Quantitative structure-activity relations. 7. The bilinear model, a new model for nonlinear dependence of biological activity on hydrophobic character
- 1 May 1977
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 20 (5), 625-629
- https://doi.org/10.1021/jm00215a002
Abstract
The bilinear model, log 1/C = a log P - b log (.beta.P + 1) + c, a new model for nonlinear dependence of pharmaceutical biological activity on hydrophobic character, is applied to 57 data sets of biological activity values in homologous series. From a comparison of the statistical parameters and the residuals obtained with the bilinear model and the parabolic model, the superiority of the bilinear model for a precise quantitative description of both linear and nonlinear parts of structure-activity relationships can be derived; the bilinear model explains the particular effect that in homologous series the relationship between biological activity and hydrophobic character is strictly linear for the lower members while for higher members this relationship is nonlinear.This publication has 2 references indexed in Scilit:
- Theoretical model-based equations for the linear free energy relations of the biological activity of ionizable substances. 1. Equilibrium-controlled potencyJournal of Medicinal Chemistry, 1976
- Zur Theorie der AlkoholnarkoseNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1899