Showing results (31-40 of 190) with videos related to
Sort By:
Pageof 19
Critical Reviews in Toxicology|April 17, 2001
Comparative QSAR: on the toxicology of the phenolic OH moietyR Garg, A Kurup, C HanschJournal of Medicinal Chemistry|May 1, 1976
Dependence of hydrophobicity of apolar molecules on their molecular volumeA Leo, C Hansch, P Y JowJournal 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 PanthananickalCritical Reviews in Toxicology|January 1, 1995
Comparative QSAR in toxicology: examples from teratology and cancer chemotherapy of aniline mustardsC Hansch, B R Telzer, L ZhangJournal of Pharmaceutical Sciences|July 1, 1975
Formulation of de novo substituent constants in correlation analysis: inhibition of dihydrofolate reductase by 2,4-diamino-5-(3,4-dichlorophenyl)-6-substituted pyrimidinesC Hansch, C Silipo, E E StellerChemico-Biological Interactions|January 1, 1988
Trypsin hydrolysis of X-phenyl hippuratesC D Selassie, M Chow, C HanschBioorganic & Medicinal Chemistry|September 8, 2000
Comparative QSAR studies on substituted bis-(acridines) and bis-(phenazines)-carboxamides: a new class of anticancer agentsR Garg, W A Denny, C HanschJournal of Medicinal Chemistry|April 1, 1982
A comparison of the inhibitory action of 5-(substituted-benzyl)-2,4-diaminopyrimidines on dihydrofolate reductase from chicken liver with that from bovine liverR Li, C Hansch, B T KaufmanJournal 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 Pharmaceutical Sciences|April 1, 1975
Selection of a reference partitioning system for drug design workR N Smith, C Hansch, M M AmesPageof 19