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 |
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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. |
doi_str_mv | 10.1016/B978-0-12-381274-2.00017-0 |
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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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