Literature DB >> 19434903

Toward novel universal descriptors: charge fingerprints.

Frank R Burden1, Mitchell J Polley, David A Winkler.   

Abstract

Although there are a myriad of molecular descriptors for QSAR described in the literature, many descriptors contain similar information as others or are information poor. Recent work has suggested that it may be possible to discover a relatively small pool of 'universal' descriptors from which subsets can be drawn to build a diverse variety of models. We describe a new type of descriptor of this type, the charge fingerprint. This descriptor family can build good QSAR models of a diverse range of physicochemical and biological properties and can be calculated quickly and easily. It appears to be useful for modeling large data sets and has potential for screening large virtual libraries.

Mesh:

Year:  2009        PMID: 19434903     DOI: 10.1021/ci800290h

Source DB:  PubMed          Journal:  J Chem Inf Model        ISSN: 1549-9596            Impact factor:   4.956


  5 in total

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Authors:  David A Winkler
Journal:  J Comput Aided Mol Des       Date:  2018-02-14       Impact factor: 3.686

2.  A multi-fingerprint browser for the ZINC database.

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Journal:  Nucleic Acids Res       Date:  2014-04-29       Impact factor: 16.971

3.  Prediction of PKCθ inhibitory activity using the Random Forest Algorithm.

Authors:  Ming Hao; Yan Li; Yonghua Wang; Shuwei Zhang
Journal:  Int J Mol Sci       Date:  2010-09-20       Impact factor: 5.923

4.  Prediction of kinase-inhibitor binding affinity using energetic parameters.

Authors:  Singaravelu Usha; Samuel Selvaraj
Journal:  Bioinformation       Date:  2016-06-15

5.  High-quality and universal empirical atomic charges for chemoinformatics applications.

Authors:  Stanislav Geidl; Tomáš Bouchal; Tomáš Raček; Radka Svobodová Vařeková; Václav Hejret; Aleš Křenek; Ruben Abagyan; Jaroslav Koča
Journal:  J Cheminform       Date:  2015-12-02       Impact factor: 5.514

  5 in total

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