The expanding role of quantitative structure-activity relationships (QSAR) in toxicology.

[1]  A. Debnath,et al.  International Commission for Protection Against Environmental Mutagens and Carcinogens. The importance of the hydrophobic interaction in the mutagenicity of organic compounds. , 1994, Mutation research.

[2]  Peng Li,et al.  A comprehensive approach to database management of quantitative structure-activity relationships (QSAR) in chemistry and biology , 1994, 1994 Proceedings of the Twenty-Seventh Hawaii International Conference on System Sciences.

[3]  C. Hansch.  Quantitative structure-activity relationships and the unnamed science , 1993 .

[4]  L. Benet,et al.  Predictability of the covalent binding of acidic drugs in man. , 1993, Life sciences.

[5]  C. Hansch,et al.  Quantitative structure-activity relationships of cytochrome P-450. , 1993, Drug metabolism reviews.

[6]  E Novellino,et al.  Toward a quantitative comparative toxicology of organic compounds. , 1989, Critical reviews in toxicology.

[7]  C. Hansch,et al.  Molecular graphics and QSAR in the study of enzyme-ligand interactions. On the definition of bioreceptors , 1986 .

[8]  H Kubinyi,et al.  Lipophilicity and drug activity. , 1979, Progress in drug research. Fortschritte der Arzneimittelforschung. Progres des recherches pharmaceutiques.

[9]  W. Dunn,et al.  Chemicobiological interactions and the use of partition coefficients in their correlation. , 1974, Chemico-biological interactions.

[10]  W J Dunn,et al.  Linear relationships between lipophilic character and biological activity of drugs. , 1972, Journal of pharmaceutical sciences.

[11]  C. Hansch.  Quantitative approach to biochemical structure-activity relationships , 1969 .