1362022-48-7

Upstream product

• 34246-23-6 benzyl D-glucopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 1235999-59-3 benzyl 2-azido-2-deoxy-4,6-O-(phenylmethylene)-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 1235999-57-1 (2R,4aR,7R,8R,8aS)-6-(benzyloxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxine-7,8-diol 

Downstream Products

• 1362022-50-1 C₂₇H₂₉N₃O₅ 
• 1362022-52-3 C₂₇H₂₈FN₃O₄ 
• 1362022-54-5 C₂₉H₃₂FNO₅ 
• 1362022-57-8 C₂₈H₃₁N₃O₅ 
• 1362022-60-3 C₃₄H₃₅N₃O₇S 
• 1362022-87-4 C₂₇H₃₁NO₄ 
• 1362022-64-7 C₂₉H₃₃NO₅ 
• 1362022-68-1 C₂₇H₂₉NO₅ 
• 1362022-70-5 C₃₆H₃₇NO₇ 
• 1362022-72-7 C₃₆H₃₉NO₇ 
• 1362022-74-9 C₃₆H₃₈FNO₆ 
• 1362022-80-7 C₃₂H₃₇NO₈ 
• 1362022-84-1 C₃₆H₃₉NO₆ 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of sialosides containing C7-modified sialic acids and their application in sialidase substrate specificity studies

Modifications at the glycerol side chain of sialic acid in sialosides modulate their recognition by sialic acid-binding proteins and sialidases. However, limited work has been focused on the synthesis and functional studies of sialosides with C7-modified

Probe sialidase substrate specificity using chemoenzymatically synthesized sialosides containing C9-modified sialic acid

A library of α2-3- and α2-6-linked sialyl galactosides containing C9-modified sialic acids was synthesized from C6-modified mannose derivatives using an efficient one-pot three-enzyme system. These sialosides were used in a high-throughput sialidase substrate specificity assay to elucidate the importance of C9-OH in sialidase recognition. The Royal Society of Chemistry 2012.