Literature DB >> 14641892

Prediction of human blood: air partition coefficient: a comparison of structure-based and property-based methods.

Subhash C Basak1, Denise Mills, Douglas M Hawkins, Hisham A El-Masri.   

Abstract

In recent years, there has been increased interest in the development and use of quantitative structure-activity/property relationship (QSAR/QSPR) models. For the most part, this is due to the fact that experimental data is sparse and obtaining such data is costly, while theoretical structural descriptors can be obtained quickly and inexpensively. In this study, three linear regression methods, viz. principal component regression (PCR), partial least squares (PLS), and ridge regression (RR), were used to develop QSPR models for the estimation of human blood:air partition coefficient (logPblood:air) for a group of 31 diverse low-molecular weight volatile chemicals from their computed molecular descriptors. In general, RR was found to be superior to PCR or PLS. Comparisons were made between models developed using parameters based solely on molecular structure and linear regression (LR) models developed using experimental properties, including saline:air partition coefficient (logPsaline:air) and olive oil:air partition coefficient (logPolive oil:air), as independent variables, indicating that the structure-property correlations are comparable to the property-property correlations. The best models, however, were those that used rat logPblood:air as the independent variable. Haloalkane subgroups were modeled separately for comparative purposes and, although models based on the congeneric compounds were superior, the models developed on the complete set of diverse compounds were of acceptable quality. The structural descriptors were placed into one of three classes based on level of complexity: topostructural (TS), topochemical (TC), or three-dimensional/geometrical (3D). Modeling was performed using the structural descriptor classes both in a hierarchical fashion and separately. The results indicate that highest quality structure-based models, in terms of descriptor classes, were those derived using TC descriptors.

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Year:  2003        PMID: 14641892     DOI: 10.1111/j.0272-4332.2003.00390.x

Source DB:  PubMed          Journal:  Risk Anal        ISSN: 0272-4332            Impact factor:   4.000


  3 in total

1.  On an aspect of calculated molecular descriptors in QSAR studies of quinolone antibacterials.

Authors:  Payel Ghosh; Megha Thanadath; Manish C Bagchi
Journal:  Mol Divers       Date:  2006-08-02       Impact factor: 2.943

2.  Predicting allergic contact dermatitis: a hierarchical structure-activity relationship (SAR) approach to chemical classification using topological and quantum chemical descriptors.

Authors:  Subhash C Basak; Denise Mills; Douglas M Hawkins
Journal:  J Comput Aided Mol Des       Date:  2008-03-13       Impact factor: 3.686

3.  Quantitative structure-activity relationship (QSAR) studies of quinolone antibacterials against M. fortuitum and M. smegmatis using theoretical molecular descriptors.

Authors:  Manish C Bagchi; Denise Mills; Subhash C Basak
Journal:  J Mol Model       Date:  2006-08-24       Impact factor: 1.810

  3 in total

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