Fluorescence spectroscopic profiling of compound libraries.
about
High-affinity inhibitors of human NAD-dependent 15-hydroxyprostaglandin dehydrogenase: mechanisms of inhibition and structure-activity relationshipsDevelopment and utility of an in vitro, fluorescence-based assay for the discovery of novel compounds against dengue 2 viral proteaseApplications of Replicating-Competent Reporter-Expressing Viruses in Diagnostic and Molecular VirologyCan Invalid Bioactives Undermine Natural Product-Based Drug Discovery?Physicochemical characterization of a thermostable alcohol dehydrogenase from Pyrobaculum aerophilumComplementarity Between a Docking and a High-Throughput Screen in Discovering New Cruzain InhibitorsQuantitative High-Throughput Screening Identifies 8-Hydroxyquinolines as Cell-Active Histone Demethylase InhibitorsRational methods for the selection of diverse screening compoundsIdentification and characterization of inhibitors of human apurinic/apyrimidinic endonuclease APE1Novel patient cell-based HTS assay for identification of small molecules for a lysosomal storage diseaseA dual read-out assay to evaluate the potency of compounds active against Mycobacterium tuberculosisPerspectives on validation of high-throughput assays supporting 21st century toxicity testingSelective small molecule inhibitor of the Mycobacterium tuberculosis fumarate hydratase reveals an allosteric regulatory siteModeling error in experimental assays using the bootstrap principle: understanding discrepancies between assays using different dispensing technologies.Docking Screens for Novel Ligands Conferring New Biology.Quantitative analyses of aggregation, autofluorescence, and reactivity artifacts in a screen for inhibitors of a thiol proteaseHigh-throughput identification of promiscuous inhibitors from screening libraries with the use of a thiol-containing fluorescent probeA Quantitative High-Throughput Screening Data Analysis Pipeline for Activity Profiling.A high throughput fluorescence polarization assay for inhibitors of the GoLoco motif/G-alpha interaction.A specific mechanism for nonspecific activation in reporter-gene assaysA robotic platform for quantitative high-throughput screeningIdentification of phosphotyrosine mimetic inhibitors of human tyrosyl-DNA phosphodiesterase I by a novel AlphaScreen high-throughput assayCharacterization and optimization of a red-shifted fluorescence polarization ADP detection assay.Advances in improving the quality and flexibility of compound management.A dual-fluorescence high-throughput cell line system for probing multidrug resistance.A quantitative high-throughput screen for modulators of IL-6 signaling: a model for interrogating biological networks using chemical librariesThe pilot phase of the NIH Chemical Genomics Center.The identification, characterization and optimization of small molecule probes of cysteine proteases: experiences of the Penn Center for Molecular Discovery with cathepsin B and cathepsin L.A strategy to discover inhibitors of Bacillus subtilis surfactin-type phosphopantetheinyl transferase.Apparent activity in high-throughput screening: origins of compound-dependent assay interferenceA high-throughput screening compatible assay for activators and inhibitors of methionine sulfoxide reductase AA homogeneous method for investigation of methylation-dependent protein-protein interactions in epigeneticsIdentifying actives from HTS data sets: practical approaches for the selection of an appropriate HTS data-processing method and quality control review.A fluorescent, reagentless biosensor for ADP based on tetramethylrhodamine-labeled ParM.A quantitative high-throughput screen identifies novel inhibitors of the interaction of thyroid receptor beta with a peptide of steroid receptor coactivator 2Chemical genomics profiling of environmental chemical modulation of human nuclear receptors.Exploratory analysis of kinetic solubility measurements of a small molecule libraryComposition and applications of focus libraries to phenotypic assaysIdentification and characterization of novel inhibitors of Mammalian aspartyl aminopeptidaseIlluminating insights into firefly luciferase and other bioluminescent reporters used in chemical biology
P2860
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P2860
Fluorescence spectroscopic profiling of compound libraries.
description
2008 nî lūn-bûn
@nan
2008 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մարտին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Fluorescence spectroscopic profiling of compound libraries.
@ast
Fluorescence spectroscopic profiling of compound libraries.
@en
Fluorescence spectroscopic profiling of compound libraries.
@nl
type
label
Fluorescence spectroscopic profiling of compound libraries.
@ast
Fluorescence spectroscopic profiling of compound libraries.
@en
Fluorescence spectroscopic profiling of compound libraries.
@nl
prefLabel
Fluorescence spectroscopic profiling of compound libraries.
@ast
Fluorescence spectroscopic profiling of compound libraries.
@en
Fluorescence spectroscopic profiling of compound libraries.
@nl
P2093
P50
P356
P1476
Fluorescence spectroscopic profiling of compound libraries.
@en
P2093
Craig J Thomas
Douglas S Auld
James Inglese
Jeremy Smith
Paul Shinn
Ruili Huang
Yuhong Wang
P304
P356
10.1021/JM701301M
P407
P577
2008-03-26T00:00:00Z