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Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|May 10, 2003
IARC carcinogens reported in cigarette mainstream smoke and their calculated log P valuesC J Smith, T A Perfetti, R Garg, et al.Toxicology Letters|September 1, 1995
The expanding role of quantitative structure-activity relationships (QSAR) in toxicologyC Hansch, D Hoekman, A Leo, et al.Archives of Biochemistry and Biophysics|November 1, 1983
The inhibition of alcohol dehydrogenase in vitro and in isolated hepatocytes by 4-substituted pyrazolesN W Cornell, C Hansch, K H Kim, et al.Biochimica Et Biophysica Acta|April 19, 1990
The structure-activity relationship of the papain hydrolysis of N-benzoylglycine estersC M Compadre, C Hansch, T E Klein, et al.Pharmaceutical Research|September 1, 1995
Hydrophobic contribution constants of amino acid residues to the hydrophobicities of oligopeptidesH Gao, F Wang, E J LienPharmaceutical Research|August 1, 1996
Correlation of physiochemical parameters to the hydrophobic contribution constants of amino acid residues in small peptidesD Palekar, M Shiue, E J LienJournal of Drug Targeting|January 1, 1993
Hydrophobicity of oligopeptides having un-ionizable side chainsH Gao, E J Lien, F WangBioorganic & Medicinal Chemistry|October 13, 2001
QSAR of anticancer compounds. Bis(11-oxo-11H-indeno[1,2-b]quinoline-6-carboxamides), bis(phenazine-1-carboxamides), and bis(naphthalimides)S B Mekapati, W A Denny, A Kurup, et al.Environmental and Molecular Mutagenesis|January 1, 1992
A QSAR investigation of the role of hydrophobicity in regulating mutagenicity in the Ames test: 1. Mutagenicity of aromatic and heteroaromatic amines in Salmonella typhimurium TA98 and TA100A K Debnath, G Debnath, A J Shusterman, et al.Chemico-Biological Interactions|July 21, 2000
Comparative QSAR evidence for a free-radical mechanism of phenol-induced toxicityC Hansch, S C McKarns, C J Smith, et al.Pageof 19