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Annual Review of Pharmacology and Toxicology|January 1, 1981
Structure-activity relationships and drug dispositionE J LienChemico-Biological Interactions|August 1, 1997
A comparative QSAR analysis of acetylcholinesterase inhibitors currently studied for the treatment of Alzheimer's diseaseM Recanatini, A Cavalli, C HanschScience (New York, N.Y.)|October 16, 1981
Oculomotor reaction time in dementia reflects degree of cerebral dysfunctionF J Pirozzolo, E C HanschChemico-Biological Interactions|January 1, 1985
Quantitative structure-activity relationships of cysteine hydrolases. Ficin hydrolysis of X-phenyl-N-methanesulfonyl glycinatesA Carotti, C Raguseo, C HanschBioorganic & Medicinal Chemistry|November 17, 2001
Possible allosteric effects in anticancer compoundsR Garg, A Kurup, C HanschMedicinal Research Reviews|January 3, 2001
Radical toxicity of phenols: a reference point for obtaining perspective in the formulation of QSARR Garg, S Kapur, C HanschJournal of Medicinal Chemistry|January 1, 1978
Structure-activity relationships in antitumor aniline mustardsA Panthananickal, C Hansch, A LeoBioorganic & Medicinal Chemistry|March 16, 2001
Searching for allosteric effects via QSARsC Hansch, R Garg, A KurupJournal of Medicinal Chemistry|November 1, 1984
Structure-activity relationship of the ficin hydrolysis of phenyl hippurates. Comparison with papain, actinidin, and bromelainA Carotti, G Casini, C HanschJournal of Medicinal Chemistry|October 1, 1979
Structure-activity relationship of aniline mustards acting against B-16 melanoma in miceA Panthananickal, C Hansch, A LeoPageof 19