Literature DB >> 27515428

Maximum common substructure-based Tversky index: an asymmetric hybrid similarity measure.

Ryo Kunimoto1, Martin Vogt1, Jürgen Bajorath2.   

Abstract

Current approaches for the assessment of molecular similarity can generally be divided into descriptor-based and substructure-based methods. The former require the application of similarity metrics that yield continuous similarity values, whereas the readout of the latter is binary (i.e. similar vs. not similar). However, it is also possible to combine descriptor-based and substructure-based methods to exploit advantages of individual methods in context and generate similarity measures for special applications. Herein we present a hybrid measure for asymmetric similarity calculations on the basis of maximum common core structures. This similarity function can be effectively applied to compare small reference compounds with larger test molecules, which is difficult using conventional metrics.

Keywords:  Hybrid measures; Maximum common substructure; Molecular similarity; Similarity metrics; Substructure methods; Tversky similarity

Mesh:

Year:  2016        PMID: 27515428     DOI: 10.1007/s10822-016-9935-y

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  16 in total

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Journal:  J Comput Aided Mol Des       Date:  2002-01       Impact factor: 3.686

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Authors:  Martin Vogt; Dagmar Stumpfe; Hanna Geppert; Jürgen Bajorath
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3.  Advanced fingerprint methods for similarity searching: balancing molecular complexity effects.

Authors:  Yuan Wang; Jürgen Bajorath
Journal:  Comb Chem High Throughput Screen       Date:  2010-03       Impact factor: 1.339

4.  Design of chemical space networks using a Tanimoto similarity variant based upon maximum common substructures.

Authors:  Bijun Zhang; Martin Vogt; Gerald M Maggiora; Jürgen Bajorath
Journal:  J Comput Aided Mol Des       Date:  2015-09-29       Impact factor: 3.686

5.  Balancing the influence of molecular complexity on fingerprint similarity searching.

Authors:  Yuan Wang; Jürgen Bajorath
Journal:  J Chem Inf Model       Date:  2007-12-15       Impact factor: 4.956

6.  Do not hesitate to use Tversky-and other hints for successful active analogue searches with feature count descriptors.

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Journal:  J Chem Inf Model       Date:  2013-06-13       Impact factor: 4.956

7.  Molecular similarity in medicinal chemistry.

Authors:  Gerald Maggiora; Martin Vogt; Dagmar Stumpfe; Jürgen Bajorath
Journal:  J Med Chem       Date:  2013-11-11       Impact factor: 7.446

8.  Computationally efficient algorithm to identify matched molecular pairs (MMPs) in large data sets.

Authors:  Jameed Hussain; Ceara Rea
Journal:  J Chem Inf Model       Date:  2010-03-22       Impact factor: 4.956

9.  Chemical space networks: a powerful new paradigm for the description of chemical space.

Authors:  Gerald M Maggiora; Jürgen Bajorath
Journal:  J Comput Aided Mol Des       Date:  2014-06-13       Impact factor: 3.686

10.  The Calculation of Molecular Structural Similarity: Principles and Practice.

Authors:  Peter Willett
Journal:  Mol Inform       Date:  2014-04-29       Impact factor: 3.353

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Journal:  J Cheminform       Date:  2017-03-09       Impact factor: 5.514

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