R N Smith|C Hansch|M M Ames - JoVE Visualize

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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.

The Journal of Biological Chemistry|January 10, 1978

Tyrosine hydroxylase. Activation by protein phosphorylation and end product inhibitionM M Ames, P Lerner, W Lovenberg

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.

Bioorganic & 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.

Journal of Medicinal Chemistry|June 1, 1979

Quantitative structure-activity relationship of 5-(X-benzyl)-2,4-diaminopyrimidines inhibiting bovine liver dihydrofolate reductaseJ M Blaney, S W Dietrich, M A Reynolds, et al.

Pageof 35

Showing results (71-80 of 343) with videos related to

Sort By:

Pageof 35

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.

The Journal of Biological Chemistry|January 10, 1978

Tyrosine hydroxylase. Activation by protein phosphorylation and end product inhibitionM M Ames, P Lerner, W Lovenberg

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.

Bioorganic & 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.

Journal of Medicinal Chemistry|June 1, 1979

Quantitative structure-activity relationship of 5-(X-benzyl)-2,4-diaminopyrimidines inhibiting bovine liver dihydrofolate reductaseJ M Blaney, S W Dietrich, M A Reynolds, et al.

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