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Journal of Medicinal Chemistry|October 1, 1979
Structure-activity relationship of aniline mustards acting against B-16 melanoma in miceA Panthananickal, C Hansch, A LeoJournal of Medicinal Chemistry|January 1, 1978
Structure-activity relationships in antitumor aniline mustardsA Panthananickal, C Hansch, A LeoJournal of Medicinal Chemistry|April 1, 1980
Mutagenicity of substituted (o-phenylenediamine)platinum dichloride in the Ames test. A quantitative structure-activity analysisC Hansch, B H Venger, A PanthananickalJournal of Medicinal Chemistry|July 1, 1981
A comparison of mutagenic and carcinogenic activities of aniline mustardsA Leo, A Panthananickal, C Hansch, et al.Journal of Medicinal Chemistry|March 1, 1982
Potential antitumor agents. 36. Quantitative relationships between experimental antitumor activity, toxicity, and structure for the general class of 9-anilinoacridine antitumor agentsW A Denny, B F Cain, G J Atwell, et al.Journal of Medicinal Chemistry|May 1, 1976
Dependence of hydrophobicity of apolar molecules on their molecular volumeA Leo, C Hansch, P Y JowJournal of Pharmaceutical Sciences|September 1, 1987
Hydrophobicity and central nervous system agents: on the principle of minimal hydrophobicity in drug designC Hansch, J P Björkroth, A LeoJournal of Medicinal Chemistry|September 1, 1975
Calculation of hydrophobic constant (log P) from pi and f constantsA Leo, P Y Jow, C Silipo, et al.Toxicology Letters|September 1, 1995
The expanding role of quantitative structure-activity relationships (QSAR) in toxicologyC Hansch, D Hoekman, A Leo, et al.Journal of Medicinal Chemistry|October 1, 1980
Antitumor structure-activity relations. Nitrosoureas vs. L-1210 leukemiaC Hansch, A Leo, C Schmidt, et al.Pageof 34