Multivalent glycoconjugate syntheses and applications using aromatic scaffolds.
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Multivalent Carbohydrate-Lectin Interactions: How Synthetic Chemistry Enables Insights into Nanometric RecognitionAromatic thioglycoside inhibitors against the virulence factor LecA from Pseudomonas aeruginosaA LecA ligand identified from a galactoside-conjugate array inhibits host cell invasion by Pseudomonas aeruginosaPhotochemical Isomerization and Topochemical Polymerization of the Programmed Asymmetric AmphiphilesSuFEx: a metal-free click ligation for multivalent biomolecules.Synthesis and solvodynamic diameter measurements of closely related mannodendrimers for the study of multivalent carbohydrate-protein interactions.Expeditive synthesis of trithiotriazine-cored glycoclusters and inhibition of Pseudomonas aeruginosa biofilm formationThe influence of the aromatic aglycon of galactoclusters on the binding of LecA: a case study with O-phenyl, S-phenyl, O-benzyl, S-benzyl, O-biphenyl and O-naphthyl aglycons.Understanding carbohydrate-protein interactions using homologous supramolecular chiral Ru(ii)-glyconanoclusters.Probing secondary interactions in biomolecular recognition by dynamic combinatorial chemistry.Fullerene sugar balls: a new class of biologically active fullerene derivatives.The multivalent effect in glycosidase inhibition: a new, rapidly emerging topic in glycoscience.Design and Synthesis of Galactosylated Bifurcated Ligands with Nanomolar Affinity for Lectin LecA from Pseudomonas aeruginosa.Toward the Rational Design of Galactosylated Glycoclusters That Target Pseudomonas aeruginosa Lectin A (LecA): Influence of Linker Arms That Lead to Low-Nanomolar Multivalent Ligands.Dendritic glycopolymers based on dendritic polyamine scaffolds: view on their synthetic approaches, characteristics and potential for biomedical applications.Galectin Binding to Neo-Glycoproteins: LacDiNAc Conjugated BSA as Ligand for Human Galectin-3.Glyconanosynthons as powerful scaffolds and building blocks for the rapid construction of multifaceted, dense and chiral dendrimers.Nanomolar cholera toxin inhibitors based on symmetrical pentavalent ganglioside GM1os-sym-corannulenes.Emerging trends in enzyme inhibition by multivalent nanoconstructs.Sulfated glycopeptide nanostructures for multipotent protein activation.PPI-G4 Glycodendrimers Upregulate TRAIL-Induced Apoptosis in Chronic Lymphocytic Leukemia Cells.Sugared biomaterial binding lectins: achievements and perspectives.Nanotechnology in Glycomics: Applications in Diagnostics, Therapy, Imaging, and Separation Processes.Iminosugar-Cyclopeptoid Conjugates Raise Multivalent Effect in Glycosidase Inhibition at Unprecedented High Levels.Exploring the Influence of Shapes and Heterogeneity of Glyco-Gold Nanoparticles on Bacterial Binding for Preventing Infections.Biologically Active Heteroglycoclusters Constructed on a Pillar[5]arene-Containing [2]Rotaxane Scaffold.Tumour-Targeted Drug Delivery with Mannose-Functionalized Nanoparticles Self-Assembled from Amphiphilic β-Cyclodextrins.Pentavalent pillar[5]arene-based glycoclusters and their multivalent binding to pathogenic bacterial lectins.Solution Behavior of Amphiphilic Glycodendrimers with a Rod-Like Core.Glyconanomaterials for Combating Bacterial Infections.Assessing the effect of different shapes of glyco-gold nanoparticles on bacterial adhesion and infections.Effects of dendritic core-shell glycoarchitectures on primary mesenchymal stem cells and osteoblasts obtained from different human donorsSynthesis of a New Series of Sialylated Homo- and Heterovalent Glycoclusters by using Orthogonal Ligations.Postsynthetic functionalization of glycodendrons at the focal point.Tetravalent glycocyclopeptide with nanomolar affinity to wheat germ agglutinin.Fullerene-sp2-iminosugar balls as multimodal ligands for lectins and glycosidases: a mechanistic hypothesis for the inhibitory multivalent effect.Controlled ROS production by corannulene: the vehicle makes a difference.The Impact of Heteromultivalency in Lectin Recognition and Glycosidase Inhibition: An Integrated Mechanistic Study.Perylenediimide-based glycoclusters as high affinity ligands of bacterial lectins: synthesis, binding studies and anti-adhesive properties.Fullerene hexa-adduct scaffolding for the construction of giant molecules.
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Multivalent glycoconjugate syntheses and applications using aromatic scaffolds.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
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name
Multivalent glycoconjugate syntheses and applications using aromatic scaffolds.
@en
type
label
Multivalent glycoconjugate syntheses and applications using aromatic scaffolds.
@en
prefLabel
Multivalent glycoconjugate syntheses and applications using aromatic scaffolds.
@en
P2860
P356
P1476
Multivalent glycoconjugate syntheses and applications using aromatic scaffolds.
@en
P2093
Yoann M Chabre
P2860
P304
P356
10.1039/C3CS35483K
P577
2013-02-12T00:00:00Z