1019642-47-7

Basic information

• Product Name: 2-azidoethyl α-5-acetamido-9-(biphenylcarbonylamino)-3,5,9-trideoxy-D-glycero-2-nonulosonic acid-pyranosyl-(2->3)-β-D-galactopyranosyl-(1->3)-2-acetamido-2-deoxy-glucopyranoside
• Synonyms: 2-azidoethyl α-5-acetamido-9-(biphenylcarbonylamino)-3,5,9-trideoxy-D-glycero-2-nonulosonic acid-pyranosyl-(2->3)-β-D-galactopyranosyl-(1->3)-2-acetamido-2-deoxy-glucopyranoside
• CAS NO: 1019642-47-7
• Molecular Weight: 922.898
• Mol File: 1019642-47-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-azidoethyl α-5-acetamido-9-(biphenylcarbonylamino)-3,5,9-trideoxy-D-glycero-2-nonulosonic acid-pyranosyl-(2->3)-β-D-galactopyranosyl-(1->3)-2-acetamido-2-deoxy-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2-azidoethyl α-5-acetamido-9-(biphenylcarbonylamino)-3,5,9-trideoxy-D-glycero-2-nonulosonic acid-pyranosyl-(2->3)-β-D-galactopyranosyl-(1->3)-2-acetamido-2-deoxy-glucopyranoside(1019642-47-7)
• EPA Substance Registry System: 2-azidoethyl α-5-acetamido-9-(biphenylcarbonylamino)-3,5,9-trideoxy-D-glycero-2-nonulosonic acid-pyranosyl-(2->3)-β-D-galactopyranosyl-(1->3)-2-acetamido-2-deoxy-glucopyranoside(1019642-47-7)

Safety Data

• Hazardous Substances Data: 1019642-47-7(Hazardous Substances Data)

Upstream product

• 936547-18-1 C₂₄H₂₈N₂O₉ 
• 952585-00-1 uridine-5'-diphosphoglucose 
• 142072-12-6 2'-azidoethyl 2-acetamido-2-deoxy-β-D-glucopyranoside 
• 338971-38-3 2-azidoethyl (β-D-galactopyranosyl)-(1->4)-O-2-acetamido-2-deoxy-β-D-glucopyranoside 

Downstream Products

• 936547-19-2 2-aminoethyl 5-acetamido-9-(4-biphenylcarbonylamino)-3,5,9-trideoxy-α-D-glycero-D-galacto-2-nonulopyranosylonate-(2-6)-O-β-D-galactopyranosyl-(1-4)-O-2-acetamido-2-deoxy-β-D-glucopyranoside 

Relevant articles and documents

On-virus construction of polyvalent glycan ligands for cell-surface receptors

Glycans arrayed on the exterior of virus particles were used as substrates for glycosyltransferase reactions to build di- and trisaccharides from the virus surface. The resulting particles exhibited tight and specific associations with cognate receptors on beads and cells, in one example defeating in cis cell-surface interactions in a manner characteristic of polyvalent binding. Combined with the ability of viruses to provide structurally well-defined attachment points, the methodology provides a convenient and powerful way to prepare complex carbohydrate ligands for clustered receptors. Copyright