Effective Progression of Nuclear Magnetic Resonance-Detected Fragment Hits

Fragment-based drug discovery (FBDD) has become increasingly popular over the last decade as an alternate lead generation tool to HTS approaches. Several compounds have now progressed into the clinic which originated from a fragment-based approach, demonstrating the utility of this emerging field. W...

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Veröffentlicht in:Methods in Enzymology 2011, Vol.493, p.447-468
Hauptverfasser: Eaton, Hugh L., Wyss, Daniel F.
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description Fragment-based drug discovery (FBDD) has become increasingly popular over the last decade as an alternate lead generation tool to HTS approaches. Several compounds have now progressed into the clinic which originated from a fragment-based approach, demonstrating the utility of this emerging field. While fragment hit identification has become much more routine and may involve different screening approaches, the efficient progression of fragment hits into quality lead series may still present a major bottleneck for the broadly successful application of FBDD. In our laboratory, we have extensive experience in fragment-based NMR screening (SbN) and the subsequent iterative progression of fragment hits using structure-assisted chemistry. To maximize impact, we have applied this approach strategically to early- and high-priority targets, and those struggling for leads. Its application has yielded a clinical candidate for BACE1 and lead series in about one third of the SbN/FBDD projects. In this chapter, we will give an overview of our strategy and focus our discussion on NMR-based FBDD approaches.
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subjects Amyloid Precursor Protein Secretases - antagonists & inhibitors
Amyloid Precursor Protein Secretases - metabolism
Aspartic Acid Endopeptidases - antagonists & inhibitors
Aspartic Acid Endopeptidases - metabolism
Biophysical Phenomena
Catalytic Domain - drug effects
Drug Design
Drug Discovery
Drug Evaluation, Preclinical - methods
Humans
Hydantoins - metabolism
Ligands
Models, Molecular
Nuclear Magnetic Resonance, Biomolecular - methods
Protease Inhibitors - chemical synthesis
Protease Inhibitors - therapeutic use
Protein Binding
Small Molecule Libraries
Structure-Activity Relationship
Thermodynamics
Thiourea - analogs & derivatives
title Effective Progression of Nuclear Magnetic Resonance-Detected Fragment Hits
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