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C HANSCH

Showing results (31-40 of 197) with videos related to

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Journal 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 Hansch
Il Farmaco; Edizione Scientifica|January 1, 1979
QSAR of the inhibition of glyoxalase by S-substituted glutathionesC Silipo, C Hansch
Journal of Computer-Aided Molecular Design|October 1, 1991
The structure-activity relationship of inhibitors of serotonin uptake and receptor bindingC Hansch, J Caldwell
Journal of Medicinal Chemistry|July 1, 1974
Quantitative structure-activity relationship of reversible dihydrofolate reductase inhibitors. DiaminotriazinesC Hansch, C Silipo
SAR and QSAR in Environmental Research|January 1, 1995
Comparative QSAR: radical toxicity and scavenging. Two different sides of the same coinC Hansch, L Zhang
Journal of Pharmaceutical Sciences|January 1, 1972
Linear relationships between lipophilic character and biological activity of drugsC Hansch, W J Dunn
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 Hansch
Bioorganic & Medicinal Chemistry|October 13, 2001
Comparative QSAR studies on bibenzimidazoles and terbenzimidazoles inhibiting topoisomerase IS B Mekapati, C Hansch
Experientia|September 15, 1973
Correlation of physicochemical parameters and biological activity in steroids. 9Alpha-substituted corticol derivativesM E Wolff, C Hansch
Journal of Pharmaceutical Sciences|April 1, 1972
Relationship between lipophilic character and anesthetic activityW R Glave, C Hansch
Pageof 20

Showing results (31-40 of 197) with videos related to

Sort By:
Pageof 20
Journal 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 Hansch
Il Farmaco; Edizione Scientifica|January 1, 1979
QSAR of the inhibition of glyoxalase by S-substituted glutathionesC Silipo, C Hansch
Journal of Computer-Aided Molecular Design|October 1, 1991
The structure-activity relationship of inhibitors of serotonin uptake and receptor bindingC Hansch, J Caldwell
Journal of Medicinal Chemistry|July 1, 1974
Quantitative structure-activity relationship of reversible dihydrofolate reductase inhibitors. DiaminotriazinesC Hansch, C Silipo
SAR and QSAR in Environmental Research|January 1, 1995
Comparative QSAR: radical toxicity and scavenging. Two different sides of the same coinC Hansch, L Zhang
Journal of Pharmaceutical Sciences|January 1, 1972
Linear relationships between lipophilic character and biological activity of drugsC Hansch, W J Dunn
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 Hansch
Bioorganic & Medicinal Chemistry|October 13, 2001
Comparative QSAR studies on bibenzimidazoles and terbenzimidazoles inhibiting topoisomerase IS B Mekapati, C Hansch
Experientia|September 15, 1973
Correlation of physicochemical parameters and biological activity in steroids. 9Alpha-substituted corticol derivativesM E Wolff, C Hansch
Journal of Pharmaceutical Sciences|April 1, 1972
Relationship between lipophilic character and anesthetic activityW R Glave, C Hansch
Pageof 20