Expansion of chemical space for collaborative lead generation and drug discovery: the European Lead Factory Perspective.
暂无分享,去创建一个
Adam Nelson | Tuomo Kalliokoski | Gerhard Müller | Fabrizio Giordanetto | Dimitrios Tzalis | Anna Karawajczyk | Jorg Benningshof | Daniel Hamza | Kees Pouwer | Remy Morgentin | Alexander Piechot | G. Müller | T. Kalliokoski | A. Nelson | R. Morgentin | F. Giordanetto | Kees Pouwer | A. Karawajczyk | D. Hamza | Dimitrios Tzalis | J. Benningshof | A. Piechot
[1] Tudor I. Oprea,et al. The Design of Leadlike Combinatorial Libraries. , 1999, Angewandte Chemie.
[2] Adam Nelson,et al. Exploitation of the Ugi–Joullié Reaction in the Synthesis of Libraries of Drug-Like Bicyclic Hydantoins , 2015 .
[3] Fabrizio Giordanetto,et al. Branching cascades provide access to two amino-oxazoline compound libraries. , 2015, Bioorganic & medicinal chemistry.
[4] Charles C. Persinger,et al. How to improve R&D productivity: the pharmaceutical industry's grand challenge , 2010, Nature Reviews Drug Discovery.
[5] Adam Nelson,et al. A systematic approach to diverse, lead-like scaffolds from α,α-disubstituted amino acids. , 2015, Chemical communications.
[6] Nathan Brown,et al. Plane of Best Fit: A Novel Method to Characterize the Three-Dimensionality of Molecules , 2012, J. Chem. Inf. Model..
[7] George Papadatos,et al. The ChEMBL bioactivity database: an update , 2013, Nucleic Acids Res..
[8] Jorge Sanchez-Quesada,et al. Design and synthesis of 1,1-disubstituted-1-silacycloalkane-based compound libraries. , 2015, Bioorganic & medicinal chemistry.
[9] C. Lipinski. Lead- and drug-like compounds: the rule-of-five revolution. , 2004, Drug discovery today. Technologies.
[10] Stuart L. Schreiber,et al. Quantifying structure and performance diversity for sets of small molecules comprising small-molecule screening collections , 2011, Proceedings of the National Academy of Sciences.
[11] F. Pammolli,et al. The productivity crisis in pharmaceutical R&D , 2011, Nature Reviews Drug Discovery.
[12] Adam Nelson,et al. Aminomethylhydroxylation of alkenes: Exploitation in the synthesis of scaffolds for small molecule libraries. , 2015, Bioorganic & medicinal chemistry.
[13] C. Wiesmann,et al. The discovery of first-in-class drugs: origins and evolution , 2014, Nature Reviews Drug Discovery.
[14] William Lewis,et al. Combining two-directional synthesis and tandem reactions. Part 21: Exploitation of a dimeric macrocycle for chain terminus differentiation and synthesis of an sp(3)-rich library. , 2015, Bioorganic & medicinal chemistry.
[15] Asher Mullard,et al. European Lead Factory opens for business , 2013, Nature Reviews Drug Discovery.
[16] C. Moody,et al. Seven-membered ring scaffolds for drug discovery: Access to functionalised azepanes and oxepanes through diazocarbonyl chemistry. , 2015, Bioorganic & medicinal chemistry.
[17] Herbert Waldmann,et al. Stereoselective synthesis of a natural product inspired tetrahydroindolo[2,3-a]-quinolizine compound library. , 2015, Bioorganic & medicinal chemistry.
[18] Alexander Dömling,et al. Efficient isocyanide-less isocyanide-based multicomponent reactions. , 2015, Organic letters.
[19] Mario van der Stelt,et al. Cyclopentitol as a scaffold for a natural product-like compound library for drug discovery. , 2015, Bioorganic & medicinal chemistry.
