HAMS: High-Affinity Mass Spectrometry Screening. A High-Throughput Screening Method for Identifying the Tightest-Binding Lead Compounds for Target Proteins with No False Positive Identifications

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Rapid LC-MS Based High-Throughput Screening Method, Affording No False Positives or False Negatives, Identifies a New Inhibitor for Carbonic Anhydrase.Ligand identification of the adenosine A2A receptor in self-assembled nanodiscs by affinity mass spectrometry

P2860

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P2860

HAMS: High-Affinity Mass Spectrometry Screening. A High-Throughput Screening Method for Identifying the Tightest-Binding Lead Compounds for Target Proteins with No False Positive Identifications

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http://www.wikidata.org/entity/Q42677543

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

HAMS: High-Affinity Mass Spect ...... False Positive Identifications

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HAMS: High-Affinity Mass Spect ...... False Positive Identifications

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HAMS: High-Affinity Mass Spect ...... False Positive Identifications

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HAMS: High-Affinity Mass Spect ...... False Positive Identifications

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HAMS: High-Affinity Mass Spect ...... False Positive Identifications

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HAMS: High-Affinity Mass Spect ...... False Positive Identifications

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P1476

HAMS: High-Affinity Mass Spect ...... False Positive Identifications

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P2093

Eden P Go

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Kasun P Imaduwage

http://www.w3.org/2001/XMLSchema#string

Zhikai Zhu

http://www.w3.org/2001/XMLSchema#string

P2860

Expanding the number of 'druggable' targets: non-enzymes and protein-protein interactions

Applications of pulsed ultrafiltration-mass spectrometry.

Mass spectrometry and immobilized enzymes for the screening of inhibitor libraries.

A general technique to rank protein-ligand binding affinities and determine allosteric versus direct binding site competition in compound mixtures.

A chemoinformatics analysis of hit lists obtained from high-throughput affinity-selection screening.

Development and implementation of a 384-well homogeneous fluorescence intensity high-throughput screening assay to identify mitogen-activated protein kinase phosphatase-1 dual-specificity protein phosphatase inhibitors.

Recent developments in protein-ligand affinity mass spectrometry.

Application of high-throughput affinity-selection mass spectrometry for screening of chemical compound libraries in lead discovery.

Solution-based indirect affinity selection mass spectrometry--a general tool for high-throughput screening of pharmaceutical compound libraries.

P2888

s13361-016-1472-3

P304

1870-1877

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scholarly article

P356

10.1007/S13361-016-1472-3

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Heather Desaire

P577

2016-09-06T00:00:00Z

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1052689020

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27600575

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5501305

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HAMS: High-Affinity Mass Spectrometry Screening. A High-Throughput Screening Method for Identifying the Tightest-Binding Lead Compounds for Target Proteins with No False Positive Identifications

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P2860

P2860

HAMS: High-Affinity Mass Spectrometry Screening. A High-Throughput Screening Method for Identifying the Tightest-Binding Lead Compounds for Target Proteins with No False Positive Identifications

description

name

type

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932