3D Matched Pairs: Integrating Ligand- and Structure-Based Knowledge for Ligand Design and Receptor Annotation
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[1] D. Covell,et al. A role for surface hydrophobicity in protein‐protein recognition , 1994, Protein science : a publication of the Protein Society.
[2] Stephen R. Johnson,et al. Trends in kinase selectivity: insights for target class-focused library screening. , 2011, Journal of medicinal chemistry.
[3] Andrew G. Leach,et al. Matched molecular pairs as a guide in the optimization of pharmaceutical properties; a study of aqueous solubility, plasma protein binding and oral exposure. , 2006, Journal of medicinal chemistry.
[4] T. Imai. Roles of water in protein structure and function studied by molecular liquid theory. , 2009, Frontiers in bioscience.
[5] Sarah Elizabeth Skerratt,et al. SAR mining and its application to the design of TRPA1 antagonists , 2012 .
[6] A. Mathiowetz,et al. Deep understanding of structure-solubility relationship for a diverse set of organic compounds using matched molecular pairs. , 2011, Bioorganic & medicinal chemistry.
[7] B. Honig,et al. Classical electrostatics in biology and chemistry. , 1995, Science.
[8] Francesca Milletti,et al. Targeted kinase selectivity from kinase profiling data. , 2012, ACS medicinal chemistry letters.
[9] Anne Mai Wassermann,et al. Advances in Computational Medicinal Chemistry: Matched Molecular Pair Analysis , 2012 .
[10] M. Verdonk,et al. SuperStar: comparison of CSD and PDB-based interaction fields as a basis for the prediction of protein-ligand interactions. , 2001, Journal of molecular biology.
[11] J. A. Grant,et al. A fast method of molecular shape comparison: A simple application of a Gaussian description of molecular shape , 1996, J. Comput. Chem..
[12] Mallur S. Madhusudhan,et al. DEPTH: a web server to compute depth and predict small-molecule binding cavities in proteins , 2011, Nucleic Acids Res..
[13] Y. Martin,et al. Do structurally similar molecules have similar biological activity? , 2002, Journal of medicinal chemistry.
[14] Anne Mai Wassermann,et al. A Data Mining Method To Facilitate SAR Transfer , 2011, J. Chem. Inf. Model..
[15] J. A. Grant,et al. A shape-based 3-D scaffold hopping method and its application to a bacterial protein-protein interaction. , 2005, Journal of medicinal chemistry.
[16] Barry C. Finzel,et al. Conserved Core Substructures in the Overlay of Protein-Ligand Complexes , 2011, J. Chem. Inf. Model..
[17] Paul A. Bartlett,et al. CAVEAT: A program to facilitate the design of organic molecules , 1994, J. Comput. Aided Mol. Des..
[18] Jürgen Bajorath,et al. Matched molecular pair analysis of small molecule microarray data identifies promiscuity cliffs and reveals molecular origins of extreme compound promiscuity. , 2012, Journal of medicinal chemistry.
[19] Daniel J. Warner,et al. Matched molecular pairs as a medicinal chemistry tool. , 2011, Journal of medicinal chemistry.
[20] Michael M. Hann,et al. RECAP-Retrosynthetic Combinatorial Analysis Procedure: A Powerful New Technique for Identifying Privileged Molecular Fragments with Useful Applications in Combinatorial Chemistry , 1998, J. Chem. Inf. Comput. Sci..
[21] Anne Mai Wassermann,et al. Systematic Assessment of Compound Series with SAR Transfer Potential , 2012, J. Chem. Inf. Model..
[22] A. Doweyko,et al. Synthesis and SAR of new pyrrolo[2,1-f][1,2,4]triazines as potent p38 alpha MAP kinase inhibitors. , 2008, Bioorganic & medicinal chemistry letters.
[23] Daniel J. Warner,et al. WizePairZ: A Novel Algorithm to Identify, Encode, and Exploit Matched Molecular Pairs with Unspecified Cores in Medicinal Chemistry , 2010, J. Chem. Inf. Model..
[24] Robert P. Sheridan,et al. The Most Common Chemical Replacements in Drug-Like Compounds , 2002, J. Chem. Inf. Comput. Sci..
[25] Emma Lees,et al. Structure-guided discovery of cyclin-dependent kinase inhibitors. , 2008, Biopolymers.
[26] G. Labesse,et al. LEA3D: a computer-aided ligand design for structure-based drug design. , 2005, Journal of medicinal chemistry.
[27] Lingle Wang,et al. Ligand binding to protein-binding pockets with wet and dry regions , 2011, Proceedings of the National Academy of Sciences.
[28] Stefan Güssregen,et al. Identification and Application of Antitarget Activity Hotspots to Guide Compound Optimization , 2011, Molecular informatics.
[29] Stefan Schmitt,et al. Do structurally similar ligands bind in a similar fashion? , 2006, Journal of medicinal chemistry.
[30] P. Willett. Searching techniques for databases of two- and three-dimensional chemical structures. , 2005, Journal of medicinal chemistry.
[31] Stephan C. Schürer,et al. Novel Kinase Inhibitors by Reshuffling Ligand Functionalities Across the Human Kinome , 2012, J. Chem. Inf. Model..
[32] John P. Overington,et al. ChEMBL: a large-scale bioactivity database for drug discovery , 2011, Nucleic Acids Res..
[33] W Patrick Walters,et al. CORES: an automated method for generating three-dimensional models of protein/ligand complexes. , 2004, Journal of medicinal chemistry.
[34] G. Bemis,et al. BREED: Generating novel inhibitors through hybridization of known ligands. Application to CDK2, p38, and HIV protease. , 2004, Journal of medicinal chemistry.
[35] Olivier Michielin,et al. SwissBioisostere: a database of molecular replacements for ligand design , 2012, Nucleic Acids Res..
[36] Visakan Kadirkamanathan,et al. Lead Optimization Using Matched Molecular Pairs: Inclusion of Contextual Information for Enhanced Prediction of hERG Inhibition, Solubility, and Lipophilicity , 2010, J. Chem. Inf. Model..
[37] Daniel Moser,et al. VAMMPIRE: a matched molecular pairs database for structure-based drug design and optimization. , 2013, Journal of medicinal chemistry.
[38] Daniel J Warner,et al. Prospective Prediction of Antitarget Activity by Matched Molecular Pairs Analysis , 2012, Molecular informatics.
[39] Ajay N. Jain,et al. Molecular Shape and Medicinal Chemistry: A Perspective , 2010, Journal of medicinal chemistry.