Literature DB >> 16268758

An approach to determining applicability domains for QSAR group contribution models: an analysis of SRC KOWWIN.

Nina Nikolova-Jeliazkova1, Joanna Jaworska.   

Abstract

QSAR model predictions are most reliable if they come from the models applicability domain. The Setubal Workshop report provides a conceptual guidance for defining a (Q)SAR applicability domain. However, an operational definition is necessary for applying this guidance in practice. It should also permit the design of an automatic (computerised) procedure for determining a models applicability domain. This paper attempts to address this need for models that use a large number of descriptors (for example, group contribution-based models). The high dimensionality of these models imposes specific computational restrictions on estimating the interpolation region. The Syracuse Research Corporation KOWWIN model for prediction of the n-octanol/water partition coefficient is analysed as a case study. This is a linear regression model that uses 508 fragment counts and correction factors as descriptors, and is based on the group contribution approach. We conclude that the applicability domain estimation by descriptor ranges, combined with Principal Component rotation as a data pre-processing step, is an acceptable compromise between estimation accuracy and the amount of data in the training set.

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Year:  2005        PMID: 16268758     DOI: 10.1177/026119290503300510

Source DB:  PubMed          Journal:  Altern Lab Anim        ISSN: 0261-1929            Impact factor:   1.303


  7 in total

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Journal:  Methods Mol Biol       Date:  2013

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Authors:  Faizan Sahigara; Davide Ballabio; Roberto Todeschini; Viviana Consonni
Journal:  J Cheminform       Date:  2013-05-30       Impact factor: 5.514

4.  OPERA models for predicting physicochemical properties and environmental fate endpoints.

Authors:  Kamel Mansouri; Chris M Grulke; Richard S Judson; Antony J Williams
Journal:  J Cheminform       Date:  2018-03-08       Impact factor: 5.514

5.  Distributed Representation of Chemical Fragments.

Authors:  Suman K Chakravarti
Journal:  ACS Omega       Date:  2018-03-08

6.  Navigating the Minefield of Computational Toxicology and Informatics: Looking Back and Charting a New Horizon.

Authors:  Grace Patlewicz
Journal:  Front Toxicol       Date:  2020-06-25

7.  Mechanistic Chromatographic Column Characterization for the Analysis of Flavonoids Using Quantitative Structure-Retention Relationships Based on Density Functional Theory.

Authors:  Bogusław Buszewski; Petar Žuvela; Gulyaim Sagandykova; Justyna Walczak-Skierska; Paweł Pomastowski; Jonathan David; Ming Wah Wong
Journal:  Int J Mol Sci       Date:  2020-03-17       Impact factor: 5.923

  7 in total

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