Design and synthesis of carbohydrate-based inhibitors of protein-carbohydrate interactions.
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[1] K. H. Kalk,et al. Structure of the 70-kDa soluble lytic transglycosylase complexed with bulgecin A. Implications for the enzymatic mechanism. , 1995, Biochemistry.
[2] G. Primofiore,et al. Synthesis of pyrrolo[3,4-c]pyridine derivatives possessing an acid group and their in vitro and in vivo evaluation as aldose reductase inhibitors , 1996 .
[3] E. Freire,et al. Thermodynamics of intersubunit interactions in cholera toxin upon binding to the oligosaccharide portion of its cell surface receptor, ganglioside GM1. , 1989, Biochemistry.
[4] E Garman,et al. Crystal structure of Vibrio cholerae neuraminidase reveals dual lectin-like domains in addition to the catalytic domain. , 1994, Structure.
[5] K. Moore,et al. Structures of human and porcine aldehyde reductase: an enzyme implicated in diabetic complications. , 1994, Acta crystallographica. Section D, Biological crystallography.
[6] S. Crennell,et al. Crystal structure of a bacterial sialidase (from Salmonella typhimurium LT2) shows the same fold as an influenza virus neuraminidase. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[7] T. Sixma,et al. Lactose binding to heat-labile enterotoxin revealed by X-ray crystallography , 1992, Nature.
[8] S. Cusack,et al. Structure of the influenza virus haemagglutinin complexed with its receptor, sialic acid , 1988, Nature.
[9] G. Whitesides,et al. Polyacrylamides Bearing Pendant α-Sialoside Groups Strongly Inhibit Agglutination of Erythrocytes by Influenza Virus: The Strong Inhibition Reflects Enhanced Binding through Cooperative Polyvalent Interactions , 1996 .
[11] Chi‐Huey Wong,et al. Ligand Recognition by E-Selectin: Synthesis, Inhibitory Activity and Conformational Analysis of Bivalent Sialyl Lewis x Analogs , 1995 .
[12] G M Whitesides,et al. Hemagglutinins from two influenza virus variants bind to sialic acid derivatives with millimolar dissociation constants: a 500-MHz proton nuclear magnetic resonance study. , 1989, Biochemistry.
[13] G. Jacob,et al. Glycosylation inhibitors in biology and medicine. , 1995, Current opinion in structural biology.
[14] G. Thoma,et al. Synthesis of a Sialyl Lewis x Mimic with Fixed Carboxylic Acid Group: Chemical Approach toward the Elucidation of the Bioactive Conformation of Sialyl Lewis x. , 1996, The Journal of organic chemistry.
[15] G. Petsko,et al. An anion binding site in human aldose reductase: mechanistic implications for the binding of citrate, cacodylate, and glucose 6-phosphate. , 1994, Biochemistry.
[16] N. Isaacs,et al. The catalytic domain of a bacterial lytic transglycosylase defines a novel class of lysozymes , 1995, Proteins.
[17] V. Villeret,et al. Crystal structure of spinach chloroplast fructose-1,6-bisphosphatase at 2.8 A resolution. , 1995, Biochemistry.
[18] T. G. Hill,et al. Carbohydrate materials bearing neuraminidase-resistant C-glycosides of sialic acid strongly inhibit the in vitro infectivity of influenza virus. , 1992, Journal of medicinal chemistry.
[19] P. Oates,et al. Aldose reductase inhibitors: recent developments. , 1993, Progress in drug research. Fortschritte der Arzneimittelforschung. Progres des recherches pharmaceutiques.
[20] F. G. Prendergast,et al. Mechanism of aldose reductase inhibition: binding of NADP+/NADPH and alrestatin-like inhibitors. , 1994, Biochemistry.
[21] M. S. Biggers,et al. General Preparation of 7-Substituted 4-Chromanones: Synthesis of a Potent Aldose Reductase Inhibitor , 1994 .
[22] G M Whitesides,et al. Effective inhibitors of hemagglutination by influenza virus synthesized from polymers having active ester groups. Insight into mechanism of inhibition. , 1995, Journal of medicinal chemistry.
[23] G. Air,et al. Structure-based inhibitors of influenza virus sialidase. A benzoic acid lead with novel interaction. , 1995, Journal of medicinal chemistry.
[24] Thilo Stehle,et al. Structure of murine polyomavirus complexed with an oligosaccharide receptor fragment , 1994, Nature.
[25] J. Turunen,et al. Synthesis of a divalent sialyl Lewis x O-glycan, a potent inhibitor of lymphocyte-endothelium adhesion. Evidence that multivalency enhances the saccharide binding to L-selectin. , 1995, European journal of biochemistry.
[26] Kuo-Sen Huang,et al. Insight into E-selectin/ligand interaction from the crystal structure and mutagenesis of the lec/EGF domains , 1994, Nature.
[27] L. Lasky. Selectin-carbohydrate interactions and the initiation of the inflammatory response. , 1995, Annual review of biochemistry.
[28] C. Bertozzi,et al. The selectins and their ligands. , 1994, Current opinion in cell biology.
[29] E. Garman,et al. Purification, crystallization and preliminary crystallographic study of neuraminidase from Vibrio cholerae and Salmonella typhimurium LT2. , 1992, Journal of molecular biology.
[30] Roger S. Holmes,et al. Enzymology and Molecular Biology of Carbonyl Metabolism 5 , 1995, Advances in Experimental Medicine and Biology.
[31] J. Martial,et al. Crystal structure of cholera toxin B‐pentamer bound to receptor GM1 pentasaccharide , 1994, Protein science : a publication of the Protein Society.
[32] F. Hayden,et al. Safety and efficacy of the neuraminidase inhibitor GG167 in experimental human influenza. , 1996, JAMA.
[33] S. Crennell,et al. The three domains of a bacterial sialidase: a beta-propeller, an immunoglobulin module and a galactose-binding jelly-roll. , 1995, Structure.
[34] C. Bertozzi,et al. Sulfated disaccharide inhibitors of L-selectin: deriving structural leads from a physiological selectin ligand. , 1995, Biochemistry.
[35] G. Petsko,et al. Tyrosine-48 is the proton donor and histidine-110 directs substrate stereochemical selectivity in the reduction reaction of human aldose reductase: enzyme kinetics and crystal structure of the Y48H mutant enzyme. , 1994, Biochemistry.
[36] W G Laver,et al. A sialic acid-derived phosphonate analog inhibits different strains of influenza virus neuraminidase with different efficiencies. , 1995, Journal of molecular biology.
[37] M. Itzstein,et al. Aldose reductase as a target for drug design: molecular modeling calculations on the binding of acyclic sugar substrates to the enzyme. , 1995 .
[38] Chi‐Huey Wong,et al. Synthesis of Biologically Active Sialyl Lewis X Mimetics , 1995 .
[39] David D. Manning,et al. Selectin-Saccharide Interactions: Revealing Structure-Function Relationships with Chemical Synthesis , 1995 .
[40] F A Quiocho,et al. An unlikely sugar substrate site in the 1.65 A structure of the human aldose reductase holoenzyme implicated in diabetic complications. , 1992, Science.
[41] S. Casnocha,et al. Multivalent sialyl-LeX: potent inhibitors of E-selectin-mediated cell adhesion; reagent for staining activated endothelial cells. , 1994, Glycobiology.