Octyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside (CAS 173725-22-9)

Octyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside is a valuable compound used extensively in biochemical research, particularly in the study of glycosylation and carbohydrate chemistry. Its chemical structure consists of a glucopyranoside backbone with an acetamido group and three acetyl groups, along with an octyl substituent. This chemical has been employed in various research applications due to its ability to mimic glycosylated substrates and interact with glycosyltransferases and glycosidases. Specifically, it serves as a substrate analog for investigating the enzymatic activity and specificity of glycosyltransferases involved in the biosynthesis of glycoproteins and glycolipids. Furthermore, Octyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside has been utilized in the synthesis of oligosaccharides and glycoconjugates for structural and functional studies. Its hydrophobic octyl group also makes it suitable for incorporation into lipid bilayers, facilitating the investigation of membrane-associated glycosylation processes. Additionally, researchers have utilized this compound to develop glycosylation assays, high-throughput screening platforms for glycosyltransferase inhibitors, and to investigate the roles of glycosylation in various biological phenomena, such as cell signaling, immune response, and pathogen-host interactions. Overall, Octyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside continues to be an indispensable tool in advancing our understanding of glycosylation mechanisms and their implications in cellular processes.