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C Hansch

Showing results (151-160 of 197) with videos related to

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Critical Reviews in Toxicology|January 1, 1989
Toward a quantitative comparative toxicology of organic compoundsC Hansch, D Kim, A J Leo, et al.
Environmental and Molecular Mutagenesis|January 1, 1990
LUMO energies and hydrophobicity as determinants of mutagenicity by nitroaromatic compounds in Salmonella typhimuriumR L Lopez de Compadre, A K Debnath, A J Shusterman, et al.
Journal of Medicinal Chemistry|March 1, 1984
Comparative structure-activity relationships of antifolate triazines inhibiting murine tumor cells sensitive and resistant to methotrexateC D Selassie, C Hansch, T A Khwaja, et al.
Journal of Medicinal Chemistry|July 1, 1981
A comparison of mutagenic and carcinogenic activities of aniline mustardsA Leo, A Panthananickal, C Hansch, et al.
Molecular Pharmacology|April 1, 1986
Quantitative structure-activity relationships and molecular graphics in ligand receptor interactions: amidine inhibition of trypsinM Recanatini, T Klein, C Z Yang, et al.
Experientia. Supplementum|January 1, 1976
Quantitation of chemical and biological effects in steroids by Hansch-type and molecular orbital calculationsM E Wolff, C Hansch, P A Kollman, et al.
Journal of Medicinal Chemistry|November 1, 1980
Inhibition of dihydrofolate reductase. 3. 4.6-Diamino-1,2-dihydro-2,2-dimethyl-1-(2-substituted-phenyl)-s-triazine inhibition of bovine liver and mouse tumor enzymesK H Kim, S W Dietrich, C Hansch, et al.
Journal of Medicinal Chemistry|November 1, 1980
Quantitative structure-selectivity relationships. Comparison of the inhibition of Escherichia coli and bovine liver dihydrofolate reductase by 5-(substituted-benzyl)-2,4-diaminopyrimidinesS W Dietrich, J M Blaney, M A Reynolds, et al.
Journal of Medicinal Chemistry|December 1, 1985
Quantitative structure-activity relationship of antifolate inhibition of bacteria cell cultures resistant and sensitive to methotrexateE A Coats, C S Genther, C D Selassie, et al.
Archives of Biochemistry and Biophysics|February 15, 1984
Papain hydrolysis of X-phenyl-N-methanesulfonyl glycinates: a quantitative structure-activity relationship and molecular graphics analysisA Carotti, R N Smith, S Wong, et al.
Pageof 20

Showing results (151-160 of 197) with videos related to

Sort By:
Pageof 20
Critical Reviews in Toxicology|January 1, 1989
Toward a quantitative comparative toxicology of organic compoundsC Hansch, D Kim, A J Leo, et al.
Environmental and Molecular Mutagenesis|January 1, 1990
LUMO energies and hydrophobicity as determinants of mutagenicity by nitroaromatic compounds in Salmonella typhimuriumR L Lopez de Compadre, A K Debnath, A J Shusterman, et al.
Journal of Medicinal Chemistry|March 1, 1984
Comparative structure-activity relationships of antifolate triazines inhibiting murine tumor cells sensitive and resistant to methotrexateC D Selassie, C Hansch, T A Khwaja, et al.
Journal of Medicinal Chemistry|July 1, 1981
A comparison of mutagenic and carcinogenic activities of aniline mustardsA Leo, A Panthananickal, C Hansch, et al.
Molecular Pharmacology|April 1, 1986
Quantitative structure-activity relationships and molecular graphics in ligand receptor interactions: amidine inhibition of trypsinM Recanatini, T Klein, C Z Yang, et al.
Experientia. Supplementum|January 1, 1976
Quantitation of chemical and biological effects in steroids by Hansch-type and molecular orbital calculationsM E Wolff, C Hansch, P A Kollman, et al.
Journal of Medicinal Chemistry|November 1, 1980
Inhibition of dihydrofolate reductase. 3. 4.6-Diamino-1,2-dihydro-2,2-dimethyl-1-(2-substituted-phenyl)-s-triazine inhibition of bovine liver and mouse tumor enzymesK H Kim, S W Dietrich, C Hansch, et al.
Journal of Medicinal Chemistry|November 1, 1980
Quantitative structure-selectivity relationships. Comparison of the inhibition of Escherichia coli and bovine liver dihydrofolate reductase by 5-(substituted-benzyl)-2,4-diaminopyrimidinesS W Dietrich, J M Blaney, M A Reynolds, et al.
Journal of Medicinal Chemistry|December 1, 1985
Quantitative structure-activity relationship of antifolate inhibition of bacteria cell cultures resistant and sensitive to methotrexateE A Coats, C S Genther, C D Selassie, et al.
Archives of Biochemistry and Biophysics|February 15, 1984
Papain hydrolysis of X-phenyl-N-methanesulfonyl glycinates: a quantitative structure-activity relationship and molecular graphics analysisA Carotti, R N Smith, S Wong, et al.
Pageof 20