[20] Michael Williams,et al. Productivity Shortfalls in Drug Discovery: Contributions from the Preclinical Sciences? , 2011, Journal of Pharmacology and Experimental Therapeutics.
[21] S. Langston,et al. The Discovery of First-in-Class Inhibitors of the Nedd8-Activating Enzyme (NAE) and the Ubiquitin-Activating Enzyme (UAE) , 2017 .
[22] Wolfgang H. B. Sauer,et al. Molecular Shape Diversity of Combinatorial Libraries: A Prerequisite for Broad Bioactivity , 2003, J. Chem. Inf. Comput. Sci..
[23] Paul Morgan,et al. Can the flow of medicines be improved? Fundamental pharmacokinetic and pharmacological principles toward improving Phase II survival. , 2012, Drug discovery today.
[24] B. Munos,et al. Can Open‐Source Drug R&D Repower Pharmaceutical Innovation? , 2010, Clinical pharmacology and therapeutics.
[25] Alice McCarthy. The NIH Molecular Libraries Program: identifying chemical probes for new medicines. , 2010, Chemistry & biology.
[26] I. Khanna,et al. Drug discovery in pharmaceutical industry: productivity challenges and trends. , 2012, Drug discovery today.
[27] C. Humblet,et al. Escape from flatland: increasing saturation as an approach to improving clinical success. , 2009, Journal of medicinal chemistry.
[28] Thomas E Nielsen,et al. Synthesis of hexahydropyrrolo[2,1-a]isoquinoline compound libraries through a Pictet-Spengler cyclization/metal-catalyzed cross coupling/amidation sequence. , 2015, Bioorganic & medicinal chemistry.
[29] John G. Moffat,et al. Phenotypic screening in cancer drug discovery — past, present and future , 2014, Nature Reviews Drug Discovery.
[30] Markus Kaiser,et al. Synthesis of a hexahydropyrrolo indole (HPI) compound library. , 2015, Bioorganic & medicinal chemistry.
[31] A. H. Lipkus,et al. Structural Diversity of Organic Chemistry. a Scaffold Analysis of the Cas Registry , 2022 .
[32] Adam Nelson,et al. A unified lead-oriented synthesis of over fifty molecular scaffolds. , 2015, Organic & biomolecular chemistry.
[33] Thomas E Nielsen,et al. Synthesis of 1,4,5 trisubstituted γ-lactams via a 3-component cascade reaction. , 2015, Bioorganic & medicinal chemistry.
[34] Eberhardt Herdtweck,et al. Leuckart-Wallach Route Toward Isocyanides and Some Applications. , 2015, ACS combinatorial science.
[35] Mark J Wigglesworth,et al. Increasing the delivery of next generation therapeutics from high throughput screening libraries. , 2015, Current opinion in chemical biology.
[36] Fabrizio Giordanetto,et al. Potential strategies for increasing drug-discovery productivity. , 2014, Future medicinal chemistry.
[37] Adam Nelson,et al. Design, synthesis and decoration of molecular scaffolds for exploitation in the production of alkaloid-like libraries. , 2015, Bioorganic & medicinal chemistry.
[38] Andrew L Hopkins,et al. The Joint European Compound Library: boosting precompetitive research. , 2015, Drug discovery today.
[39] G. Bemis,et al. The properties of known drugs. 1. Molecular frameworks. , 1996, Journal of medicinal chemistry.
[40] Eberhardt Herdtweck,et al. MCR synthesis of a tetracyclic tetrazole scaffold. , 2015, Bioorganic & medicinal chemistry.
[41] F. Rutjes,et al. Synthesis and functionalization of bicyclic N,O-acetal scaffolds from furfural. , 2015, Bioorganic & Medicinal Chemistry.
[42] Asher Mullard. 2014 FDA drug approvals , 2015, Nature Reviews Drug Discovery.
[43] A. Harvey,et al. The re-emergence of natural products for drug discovery in the genomics era , 2015, Nature Reviews Drug Discovery.