Synthesis of dodecavalent fullerene-based glycoclusters and evaluation of their binding properties towards a bacterial lectin.
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Antibacterial Applications of NanodiamondsA Glycopeptide Dendrimer Inhibitor of the Galactose-Specific Lectin LecA and of Pseudomonas aeruginosa BiofilmsAromatic thioglycoside inhibitors against the virulence factor LecA from Pseudomonas aeruginosaA LecA ligand identified from a galactoside-conjugate array inhibits host cell invasion by Pseudomonas aeruginosaFucofullerenes as tight ligands of RSL and LecB, two bacterial lectins.Expeditive synthesis of trithiotriazine-cored glycoclusters and inhibition of Pseudomonas aeruginosa biofilm formationRational design and synthesis of optimized glycoclusters for multivalent lectin-carbohydrate interactions: influence of the linker arm.Analysis of carbohydrates and glycoconjugates by matrix-assisted laser desorption/ionization mass spectrometry: An update for 2011-2012.Exhaustive glycosylation, PEGylation, and glutathionylation of a [G4]-ene(48) dendrimer via photoinduced thiol-ene couplingMultivalent glycoconjugates as anti-pathogenic agentsGlyconanoparticles as multifunctional and multimodal carbohydrate systems.Glyconanotechnology.Multivalent glycoconjugate syntheses and applications using aromatic scaffolds.Bridging lectin binding sites by multivalent carbohydrates.Fullerene sugar balls: a new class of biologically active fullerene derivatives.Synthesis of highly functionalized C60 fullerene derivatives and their applications in material and life sciences.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.Synthesis of multivalent carbohydrate-centered glycoclusters as nanomolar ligands of the bacterial lectin LecA from Pseudomonas aeruginosa.CuAAC synthesis of resorcin[4]arene-based glycoclusters as multivalent ligands of lectins.Pseudomonas Aeruginosa Lectins As Targets for Novel Antibacterials.Biological and related applications of pillar[n]arenes.Biologically Active Heteroglycoclusters Constructed on a Pillar[5]arene-Containing [2]Rotaxane Scaffold.Pentavalent pillar[5]arene-based glycoclusters and their multivalent binding to pathogenic bacterial lectins.Functionalization of a Rigid Divalent Ligand for LecA, a Bacterial Adhesion Lectin.A versatile approach towards multivalent saccharide displays on magnetic nanoparticles and phospholipid vesicles.The inhibition of liposaccharide heptosyltransferase WaaC with multivalent glycosylated fullerenes: a new mode of glycosyltransferase inhibition.Fullerene-sp2-iminosugar balls as multimodal ligands for lectins and glycosidases: a mechanistic hypothesis for the inhibitory multivalent effect.Polycationic pillar[5]arene derivatives: interaction with DNA and biological applications.Glycosylated nanoscale surfaces: preparation and applications in medicine and molecular biology.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.Mechanistic Insight into Heptosyltransferase Inhibition by using Kdo Multivalent Glycoclusters.Pillar[5]arene-Based Glycoclusters: Synthesis and Multivalent Binding to Pathogenic Bacterial Lectins.Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry.Mannose-centered aromatic galactoclusters inhibit the biofilm formation of Pseudomonas aeruginosa.A highly versatile convergent/divergent "onion peel" synthetic strategy toward potent multivalent glycodendrimers.Conformational Preferences and the Phase Stability of Fullerene Hexa-adducts.Optimizing divalent inhibitors of Pseudomonas aeruginosa lectin LecA by using a rigid spacer.Convenient syntheses of fullerynes for 'clicking' into fullerene polymers.Multivalent Gold Glycoclusters: High Affinity Molecular Recognition by Bacterial Lectin PA-IL
P2860
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P2860
Synthesis of dodecavalent fullerene-based glycoclusters and evaluation of their binding properties towards a bacterial lectin.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Synthesis of dodecavalent full ...... es towards a bacterial lectin.
@en
Synthesis of dodecavalent full ...... es towards a bacterial lectin.
@nl
type
label
Synthesis of dodecavalent full ...... es towards a bacterial lectin.
@en
Synthesis of dodecavalent full ...... es towards a bacterial lectin.
@nl
prefLabel
Synthesis of dodecavalent full ...... es towards a bacterial lectin.
@en
Synthesis of dodecavalent full ...... es towards a bacterial lectin.
@nl
P2093
P2860
P50
P356
P1476
Synthesis of dodecavalent full ...... es towards a bacterial lectin.
@en
P2093
Jean-Pierre Praly
Julien Iehl
Samy Cecioni
Sébastien Vidal
Vincent Oerthel
P2860
P304
P356
10.1002/CHEM.201003258
P407
P577
2011-02-15T00:00:00Z