Scaffold Diversity Analysis of Compound Data Sets Using an Entropy-Based Measure
暂无分享,去创建一个
José L. Medina-Franco | Andreas Bender | Thomas Scior | Karina Martinez-Mayorga | J. Medina-Franco | A. Bender | K. Martínez-Mayorga | T. Scior | J. Medina‐Franco
[1] G. Bemis,et al. The properties of known drugs. 1. Molecular frameworks. , 1996, Journal of medicinal chemistry.
[2] Alban Arrault,et al. Managing, profiling and analyzing a library of 2.6 million compounds gathered from 32 chemical providers , 2006, Molecular Diversity.
[3] Gisbert Schneider,et al. Properties and Architecture of Drugs and Natural Products Revisited , 2007 .
[4] Tudor I. Oprea,et al. Scaffold Topologies. 2. Analysis of Chemical Databases , 2008, J. Chem. Inf. Model..
[5] Andrew C. Good,et al. Measuring CAMD technique performance: A virtual screening case study in the design of validation experiments , 2004, J. Comput. Aided Mol. Des..
[6] Mark Johnson,et al. Algorithm for Naming Molecular Equivalence Classes Represented by Labeled Pseudographs , 2001, J. Chem. Inf. Comput. Sci..
[7] P. Jaccard,et al. Etude comparative de la distribution florale dans une portion des Alpes et des Jura , 1901 .
[8] Andreas Bender,et al. “Plate Cherry Picking”: A Novel Semi-Sequential Screening Paradigm for Cheaper, Faster, Information-Rich Compound Selection , 2007, Journal of biomolecular screening.
[9] Rajarshi Guha,et al. Chemoinformatic Analysis of Combinatorial Libraries, Drugs, Natural Products, and Molecular Libraries Small Molecule Repository , 2009, J. Chem. Inf. Model..
[10] Gerald M. Maggiora,et al. Hierarchical Strategy for Identifying Active Chemotype Classes in Compound Databases , 2006, Chemical biology & drug design.
[11] R. Glen,et al. Molecular similarity: a key technique in molecular informatics. , 2004, Organic & biomolecular chemistry.
[12] Gisbert Schneider,et al. Scaffold diversity of natural products: inspiration for combinatorial library design. , 2008, Natural product reports.
[13] Mark Johnson,et al. Using Molecular Equivalence Numbers To Visually Explore Structural Features that Distinguish Chemical Libraries , 2002, J. Chem. Inf. Comput. Sci..
[14] Andreas Bender,et al. Similarity Searching of Chemical Databases Using Atom Environment Descriptors (MOLPRINT 2D): Evaluation of Performance , 2004, J. Chem. Inf. Model..
[15] G. Schneider,et al. Scaffold‐Hopping Potential of Ligand‐Based Similarity Concepts , 2006, ChemMedChem.
[16] Nathan Brown,et al. On scaffolds and hopping in medicinal chemistry. , 2006, Mini reviews in medicinal chemistry.
[17] A. Schuffenhauer,et al. Charting biologically relevant chemical space: a structural classification of natural products (SCONP). , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[18] A. H. Lipkus,et al. Structural Diversity of Organic Chemistry. a Scaffold Analysis of the Cas Registry , 2022 .
[19] Stefan Wetzel,et al. The Scaffold Tree - Visualization of the Scaffold Universe by Hierarchical Scaffold Classification , 2007, J. Chem. Inf. Model..
[20] Andreas Bender,et al. Diversity-oriented synthesis; a spectrum of approaches and results. , 2008, Organic & biomolecular chemistry.
[21] Didier Rognan,et al. Assessing the Scaffold Diversity of Screening Libraries , 2006, J. Chem. Inf. Model..
[22] Jun Xu. A new approach to finding natural chemical structure classes. , 2002, Journal of medicinal chemistry.
[23] Wolfgang H. B. Sauer,et al. Size doesn't matter: Scaffold diversity shape diversity, and biological activity of combinatorial libraries , 2003 .
[24] J. Bajorath,et al. Distribution of Molecular Scaffolds and R-Groups Isolated from Large Compound Databases , 1999 .
[25] J. Mason,et al. New 4-point pharmacophore method for molecular similarity and diversity applications: overview of the method and applications, including a novel approach to the design of combinatorial libraries containing privileged substructures. , 1999, Journal of medicinal chemistry.
[26] Thomas Scior,et al. Large compound databases for structure-activity relationships studies in drug discovery. , 2007, Mini reviews in medicinal chemistry.
[27] B. E. Evans,et al. Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists. , 1988, Journal of Medicinal Chemistry.
[28] Schmid,et al. "Scaffold-Hopping" by Topological Pharmacophore Search: A Contribution to Virtual Screening. , 1999, Angewandte Chemie.
[29] J. Irwin,et al. Benchmarking sets for molecular docking. , 2006, Journal of medicinal chemistry.
[30] Andreas Bender,et al. How Similar Are Similarity Searching Methods? A Principal Component Analysis of Molecular Descriptor Space , 2009, J. Chem. Inf. Model..
[31] Gisbert Schneider,et al. Collection of bioactive reference compounds for focused library design , 2003 .
[32] James L. Melville,et al. Better than Random? The Chemotype Enrichment Problem , 2009, J. Chem. Inf. Model..