Octyl Tetra-2,3,4,6-O-acetyl-β-D-thioglucopyranoside

Octyl Tetra-2,3,4,6-O-acetyl-β-D-thioglucopyranoside is a key compound utilized in biochemical and biophysical research, particularly in studies involving glycosylation and carbohydrate chemistry. This chemical features a glucopyranoside backbone with four acetyl groups and a thiol moiety, along with an octyl substituent. Its unique structure allows it to serve as a versatile tool for investigating glycosylation processes and interactions. Researchers often employ Octyl Tetra-2,3,4,6-O-acetyl-β-D-thioglucopyranoside as a substrate analog to study the activity and specificity of glycosyltransferases and glycosidases involved in glycoprotein and glycolipid biosynthesis. Additionally, its thiol group makes it suitable for conjugation reactions, enabling the synthesis of glycoconjugates and glycopeptides for structural and functional studies. Furthermore, this compound has been instrumental in developing glycosylation assays, screening platforms for glycosyltransferase inhibitors, and investigating the roles of glycosylation in various biological processes, including cell signaling, immune response, and host-pathogen interactions. Overall, Octyl Tetra-2,3,4,6-O-acetyl-β-D-thioglucopyranoside remains a crucial component in advancing our understanding of glycosylation mechanisms and their implications in cellular physiology and pathology.