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1.
J Med Chem ; 50(6): 1124-32, 2007 Mar 22.
Article in English | MEDLINE | ID: mdl-17315857

ABSTRACT

Fragment-based lead discovery has been successfully applied to the aspartyl protease enzyme beta-secretase (BACE-1). Fragment hits that contained an aminopyridine motif binding to the two catalytic aspartic acid residues in the active site of the enzyme were the chemical starting points. Structure-based design approaches have led to identification of low micromolar lead compounds that retain these interactions and additionally occupy adjacent hydrophobic pockets of the active site. These leads form two subseries, for which compounds 4 (IC50 = 25 microM) and 6c (IC50 = 24 microM) are representative. In the latter series, further optimization has led to 8a (IC50 = 690 nM).


Subject(s)
Aminoquinolines/chemistry , Amyloid Precursor Protein Secretases/antagonists & inhibitors , Amyloid Precursor Protein Secretases/chemistry , Aspartic Acid Endopeptidases/antagonists & inhibitors , Aspartic Acid Endopeptidases/chemistry , Models, Molecular , Quantitative Structure-Activity Relationship , Aminoquinolines/chemical synthesis , Binding Sites , Crystallography, X-Ray , Humans , Indoles/chemical synthesis , Indoles/chemistry , Ligands , Protein Binding , Recombinant Proteins/antagonists & inhibitors , Recombinant Proteins/chemistry
2.
Drug Discov Today ; 10(14): 987-92, 2005 Jul 15.
Article in English | MEDLINE | ID: mdl-16023057

ABSTRACT

Fragment-based lead discovery (also referred to as needles, shapes, binding elements, seed templates or scaffolds) is a new lead discovery approach in which much lower molecular weight (120-250 Da) compounds are screened relative to HTS campaigns. Fragment-based hits are typically weak inhibitors (10 microM-mM), and therefore need to be screened at higher concentration using very sensitive biophysical detection techniques such as protein crystallography and NMR as the primary screening techniques, rather than bioassays. Compared with HTS hits, these fragments are simpler, less functionalized compounds with correspondingly lower affinity. However, fragment hits typically possess high 'ligand efficiency' (binding affinity per heavy atom) and so are highly suitable for optimization into clinical candidates with good drug-like properties.


Subject(s)
Drug Design , Technology, Pharmaceutical/methods , Magnetic Resonance Spectroscopy , Models, Molecular , Molecular Weight , Technology, Pharmaceutical/trends
3.
J Med Chem ; 48(2): 414-26, 2005 Jan 27.
Article in English | MEDLINE | ID: mdl-15658855

ABSTRACT

We describe the structure-guided optimization of the molecular fragments 2-amino-3-benzyloxypyridine 1 (IC(50) 1.3 mM) and 3-(2-(4-pyridyl)ethyl)indole 2 (IC(50) 35 microM) identified using X-ray crystallographic screening of p38alpha MAP kinase. Using two separate case studies, the article focuses on the key compounds synthesized, the structure-activity relationships and the binding mode observations made during this optimization process, resulting in two potent lead series that demonstrate significant increases in activity. We describe the process of compound elaboration either through the growing out from fragments into adjacent pockets or through the conjoining of overlapping fragments and demonstrate that we have exploited the mobile conserved activation loop, consisting in part of Asp168-Phe169-Gly170 (DFG), to generate significant improvements in potency and kinase selectivity.


Subject(s)
Aminopyridines/chemistry , Drug Design , Enzyme Inhibitors/chemistry , Indoles/chemistry , p38 Mitogen-Activated Protein Kinases/antagonists & inhibitors , Aminopyridines/chemical synthesis , Aminopyridines/pharmacology , Cell Line, Tumor , Crystallography, X-Ray , Databases, Factual , Humans , Indoles/chemical synthesis , Indoles/pharmacology , Ligands , Models, Molecular , Molecular Structure , Protein Binding , Quantitative Structure-Activity Relationship , p38 Mitogen-Activated Protein Kinases/chemistry
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