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Drug Intelligence & Clinical Pharmacy|May 1, 1982
Dihydrofolate reductase inhibition. A study in the use of X-ray crystallography, molecular graphics, and quantitative structure-activity relations in drug designC HanschJournal of Medicinal Chemistry|January 1, 1976
Correlation analysis of Baker's studies on enzyme inhibition. 1. Guanine deaminase, xanthine oxidase, dihydrofolate reductase, and complementC Silipo, C HanschThe Journal of Pharmacy and Pharmacology|August 1, 1990
The relative dependence of calcium antagonists and neuroleptics binding to brain and heart receptors on drug lipophilicityW Rojratanakiat, C HanschIl Farmaco; Edizione Scientifica|January 1, 1975
The structure-activity relationship of 9-(X-phenyl)guanine inhibitors of xanthine oxidaseC Silipo, C HanschJournal of Medicinal Chemistry|January 1, 1976
Correlation analysis of Baker's studies on enzyme inhibition. 2. Chymotrypsin, trypsin, thymidine phosphorylase, uridine phosphorylase, thymidylate synthetase, cytosine nucleoside deaminase, dihydrofolate reductase, malate dehydrogenase, glutamate dehydrogenase, lactate dehydrogenase, and glyceraldehyde-phosphate dehydrogenaseM Yoshimoto, C HanschIl Farmaco; Edizione Scientifica|January 1, 1979
QSAR of the inhibition of glyoxalase by S-substituted glutathionesC Silipo, C HanschJournal of Computer-Aided Molecular Design|October 1, 1991
The structure-activity relationship of inhibitors of serotonin uptake and receptor bindingC Hansch, J CaldwellSAR and QSAR in Environmental Research|January 1, 1995
Comparative QSAR: radical toxicity and scavenging. Two different sides of the same coinC Hansch, L ZhangJournal of Medicinal Chemistry|June 1, 1978
Antitumor 1-(X-aryl)-3,3-dialkyltriazenes. 1. Quantitative structure-activity relationships vs. L1210 leukemia in miceG J Hatheway, C Hansch, K H Kim, et al.Chemical Research in Toxicology|May 1, 1993
The importance of hydrophobicity in the mutagenicity of methanesulfonic acid esters with Salmonella typhimurium TA100A K Debnath, C HanschPageof 35