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Predicting bioactive conformations and binding modes of macrocycles., , и . J. Comput. Aided Mol. Des., 30 (10): 841-849 (2016)Binding mode similarity measures for ranking of docking poses: a case study on the adenosine A2A receptor., и . J. Comput. Aided Mol. Des., 30 (6): 447-456 (2016)A general approach for retrosynthetic molecular core analysis., , , и . J. Cheminformatics, 11 (1): 61:1-61:9 (2019)Maximum common substructure-based Tversky index: an asymmetric hybrid similarity measure., , и . J. Comput. Aided Mol. Des., 30 (7): 523-531 (2016)Simplified activity cliff network representations with high interpretability and immediate access to SAR information., и . J. Comput. Aided Mol. Des., 34 (9): 943-952 (2020)Erratum to: Design of chemical space networks using a Tanimoto similarity variant based upon maximum common substructures., , , и . J. Comput. Aided Mol. Des., 29 (11): 1071-1072 (2015)From Qualitative to Quantitative Analysis of Activity and Property Landscapes., , , , и . J. Chem. Inf. Model., 60 (12): 5873-5880 (2020)Extraction of Discontinuous Structure-Activity Relationships from Compound Data Sets through Particle Swarm Optimization., , и . Journal of Chemical Information and Modeling, 51 (7): 1545-1551 (2011)Variability of Molecular Descriptors in Compound Databases Revealed by Shannon Entropy Calculations., , и . Journal of Chemical Information and Computer Sciences, 40 (3): 796-800 (2000)Assessing the Confidence Level of Public Domain Compound Activity Data and the Impact of Alternative Potency Measurements on SAR Analysis., и . Journal of Chemical Information and Modeling, 51 (12): 3131-3137 (2011)