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Medicinal 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 LeoCritical 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 StellerPageof 35