658072-68-5

Upstream product

• 330846-47-4 α-NeuAc4NAcCOOBnXan 
• 658072-66-3 N-(9H-fluoren-9-yl)methoxycarbonyl-O-(2-acetamido-2-deoxy-3-O-[2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl]-α-D-galactopyranosyl)-L-serine tert-butyl ester 
• 912840-55-2 N-(9H-fluoren-9-yl-methoxycarbonyl)-O-(2-acetamido-2-deoxy-6-O-[benzyl-(5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranosyl)onate]-α-D-galactopyranosyl)-L-serine tert-butyl ester 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 

Relevant academic research and scientific papers

Saccharide-induced peptide conformation in glycopeptides of the recognition region of LI-cadherin

(Chemical Equation Presented) The type and the size of the saccharide side chain can affect the conformation of the peptide portion of glycopeptides. This was shown by conformational analysis in solution for a series of glycoundecapeptides with systematic

Synthesis of Peptide and Glycopeptide Partial Structures of the Homophilic Recognition Domain of Epithelial Cadherin

Peptide and glycopeptide sequences of the homophilic recognition site of epithelial cadherin (E-cadherin) were synthesized by solid-phase technique based on acid-sensitive Wang anchor according to Fmoc strategy. Fmoc serine building blocks with TN/s