Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by submonomer solid-phase synthesis
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Structural features of peptoid-peptide hybrids in lipid-water interfacesRational optimization of a HIV-1 Tat inhibitor: rapid progress on combinatorial lead structuresAn inhibitor of the Tat/TAR RNA interaction that effectively suppresses HIV-1 replicationIn Vivo, In Vitro, and In Silico Characterization of Peptoids as Antimicrobial AgentsSystematic conformational investigations of peptoids and peptoid-peptide chimeras.Biomimetic peptoid oligomers as dual-action antifreeze agentsSynthesis of highly substituted 5-(trifluoromethyl)ketoimidazoles using a mixed-solid/solution phase motif.A combinatorial peptoid library for the identification of novel MSH and GRP/bombesin receptor ligands.Towards vast libraries of scaffold-diverse, conformationally constrained oligomers.Library design concepts and implementation strategies.Discovery of a small molecule Tat-trans-activation-responsive RNA antagonist that potently inhibits human immunodeficiency virus-1 replication.Iterative exponential growth of stereo- and sequence-controlled polymers.Synthesis and complexing properties of cyclic benzylopeptoids - a new family of extended macrocyclic peptoids.A combinatorial approach to the discovery of efficient cationic peptoid reagents for gene delivery.A high-throughput assay for assessing the cell permeability of combinatorial libraries.Optimized protocols for the isolation of specific protein-binding peptides or peptoids from combinatorial libraries displayed on beads.Characterizing the structure and dynamics of folded oligomers: Pulsed ESR studies of peptoid helices.Discovering ligands for a microRNA precursor with peptoid microarrays.Modulation of human estrogen receptor α activity by multivalent estradiol-peptidomimetic conjugates.Close mimicry of lung surfactant protein B by "clicked" dimers of helical, cationic peptoids.Precisely tuneable energy transfer system using peptoid helix-based molecular scaffold.Multicomponent synthesis of acylated short peptoids with antifungal activity against plant pathogens.Development of homomultimers and heteromultimers of lung cancer-specific peptoids.A biomimetic polyketide-inspired approach to small-molecule ligand discovery.Assembly and molecular order of two-dimensional peptoid nanosheets through the oil-water interfacePeptoid-Peptide hybrid ligands targeting the polo box domain of polo-like kinase 1.Chemical-biological exploration of the limits of the Ras de- and repalmitoylating machinery.Synthesis of libraries of peptidomimetic compounds containing a 2-oxopiperazine unit in the main chain.A readily applicable strategy to convert peptides to peptoid-based therapeutics.Decoding split and pool combinatorial libraries with electron-transfer dissociation tandem mass spectrometryProtein, cell and bacterial fouling resistance of polypeptoid-modified surfaces: effect of side-chain chemistry.Cell Penetrating Peptoids (CPPos): Synthesis of a Small Combinatorial Library by Using IRORI MiniKans.Synthesis of molecularly encoded oligomers using a chemoselective "AB + CD" iterative approach.Electron capture dissociation studies of the fragmentation patterns of doubly protonated and mixed protonated-sodiated peptoids.Simultaneous detection of 19 K-ras mutations by free-solution conjugate electrophoresis of ligase detection reaction products on glass microchips.Propargylamine-isothiocyanate reaction: efficient conjugation chemistry in aqueous media.The identification of high-affinity G protein-coupled receptor ligands from large combinatorial libraries using multicolor quantum dot-labeled cell-based screening.Solid-phase synthesis of peptoid-like oligomers containing diverse diketopiperazine unitsSequence Programmable Peptoid Polymers for Diverse Materials Applications.NMEGylation: a novel modification to enhance the bioavailability of therapeutic peptides.
P2860
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P2860
Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by submonomer solid-phase synthesis
description
im Dezember 1992 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 1992
@uk
name
Efficient method for the preparation of peptoids [oligo
@nl
Efficient method for the prepa ...... bmonomer solid-phase synthesis
@en
type
label
Efficient method for the preparation of peptoids [oligo
@nl
Efficient method for the prepa ...... bmonomer solid-phase synthesis
@en
prefLabel
Efficient method for the preparation of peptoids [oligo
@nl
Efficient method for the prepa ...... bmonomer solid-phase synthesis
@en
P2093
P356
P1476
Efficient method for the prepa ...... bmonomer solid-phase synthesis
@en
P2093
Janice M. Kerr
Ronald N. Zuckermann
Stephen B. H. Kent
Walter H. Moos
P304
10646-10647
P356
10.1021/JA00052A076
P407
P577
1992-12-01T00:00:00Z