4.7 Article

Modelling and prediction of soil sorption coefficients of non-ionic organic pesticides by molecular descriptors

Journal

CHEMOSPHERE
Volume 41, Issue 5, Pages 763-777

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0045-6535(99)00463-4

Keywords

quantitative structure-property relationships; molecular descriptors; WHIM descriptors; genetic algorithm-variable subset selection; soil sorption coefficient

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Soil sorption coefficients (K-OC) of 185 non-ionic organic heterogeneous pesticides have been studied searching for quantitative structure-property relationships (QSPRs). The chemical description of pesticide structure has been made in terms of some molecular descriptors: count descriptors, topological indices, information indices, fragment-based descriptors and weighted holistic invariant molecular (WHIM) descriptors; these last are statistical indices describing size, shape, symmetry and atom distribution of molecules in the three-dimensional space. Three new topological indices derived from the electrotopological state indices of Kier and Hall were proposed. Multiple linear regression analysis was performed after previous selection of the descriptors mostly correlated to the response by Genetic Algorithms. The obtained results confirm the capability of the proposed approach to give predictive models for one of the most important partition properties, such as soil sorption coefficient (K-OC). (C) 2000 Elsevier Science Ltd. All rights reserved.

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