Generation of molecular diversity on N-acetyllactosamine via O-cyanomethyl ethers
- 1 August 1997
- journal article
- Published by Elsevier in Carbohydrate Research
- Vol. 303 (1) , 51-65
- https://doi.org/10.1016/s0008-6215(97)00142-0
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Key involvement of all three GlcNAc hydroxyl groups in the recognition of β-D-GlcpNAc-(1→2)-α-D-Manp-(1→6)-β-D-Glcp-OR by N-acetylglucosaminyltransferase-VBioorganic & Medicinal Chemistry, 1994
- Modulation of antibody affinity by synthetic modifications of the most exposed pyranose residue of a trisaccharide epitopeBioorganic & Medicinal Chemistry, 1994
- Synthetic substrate analogues for UDP-GlcNAc: Manα1-6R β(1-2)-N-acetylglucosaminyltransferase II. Substrate specificity and inhibitors for the enzymeGlycoconjugate Journal, 1994
- Rational design of potent sialidase-based inhibitors of influenza virus replicationNature, 1993
- Carbohydrate-protein interactions in antibodies and lectinsCurrent Opinion in Structural Biology, 1992
- Active site similarities of glucose dehydrogenase, glucose oxidase, and glucoamylase probed by deoxygenated substratesBiochemistry, 1992
- Recognition of a Cell-Surface Oligosaccharide of Pathogenic Salmonella by an Antibody Fab FragmentScience, 1991
- Mapping of subsites of monoclonal, anti-carbohydrate antibodies using deoxy and deoxyfluoro sugarsChemical Reviews, 1991
- Protein-carbohydrate interactions: basic molecular featuresPure and Applied Chemistry, 1989
- Rhône-Poulenc Lecture. The origin of the specificity in the recognition of oligosaccharides by proteinsChemical Society Reviews, 1989