Phenyl N-Benzyl-2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-1-thio-beta-D-glucopyranoside (CAS 910805-49-1)

Phenyl N-Benzyl-2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-1-thio-beta-D-glucopyranoside, a synthetic compound, has emerged as a pivotal tool in glycobiology research, offering insights into glycan-mediated processes and molecular interactions. Its structural features enable precise manipulation of glycan moieties, facilitating the investigation of glycan-protein recognition events. Researchers have employed Phenyl N-Benzyl-2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-1-thio-beta-D-glucopyranoside to explain glycan-dependent cellular signaling pathways and host-pathogen interactions. Through glycan engineering approaches, this compound has been instrumental in deciphering the roles of specific glycans in cellular adhesion, migration, and immune responses. Furthermore, its ability to modulate glycan structures allows for the interrogation of glycosylation patterns and their impact on cellular physiology. Studies have demonstrated the utility of Phenyl N-Benzyl-2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-1-thio-beta-D-glucopyranoside in probing glycan-mediated processes in various biological systems, paving the way for the development of novel research methodologies and the elucidation of complex molecular mechanisms underlying glycan function. This compound serves as a valuable asset in the arsenal of glycobiologists, enabling the exploration of glycan diversity and function in health and disease contexts.