1,3,4,6-Tetra-O-acetyl-2-(2′,3′,4′-tri-O-benzoyl-α-L-fucopyranosyl)-galactopyranose (CAS 141990-06-9)

1,3,4,6-Tetra-O-acetyl-2-(2′,3′,4′-tri-O-benzoyl-α-L-fucopyranosyl)-galactopyranose is a structurally complex carbohydrate derivative widely employed in glycobiology research. Its complex acetylation and benzoylation pattern mimic natural glycan motifs, making it a valuable tool for investigating carbohydrate-protein interactions and elucidating glycan-mediated biological processes. One significant research application of this compound lies in its use as a substrate for glycosyltransferases, enzymes involved in glycan biosynthesis. By serving as an acceptor substrate, this compound enables researchers to explore the substrate specificity and catalytic mechanisms of glycosyltransferases, contributing to our understanding of glycan assembly and modification pathways. Additionally, this derivative serves as a precursor for the synthesis of structurally diverse glycans and glycoconjugates with tailored properties. These synthetic glycans find utility in various research areas, including immunology, microbiology, and cancer biology, where they are utilized as probes for studying carbohydrate-mediated cellular recognition processes, host-pathogen interactions, and tumor-associated glycosylation patterns. Overall, 1,3,4,6-Tetra-O-acetyl-2-(2′,3′,4′-tri-O-benzoyl-α-L-fucopyranosyl)-galactopyranose plays a pivotal role in advancing our understanding of the biological functions and molecular mechanisms underlying glycan diversity and complexity.