based diagnostics.