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- W4311150413 abstract "Toxicity data for the 50% growth inhibitory concentration against Tetrahymena pyriformis pCIC50 = -logCIC50 for 85 phenols substituted were obtained experimentally. Log (CIC50)-1 along with the hydrophobicity, the logarithm of the 1-octanol/water partition coefficient (log Kow), and R2u (GETAWAY descriptors). The entire data set was randomly split into a training set (60chemicals) used to establish the QSAR model, and a test set (25 chemicals) for statistical external validation The descriptors models were selected from an extensive set of several descriptors (topological, geometrical and quantum). Quantitative structure-activity/property (QSAR / The values of the statistical parameters obtained from the multiple linear regression analysis (R²=95.5%, Q²=95.01%, S=0.157, F=604.34, P=0, SDEC=0.153, SDEP=0.161, Q²ext=95.96%, SDEPext=0.153) testify to the good fit of the model." @default.
- W4311150413 created "2022-12-23" @default.
- W4311150413 creator A5077940061 @default.
- W4311150413 date "2022-11-14" @default.
- W4311150413 modified "2023-10-04" @default.
- W4311150413 title "Predictive QSAR models for the toxicity of Phenols" @default.
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- W4311150413 doi "https://doi.org/10.52711/0974-4150.2022.00076" @default.
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