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Chemico-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 LeoBiochimica Et Biophysica Acta|August 9, 1991
Separation of electronic and hydrophobic effects for the papain hydrolysis of substituted N-benzoylglycine estersC M Compadre, C Hansch, T E Klein, et al.Journal of Medicinal Chemistry|November 1, 1977
Quantitative structure-activity relationship of chymotrypsin-ligand interactionsC Hansch, C Grieco, C Silipo, et al.Journal of Medicinal Chemistry|January 1, 1977
Quantitative structure-activity relationships of antimalarial and dihydrofolate reductase inhibition by quinazolines and 5-substituted benzyl-2,4-diaminopyrimidinesC Hansch, J Y Fukunaga, P Y JowMolecular Pharmacology|May 1, 1985
A quantitative structure-activity relationship and molecular graphics study of carbonic anhydrase inhibitorsC Hansch, J McClarin, T Klein, et al.Journal of Chromatography|December 11, 1978
Determination of indicine N-oxide and indicine in plasma and urine by electron-capture gas-liquid chromatographyM M Ames, G PowisLeukemia|January 1, 1992
Selected pharmacologic characteristics of idarubicin and idarubicinolM M Ames, F SpreaficoPageof 35