130539-14-9

Upstream product

• 130609-18-6 N-benzyloxycarbonyl-1,5-dideoxy-1,5-imino-4,6-O-isopropylidene-D-glucitol 
• 100-39-0 benzyl bromide 
• 19130-96-2 1,5-dideoxy-1,5-imino-D-glucitol 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 161106-75-8 methyl 3-O-allyl-5-O-benzyl-N-benzyloxycarbonyl-2,6-dideoxy-2,6-imino-α-L-gulofuranoside 
• 372493-94-2 methyl 3-O-allyl-5-O-benzyl-N-benzyloxycarbonyl-2,6-dideoxy-2,6-imino-β-L-gulofuranoside 
• 161045-50-7 methyl 3-O-allyl-6-azido-5-O-benzyl-6-deoxy-β-L-idofuranoside 
• 161045-49-4 methyl 3-O-allyl-6-azido-5-O-benzyl-6-deoxy-α-L-idofuranoside 
• 372493-97-5 4-O-allyl-N-benzyloxycarbonyl-2,3-di-O-benzyl-6-O-tert-butyldiphenylsilyl-1,5-dideoxy-1,5-imino-D-gulcitol 
• 161045-46-1 3-O-allyl-6-O-benzoyl-1,2-O-isopropylidene-5-O-methanesulfonyl-α-D-glucofuranose 
• 161045-52-9 4-O-allyl-2-O-benzyl-N-benzyloxycarbonyl-1,5-dideoxy-1,5-imino-D-gulcitol 
• 161045-48-3 3-O-allyl-6-azido-5-O-benzyl-6-deoxy-1,2-O-isopropylidene-β-L-idofuranose 
• 161045-47-2 3-O-allyl-5,6-anhydro-1,2-O-isopropylidene-β-L-idofuranose 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 130539-15-0 2,3-di-O-benzyl-N,6-O-carbonyl-1,5-dideoxy-1,5-imino-D-glucitol 
• 130609-19-7 2,3-di-O-benzyl-N,6-O-carbonyl-1,5-dideoxy-1,5-imino-D-galactitol 
• 130539-17-2 4-O-benzoyl-2,3-di-O-benzyl-N,6-O-carbonyl-1,5-dideoxy-1,5-imino-D-galactitol 
• 130539-16-1 2,3-di-O-benzyl-N,6-O-carbonyl-1,5-dideoxy-1,5-imino-4-O-methanesulfonyl-D-glucitol 
• 130539-18-3 2,3-di-O-benzyl-1,5-dideoxy-1,5-imino-D-galactitol 
• 909100-33-0 2,3-di-O-benzyl-N-benzyloxycarbonyl-1,5-dideoxy-6-O-[β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl]-1,5-imino-D-glucitol 
• 909100-32-9 2,3-di-O-benzyl-N-benzyloxycarbonyl-1,5-dideoxy-6-O-β-D-glucopyranosyl-1,5-imino-D-glucitol 

Relevant academic research and scientific papers

1,3-Dideoxynojirimycin-3-yl glycosides of β-(1→3)- and β-(1→6)-linked gluco-oligosaccharides

Standard chemical methods involving the use of O-acetylated glycosyl trichloroacetimidates as glycosylating agents were used to prepare the five 1,3-dideoxynojirimycin-3-yl β-(1→3)-linked oligo-glucosides (1-5) and also the β-(1→6)-bonded glucobiose (gent

Design and synthesis of a heparanase inhibitor with pseudodisaccharide structure

Aza-analogue of the basic disaccharide unit of heparane sulfate was designed as a potent inhibitor against heparanase produced by solid tumors cell, and synthesized via a coupling reaction of phenyl 2-azide-1-thio-D-glucopyranoside derivatives with a partially protected 1-deoxynojirimycin derived from D-glucose. The azapseudodisaccharide inhibited tumor cell heparanase with IC50 value of 58-63 μM.