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C Hansch

Showing results (111-120 of 197) with videos related to

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Journal of Medicinal Chemistry|June 1, 1975
Partition coefficients and the structure-activity relationship of the anesthetic gasesC Hansch, A Vittoria, C Silipo, et al.
Chemico-Biological Interactions|January 1, 1992
The structure-activity relationship of skin carcinogenicity of aromatic hydrocarbons and heterocyclesL Zhang, K Sannes, A J Shusterman, et al.
Chemico-Biological Interactions|January 27, 1999
Quantitative structure-activity relationships (QSAR) for 9-anilinoacridines: a comparative analysisH Gao, W A Denny, R Garg, et al.
Journal of Medicinal Chemistry|June 1, 1978
Antitumor 1-(X-aryl)-3,3-dialkyltriazenes. 2. On the role of correlation analysis in decision making in drug modification. Toxicity quantitative structure-activity relationships of 1-(X-phenyl)-3,3-dialkyltriazenes in miceC Hansch, G J Hatheway, F R Quinn, et al.
Journal of Medicinal Chemistry|January 1, 1991
On the optimization of hydrophobic and hydrophilic substituent interactions of 2,4-diamino-5-(substituted-benzyl)pyrimidines with dihydrofolate reductaseC D Selassie, R L Li, M Poe, et al.
Current Problems in Dermatology|January 1, 1995
Quantitative structure-activity relationship and cytotoxicityN K Mize, J A Johnson, C Hansch, et al.
Archives of Biochemistry and Biophysics|May 1, 1979
The use of triazine inhibitors in mapping the active site region of Lactobacillus casei dihydrofolate reductaseS W Dietrich, R N Smith, S Brendler, et al.
Journal of Medicinal Chemistry|November 1, 1984
Actinidin hydrolysis of substituted-phenyl hippurates: a quantitative structure-activity relationship and graphics comparison with hydrolysis by papainA Carotti, C Hansch, M M Mueller, et al.
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.
Pageof 20

Showing results (111-120 of 197) with videos related to

Sort By:
Pageof 20
Journal of Medicinal Chemistry|June 1, 1975
Partition coefficients and the structure-activity relationship of the anesthetic gasesC Hansch, A Vittoria, C Silipo, et al.
Chemico-Biological Interactions|January 1, 1992
The structure-activity relationship of skin carcinogenicity of aromatic hydrocarbons and heterocyclesL Zhang, K Sannes, A J Shusterman, et al.
Chemico-Biological Interactions|January 27, 1999
Quantitative structure-activity relationships (QSAR) for 9-anilinoacridines: a comparative analysisH Gao, W A Denny, R Garg, et al.
Journal of Medicinal Chemistry|June 1, 1978
Antitumor 1-(X-aryl)-3,3-dialkyltriazenes. 2. On the role of correlation analysis in decision making in drug modification. Toxicity quantitative structure-activity relationships of 1-(X-phenyl)-3,3-dialkyltriazenes in miceC Hansch, G J Hatheway, F R Quinn, et al.
Journal of Medicinal Chemistry|January 1, 1991
On the optimization of hydrophobic and hydrophilic substituent interactions of 2,4-diamino-5-(substituted-benzyl)pyrimidines with dihydrofolate reductaseC D Selassie, R L Li, M Poe, et al.
Current Problems in Dermatology|January 1, 1995
Quantitative structure-activity relationship and cytotoxicityN K Mize, J A Johnson, C Hansch, et al.
Archives of Biochemistry and Biophysics|May 1, 1979
The use of triazine inhibitors in mapping the active site region of Lactobacillus casei dihydrofolate reductaseS W Dietrich, R N Smith, S Brendler, et al.
Journal of Medicinal Chemistry|November 1, 1984
Actinidin hydrolysis of substituted-phenyl hippurates: a quantitative structure-activity relationship and graphics comparison with hydrolysis by papainA Carotti, C Hansch, M M Mueller, et al.
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.
Pageof 20