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- W2013267718 abstract "A quantitative structure-activity relationship (QSAR) study for predicting the acute toxicity 96h - LC50 values of substituted anilines and phenols to carp is presented in this work. For this, the descriptors were obtained with DFT method at the B3LYP/6-311G** level using the Gaussian 03 software package. Afterwards the obtained parameters were taken as theoretical descriptors to establish a QSAR model for predicting -lgLC50. The model contains two variables, energy of the highest occupied molecular orbital (EHOMO) and energy of the lowest unoccupied molecular orbital (ELUMO), which suggest that the main effect on biological toxicity of phenols and anilines is the interaction of electrons between the molecules of organic chemicals. Besides, the model was further validated by variance inflation factors (VIF) and t-test, and show fine stabilities and predictive abilities, which can be used to predict -lgLC50 of these kinds of compounds." @default.
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- W2013267718 date "2013-02-01" @default.
- W2013267718 modified "2023-09-27" @default.
- W2013267718 title "QSAR Analyzes for the Predictive Toxicity of Substituted Phenols and Anilines to Fish (<i>carp</i>)" @default.
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- W2013267718 doi "https://doi.org/10.4028/www.scientific.net/amm.295-298.109" @default.
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