出 处:《Chinese Journal of Structural Chemistry》2013年第3期387-395,共9页结构化学(英文)
基 金:Supported by the NNSF of China (No. 20737001);Program for Environment Protection in Jiangsu Province (201140)
摘 要:Octanol/water partition coefficient (Kow) is a crucial property for evaluating the environmental behavior and fate of organic compound. Herein, some quantitative structure-property relationship (QSPR) studies were performed to estimate and predict the lgK ow of substituted anilines. 2D method (multiple linear regression, MLR) and 3D method (comparative molecular field analysis, CoMFA) were applied in this study. Successful 2D and 3D models yielded the correlation coefficient (R2) values of 0.981 and 0.966 and the Leave-One-Out (LOO) cross-validated correlation coefficient (q2) values of 0.933 and 0.820, respectively. The developed models have a highly predictive ability in both internal and external validation. In addition, the results were interpreted in terms of physical and chemical meanings of descriptors and field contribution maps. It showed that the steric and electrostatic properties are the primary factors that govern the lgK ow of substituted anilines. The information obtained from the QSPR models would be helpful to the interpretation of structural features pertinent to the lgK ow of substituted anilines, which may be helpful in estimating the organic compounds' potential harm to the environment.Octanol/water partition coefficient (Kow) is a crucial property for evaluating the environmental behavior and fate of organic compound. Herein, some quantitative structure-property relationship (QSPR) studies were performed to estimate and predict the lgK ow of substituted anilines. 2D method (multiple linear regression, MLR) and 3D method (comparative molecular field analysis, CoMFA) were applied in this study. Successful 2D and 3D models yielded the correlation coefficient (R2) values of 0.981 and 0.966 and the Leave-One-Out (LOO) cross-validated correlation coefficient (q2) values of 0.933 and 0.820, respectively. The developed models have a highly predictive ability in both internal and external validation. In addition, the results were interpreted in terms of physical and chemical meanings of descriptors and field contribution maps. It showed that the steric and electrostatic properties are the primary factors that govern the lgK ow of substituted anilines. The information obtained from the QSPR models would be helpful to the interpretation of structural features pertinent to the lgK ow of substituted anilines, which may be helpful in estimating the organic compounds' potential harm to the environment.
关 键 词:octanol/water partition coefficient substituted anilines quantitative structure- property relationship multiple linear regression comparative molecular field analysis
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