Synthesis and biological evaluation of vancomycin dimers with potent activity against vancomycin-resistant bacteria: target-accelerated combinatorial synthesis.
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In situ assembly of enzyme inhibitors using extended tetheringSolid- and solution-phase synthesis of vancomycin and vancomycin analogues with activity against vancomycin-resistant bacteria.Solid phase synthesis of complex natural products and libraries thereof.Dynamic covalent chemistry on self-templating peptides: formation of a disulfide-linked beta-hairpin mimicBcl-XL-templated assembly of its own protein-protein interaction modulator from fragments decorated with thio acids and sulfonyl azides.Recent development of two chitinase inhibitors, Argifin and Argadin, produced by soil microorganisms.Polymerizable vancomycin derivatives for bactericidal biomaterial surface modification: structure-function evaluationDynamic combinatorial/covalent chemistry: a tool to read, generate and modulate the bioactivity of compounds and compound mixtures.Structural variations of the cell wall precursor lipid II and their influence on binding and activity of the lipoglycopeptide antibiotic oritavancin.Vancomycin: ligand recognition, dimerization and super-complex formation.Peptidoglycan architecture of Gram-positive bacteria by solid-state NMR.From nature to the laboratory and into the clinicThe essence of total synthesisConstructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.A stepwise dechlorination/cross-coupling strategy to diversify the vancomycin 'in-chloride'.Vancomycin forms ligand-mediated supramolecular complexes.Recent advances in the chemistry and biology of naturally occurring antibiotics.Probing secondary interactions in biomolecular recognition by dynamic combinatorial chemistry.Targeting a cell wall biosynthesis hot spot.A brief history of antibiotics and select advances in their synthesis.Reengineering Antibiotics to Combat Bacterial Resistance: Click Chemistry [1,2,3]-Triazole Vancomycin Dimers with Potent Activity against MRSA and VRE.Anti-cooperative ligand binding and dimerisation in the glycopeptide antibiotic dalbavancin.Supramolecular Antibiotic Switches: A Potential Strategy for Combating Drug Resistance.Binaphthyl-based dicationic peptoids with therapeutic potential.In situ click chemistry: enzyme-generated inhibitors of carbonic anhydrase II.Developments in Glycopeptide Antibiotics.
P2860
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P2860
Synthesis and biological evaluation of vancomycin dimers with potent activity against vancomycin-resistant bacteria: target-accelerated combinatorial synthesis.
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
name
Synthesis and biological evalu ...... rated combinatorial synthesis.
@ast
Synthesis and biological evalu ...... rated combinatorial synthesis.
@en
type
label
Synthesis and biological evalu ...... rated combinatorial synthesis.
@ast
Synthesis and biological evalu ...... rated combinatorial synthesis.
@en
prefLabel
Synthesis and biological evalu ...... rated combinatorial synthesis.
@ast
Synthesis and biological evalu ...... rated combinatorial synthesis.
@en
P2093
P2860
P1476
Synthesis and biological evalu ...... erated combinatorial synthesis
@en
P2093
H Labischinski
K C Nicolaou
R Endermann
P2860
P304
P356
10.1002/1521-3765(20010903)7:17<3824::AID-CHEM3824>3.0.CO;2-1
P407
P577
2001-09-01T00:00:00Z