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- W2113235554 abstract "Our semiempirical method of calculating log P, which uses a linear combination of various combinations of descriptors based on the AM1-optimized geometry of the molecule, has been applied to a set of 38 substituted phenols and has been shown to be successful in providing a better quantitative structure-activity relationship (QSAR) than that of the Hansch-type approach in a study of the inhibitory activity of substituted phenols on Bacillus subtilis spore germination. This model shows that the calculated partition coefficient, the geometrical descriptors, and electronic effects are the major factors determining the biological activity. © 1994 John Wiley & Sons, Inc." @default.
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- W2113235554 date "1994-02-12" @default.
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- W2113235554 title "Quantitative structure-inhibitory activity relationships of substituted phenols onbacillus subtilis spore germination" @default.
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- W2113235554 doi "https://doi.org/10.1002/qua.560520714" @default.
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