Huuskonen Jarmo
Division of Pharmaceutical Chemistry, Department of Pharmacy, PO Box 56, 00014 University of Helsinki, Finland.
Environ Toxicol Chem. 2003 Apr;22(4):816-20.
A group contribution approach based on atom-type electrotopological state indices for predicting the soil sorption coefficient (log KOC) of a diverse set of 201 organic pesticides is presented. Using a training set of 143 compounds, for which the log KOC values were in the range from 0.42 to 5.31, multiple linear regression (MLR) and artificial neural networks were used to build the models. The models were validated using two test sets of 20 and 38 chemicals not included in the training set. The statistics for a linear model with 12 structural parameters were, in test set 1, r2 = 0.79, s = 0.45 and, in test set 2, r2 = 0.74, s = 0.65. These results clearly show that soil sorption coefficients can be accurately and rapidly estimated from easily calculated structural parameters.
提出了一种基于原子类型电子拓扑状态指数的基团贡献法,用于预测201种不同有机农药的土壤吸附系数(log KOC)。使用143种化合物的训练集(其log KOC值范围为0.42至5.31),采用多元线性回归(MLR)和人工神经网络建立模型。使用训练集中未包含的20种和38种化学品的两个测试集对模型进行验证。在测试集1中,具有12个结构参数的线性模型的统计数据为r2 = 0.79,s = 0.45;在测试集2中,r2 = 0.74,s = 0.65。这些结果清楚地表明,可以根据易于计算的结构参数准确快速地估算土壤吸附系数。