
An overview of recent progress made toward nonpeptidic β-strand scaffolds is given. Reports between 1990-2003 are considered as well as few examples from broader reviews on peptide secondary structure. Focus is on inhibitors reported in crystallographic structures of protease-ligand complexes. Scaffolds are classified principally based on their heterocyclic subunits, although they may be perceived as amino acid surrogates elsewhere. An encyclopedia-style organization is adopted, according to compound class, to facilitate finding compounds, to identify structural similarities and differences, and particularly to compare different chemical types of β-stran mimetics.
Structure-based Design, Porcine Pancreatic Elastase, 780103 Chemical sciences, Multidisciplinary, Ring Constrained Peptidomimetics, Proteins, DNA, Matrix-metalloproteinase Inhibitors, Ligands, Human-leukocyte Elastase, Chemistry, C1, Chemical sciences, Peptide Hybrid Ligand, Biomimetic Materials, Drug Design, Ray Crystal-structure, Hiv-protease Inhibitors, Human Neutrophil Elastase, Humans, Angiotensin-converting Enzyme, 250301 Organic Chemical Synthesis
Structure-based Design, Porcine Pancreatic Elastase, 780103 Chemical sciences, Multidisciplinary, Ring Constrained Peptidomimetics, Proteins, DNA, Matrix-metalloproteinase Inhibitors, Ligands, Human-leukocyte Elastase, Chemistry, C1, Chemical sciences, Peptide Hybrid Ligand, Biomimetic Materials, Drug Design, Ray Crystal-structure, Hiv-protease Inhibitors, Human Neutrophil Elastase, Humans, Angiotensin-converting Enzyme, 250301 Organic Chemical Synthesis
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