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Toward a Class-Independent Quantitative Structure−Activity Relationship Model for Uncouplers of Oxidative Phosphorylation
331
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Fluorescence Spectroscopic Profiling of Compound Libraries
376
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Flaviviral Protease Inhibitors Identified by Fragment-Based Library Docking into a Structure Generated by Molecular Dynamics
361
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Characterization of Chemical Libraries for Luciferase Inhibitory Activity
349
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Fragment-Based Design of Small Molecule X-Linked Inhibitor of Apoptosis Protein Inhibitors
372
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Decoys for Docking
355
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A High-Throughput Screen for Aggregation-Based Inhibition in a Large Compound Library
271
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De Novo Discovery of Serotonin N-Acetyltransferase Inhibitors
239
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Small Molecules Block the Polymerization of Z α1-Antitrypsin and Increase the Clearance of Intracellular Aggregates
191
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Assessing the Scaffold Diversity of Screening Libraries
137
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