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Progress in Drug Research. Fortschritte Der Arzneimittelforschung. Progres Des Recherches Pharmaceutiques|June 17, 2000
Caco-2 cell permeability vs human gastrointestinal absorption: QSPR analysisS Ren, E J LienJournal of Clinical and Hospital Pharmacy|December 1, 1981
Quantitative structure activity relationships (QSAR) of lipophilic acids and related compounds on bacterial and mammalian cellsA T'Ang, E J LienJournal of Medicinal Chemistry|May 1, 1981
Quantitative structure-selectivity relationships. Comparison of the inhibition of Escherichia coli and bovine liver dihydrofolate reductase by 5-(substituted-benzyl)-2,4-diaminopyrimidinesR L Li, S W Dietrich, C HanschMutation Research|November 14, 1997
QSAR treatment of multiple toxicities: the mutagenicity and cytotoxicity of quinolinesC J Smith, C Hansch, M J MortonJournal of Medicinal Chemistry|May 1, 1976
Inhibition of dihydrofolate reductase. Structure-activity correlations of quinazolinesJ Y Fukunaga, C Hansch, E E StellerJournal of Medicinal Chemistry|July 1, 1990
Structure-activity relationships of antineoplastic agents in multidrug resistanceC D Selassie, C Hansch, T A KhwajaMutation Research|July 1, 1992
Mutagenicity of quinolines in Salmonella typhimurium TA100. A QSAR study based on hydrophobicity and molecular orbital determinantsA K Debnath, R L de Compadre, C HanschBiochemical Pharmacology|February 15, 1986
Induction of cytochrome P-450 by alcohols and 4-substituted pyrazoles. Comparison of structure-activity relationshipsJ Sinclair, N W Cornell, L Zaitlin, et al.Journal of Pharmaceutical Sciences|June 1, 1980
Effects of different buffer species on partition coefficients of drugs used in quantitative structure-activity relationshipsP H Wang, E J LienResearch Communications in Chemical Pathology and Pharmacology|September 1, 1980
QSAR of acetylchol inesterase inhibitors: a reexamination of the role of charge-transferC T Su, E J LienPageof 19