By careful selection and experimental design, fragments can provide very useful starting points for medicinal chemistry-driven programmes, leading to tailor-made, selective molecules with highly favourable physico-chemical and ADMET properties
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[1] A. Hopkins,et al. Navigating chemical space for biology and medicine , 2004, Nature.
[2] M. Congreve,et al. A 'rule of three' for fragment-based lead discovery? , 2003, Drug discovery today.
[3] Andrew R Leach,et al. Fragment screening: an introduction. , 2006, Molecular bioSystems.
[4] Glyn Williams,et al. Fragment-based screening using X-ray crystallography and NMR spectroscopy. , 2007, Current opinion in chemical biology.
[5] Walter Huber,et al. A new strategy for improved secondary screening and lead optimization using high‐resolution SPR characterization of compound–target interactions , 2005, Journal of molecular recognition : JMR.
[6] Edgar Jacoby,et al. Library design for fragment based screening. , 2005, Current topics in medicinal chemistry.
[7] P. Hajduk,et al. Privileged molecules for protein binding identified from NMR-based screening. , 2000, Journal of medicinal chemistry.
[8] Zartler Er,et al. Protein NMR-based screening in drug discovery. , 2006 .
[9] A. Hopkins,et al. Ligand efficiency: a useful metric for lead selection. , 2004, Drug discovery today.
[10] Sid Topiol,et al. Use of the X-ray structure of the Beta2-adrenergic receptor for drug discovery. , 2008, Bioorganic & medicinal chemistry letters.
[11] P. Hajduk,et al. A decade of fragment-based drug design: strategic advances and lessons learned , 2007, Nature Reviews Drug Discovery.
[12] Karl Edman,et al. Novel prostaglandin D synthase inhibitors generated by fragment-based drug design. , 2008, Journal of medicinal chemistry.
[13] T. Sixma,et al. Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors , 2001, Nature.
[14] C. Lindsley,et al. Discovery of positive allosteric modulators of metabotropic glutamate receptor subtype 5 (mGluR5). , 2005, Current topics in medicinal chemistry.
[15] Brian K. Shoichet,et al. Virtual screening of chemical libraries , 2004, Nature.
[16] B. Kobilka,et al. New G-protein-coupled receptor crystal structures: insights and limitations. , 2008, Trends in pharmacological sciences.
[17] Tudor I. Oprea,et al. Pursuing the leadlikeness concept in pharmaceutical research. , 2004, Current opinion in chemical biology.
[18] A. Hopkins,et al. The druggable genome , 2002, Nature Reviews Drug Discovery.