1363661-32-8

Upstream product

• 173029-44-2 phenyl (3,4-di-O-isopropylidene-β-D-galactopyranosyl)-(1->4)-1-thio-β-D-glucopyranoside 
• 152872-00-9 phenyl (2,6-di-O-acetyl-3,4-di-O-isopropylidene-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-thio-β-D-glucopyranoside 
• 27891-73-2 β-phenylsulfanyl lactoside 
• 1363661-30-6 phenyl (2,6-di-O-acetyl-4-O-(18)O-acetyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-thio-β-D-glucopyranoside 
• 1363661-27-1 phenyl (2,6-di-O-acetyl-4-O-(18)O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-thio-β-D-glucopyranoside 
• 1363661-24-8 phenyl (2,6-di-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-thio-β-D-glucopyranoside 

Downstream Products

• 1363661-34-0 phenyl ((3-(18)O)-β-D-(3-(18)O)galactopyranosyl)-(1->4)-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

Transition state analysis of Vibrio cholerae sialidase-catalyzed hydrolyses of natural substrate analogues

A series of isotopically labeled natural substrate analogues (phenyl 5-N-acetyl-α-d-neuraminyl-(2→3)-β-d-galactopyranosyl-(1→4) -1-thio-β-d-glucopyranoside; Neu5Acα2,3LacβSPh, and the corresponding 2→6 isomer) were prepared chemoenzymatically in order to