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      Open-source platform to benchmark fingerprints for ligand-based virtual screening

      research-article
      1 , 1 ,
      Journal of Cheminformatics
      BioMed Central
      Virtual screening, Benchmark, Similarity, Fingerprints

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          Abstract

          Similarity-search methods using molecular fingerprints are an important tool for ligand-based virtual screening. A huge variety of fingerprints exist and their performance, usually assessed in retrospective benchmarking studies using data sets with known actives and known or assumed inactives, depends largely on the validation data sets used and the similarity measure used. Comparing new methods to existing ones in any systematic way is rather difficult due to the lack of standard data sets and evaluation procedures. Here, we present a standard platform for the benchmarking of 2D fingerprints. The open-source platform contains all source code, structural data for the actives and inactives used (drawn from three publicly available collections of data sets), and lists of randomly selected query molecules to be used for statistically valid comparisons of methods. This allows the exact reproduction and comparison of results for future studies. The results for 12 standard fingerprints together with two simple baseline fingerprints assessed by seven evaluation methods are shown together with the correlations between methods. High correlations were found between the 12 fingerprints and a careful statistical analysis showed that only the two baseline fingerprints were different from the others in a statistically significant way. High correlations were also found between six of the seven evaluation methods, indicating that despite their seeming differences, many of these methods are similar to each other.

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          The properties of known drugs. 1. Molecular frameworks.

          In order to better understand the common features present in drug molecules, we use shape description methods to analyze a database of commercially available drugs and prepare a list of common drug shapes. A useful way of organizing this structural data is to group the atoms of each drug molecule into ring, linker, framework, and side chain atoms. On the basis of the two-dimensional molecular structures (without regard to atom type, hybridization, and bond order), there are 1179 different frameworks among the 5120 compounds analyzed. However, the shapes of half of the drugs in the database are described by the 32 most frequently occurring frameworks. This suggests that the diversity of shapes in the set of known drugs is extremely low. In our second method of analysis, in which atom type, hybridization, and bond order are considered, more diversity is seen; there are 2506 different frameworks among the 5120 compounds in the database, and the most frequently occurring 42 frameworks account for only one-fourth of the drugs. We discuss the possible interpretations of these findings and the way they may be used to guide future drug discovery research.
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            Atom pairs as molecular features in structure-activity studies: definition and applications

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              Multiple Hypothesis Testing in Microarray Experiments

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                Author and article information

                Journal
                J Cheminform
                J Cheminform
                Journal of Cheminformatics
                BioMed Central
                1758-2946
                2013
                30 May 2013
                : 5
                : 26
                Affiliations
                [1 ]Novartis Institutes for BioMedical Research, Basel, Switzerland
                Article
                1758-2946-5-26
                10.1186/1758-2946-5-26
                3686626
                23721588
                37c4a2ce-3385-4a4d-b6e6-e496b8340bd5
                Copyright ©2013 Riniker and Landrum; licensee Chemistry Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 3 April 2013
                : 20 May 2013
                Categories
                Research Article

                Chemoinformatics
                virtual screening,benchmark,similarity,fingerprints
                Chemoinformatics
                virtual screening, benchmark, similarity, fingerprints

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