Lead optimization studies on FimH antagonists: discovery of potent and orally bioavailable ortho-substituted biphenyl mannosides
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The arsenal of pathogens and antivirulence therapeutic strategies for disarming themPerspective: Adhesion Mediated Signal Transduction in Bacterial PathogensThe tyrosine gate of the bacterial lectin FimH: a conformational analysis by NMR spectroscopy and X-ray crystallographyThe Antiadhesive Strategy in Crohn's Disease: Orally Active Mannosides to Decolonize Pathogenic Escherichia coli from the GutInflammation-Induced Adhesin-Receptor Interaction Provides a Fitness Advantage to Uropathogenic E. coli during Chronic InfectionUrinary Tract Infection: Pathogenesis and Outlook.Mutation of Tyr137 of the universal Escherichia coli fimbrial adhesin FimH relaxes the tyrosine gate prior to mannose binding.Human Urine Decreases Function and Expression of Type 1 Pili in Uropathogenic Escherichia coli.Second generation of thiazolylmannosides, FimH antagonists for E. coli-induced Crohn's disease.Combinatorial small-molecule therapy prevents uropathogenic Escherichia coli catheter-associated urinary tract infections in mice.Antivirulence Isoquinolone Mannosides: Optimization of the Biaryl Aglycone for FimH Lectin Binding Affinity and Efficacy in the Treatment of Chronic UTI.Targeting the bacteria-host interface: strategies in anti-adhesion therapy.Sugar administration is an effective adjunctive therapy in the treatment of Pseudomonas aeruginosa pneumoniaFrom physiology to pharmacy: developments in the pathogenesis and treatment of recurrent urinary tract infectionsBinuclear copper(II) complexes discriminating epimeric glycosides and α- and β-glycosidic bonds in aqueous solution.New and alternative approaches to tackling antibiotic resistance.Use of tetravalent galabiose for inhibition of streptococcus suis serotype 2 infection in a mouse modelToward the Rational Design of Galactosylated Glycoclusters That Target Pseudomonas aeruginosa Lectin A (LecA): Influence of Linker Arms That Lead to Low-Nanomolar Multivalent Ligands.Effect of Aminophenyl and Aminothiahexyl α-D-Glycosides of the Manno-, Gluco-, and Galacto-Series on Type 1 Fimbriae-Mediated Adhesion of Escherichia coli.The potential of FimH as a novel therapeutic target for the treatment of Crohn's disease.Mannose-derived FimH antagonists: a promising anti-virulence therapeutic strategy for urinary tract infections and Crohn's disease.Anti-virulence Strategies to Target Bacterial Infections.Inhibition of type 1 fimbriae-mediated Escherichia coli adhesion and biofilm formation by trimeric cluster thiomannosides conjugated to diamond nanoparticles.Small Molecules That Sabotage Bacterial Virulence.Strategies for combating bacterial biofilms: A focus on anti-biofilm agents and their mechanisms of action.Rational design strategies for FimH antagonists: new drugs on the horizon for urinary tract infection and Crohn's disease.UroPathogenic Escherichia coli (UPEC) Infections: Virulence Factors, Bladder Responses, Antibiotic, and Non-antibiotic Antimicrobial Strategies.Sites for Dynamic Protein-Carbohydrate Interactions of O- and C-Linked Mannosides on the E. coli FimH Adhesin.Selective depletion of uropathogenic E. coli from the gut by a FimH antagonist.Antivirulence C-Mannosides as Antibiotic-Sparing, Oral Therapeutics for Urinary Tract InfectionsThe Conformational Variability of FimH: Which Conformation Represents the Therapeutic Target?Development of Heptylmannoside-Based Glycoconjugate Antiadhesive Compounds against Adherent-Invasive Escherichia coli Bacteria Associated with Crohn's Disease.Conformational Switch of the Bacterial Adhesin FimH in the Absence of the Regulatory Domain - Engineering a Minimalistic Allosteric System.Virulence-targeted Antibacterials: Concept, Promise, and Susceptibility to Resistance Mechanisms.Physiochemical Tuning of Potent Escherichia coli Anti-Adhesives by Microencapsulation and Methylene Homologation.Glycan-functionalized diamond nanoparticles as potent E. coli anti-adhesives.Synthesis of branched-phosphodiester and mannose-centered fucosylated glycoclusters and their binding studies with Burkholderia ambifaria lectin (BambL)
P2860
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P2860
Lead optimization studies on FimH antagonists: discovery of potent and orally bioavailable ortho-substituted biphenyl mannosides
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Lead optimization studies on F ...... ubstituted biphenyl mannosides
@ast
Lead optimization studies on F ...... ubstituted biphenyl mannosides
@en
type
label
Lead optimization studies on F ...... ubstituted biphenyl mannosides
@ast
Lead optimization studies on F ...... ubstituted biphenyl mannosides
@en
prefLabel
Lead optimization studies on F ...... ubstituted biphenyl mannosides
@ast
Lead optimization studies on F ...... ubstituted biphenyl mannosides
@en
P2093
P2860
P356
P1476
Lead optimization studies on F ...... ubstituted biphenyl mannosides
@en
P2093
Corinne K Cusumano
Erik Chorell
Jan M Crowley
Jeffrey P Henderson
Jerome S Pinkner
Scott Campbell
Scott J Hultgren
Zhenfu Han
P2860
P304
P356
10.1021/JM300165M
P407
P577
2012-04-13T00:00:00Z