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Journal of Medicinal Chemistry
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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 dehydrogenase
M Yoshimoto, C Hansch
Il Farmaco; Edizione Scientifica
|
January 1, 1979
QSAR of the inhibition of glyoxalase by S-substituted glutathiones
C Silipo, C Hansch
Journal of Computer-Aided Molecular Design
|
October 1, 1991
The structure-activity relationship of inhibitors of serotonin uptake and receptor binding
C Hansch, J Caldwell
Journal of Medicinal Chemistry
|
July 1, 1974
Quantitative structure-activity relationship of reversible dihydrofolate reductase inhibitors. Diaminotriazines
C Hansch, C Silipo
SAR and QSAR in Environmental Research
|
January 1, 1995
Comparative QSAR: radical toxicity and scavenging. Two different sides of the same coin
C Hansch, L Zhang
Journal of Pharmaceutical Sciences
|
January 1, 1972
Linear relationships between lipophilic character and biological activity of drugs
C 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 TA100
A K Debnath, C Hansch
Bioorganic & Medicinal Chemistry
|
October 13, 2001
Comparative QSAR studies on bibenzimidazoles and terbenzimidazoles inhibiting topoisomerase I
S B Mekapati, C Hansch
Experientia
|
September 15, 1973
Correlation of physicochemical parameters and biological activity in steroids. 9Alpha-substituted corticol derivatives
M E Wolff, C Hansch
Journal of Pharmaceutical Sciences
|
April 1, 1972
Relationship between lipophilic character and anesthetic activity
W R Glave, C Hansch
Page
of 20
Search research articles
Search
Showing results (31-40 of 197) with videos related to
Sort By:
Page
of 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 dehydrogenase
M Yoshimoto, C Hansch
Il Farmaco; Edizione Scientifica
|
January 1, 1979
QSAR of the inhibition of glyoxalase by S-substituted glutathiones
C Silipo, C Hansch
Journal of Computer-Aided Molecular Design
|
October 1, 1991
The structure-activity relationship of inhibitors of serotonin uptake and receptor binding
C Hansch, J Caldwell
Journal of Medicinal Chemistry
|
July 1, 1974
Quantitative structure-activity relationship of reversible dihydrofolate reductase inhibitors. Diaminotriazines
C Hansch, C Silipo
SAR and QSAR in Environmental Research
|
January 1, 1995
Comparative QSAR: radical toxicity and scavenging. Two different sides of the same coin
C Hansch, L Zhang
Journal of Pharmaceutical Sciences
|
January 1, 1972
Linear relationships between lipophilic character and biological activity of drugs
C 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 TA100
A K Debnath, C Hansch
Bioorganic & Medicinal Chemistry
|
October 13, 2001
Comparative QSAR studies on bibenzimidazoles and terbenzimidazoles inhibiting topoisomerase I
S B Mekapati, C Hansch
Experientia
|
September 15, 1973
Correlation of physicochemical parameters and biological activity in steroids. 9Alpha-substituted corticol derivatives
M E Wolff, C Hansch
Journal of Pharmaceutical Sciences
|
April 1, 1972
Relationship between lipophilic character and anesthetic activity
W R Glave, C Hansch
Page
of 20