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Journal of Medicinal Chemistry
|
July 1, 1981
A comparison of mutagenic and carcinogenic activities of aniline mustards
A Leo, A Panthananickal, C Hansch, et al.
Circulation
|
June 23, 2010
Images in cardiovascular medicine. Spontaneous rupture of the right coronary artery
Andreas Hansch, Stefan Betge, Alexander Pfeil, et al.
Plant Signaling & Behavior
|
January 15, 2020
Brassinosteroids and sucrose transport in mycorrhizal tomato plants
Franziska Hansch, Hannah Jaspar, Lea von Sivers, et al.
Molecular Pharmacology
|
April 1, 1986
Quantitative structure-activity relationships and molecular graphics in ligand receptor interactions: amidine inhibition of trypsin
M 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 calculations
M 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 enzymes
K H Kim, S W Dietrich, C Hansch, et al.
Bioorganic & Medicinal Chemistry
|
January 23, 2003
Quantitative structure-activity relationships of phenolic compounds causing apoptosis
Corwin Hansch, Benjamin Bonavida, Ali R Jazirehi, 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-diaminopyrimidines
S 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 methotrexate
E 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 analysis
A Carotti, R N Smith, S Wong, et al.
Page
of 39
Search research articles
Search
Showing results (261-270 of 383) with videos related to
Sort By:
Page
of 39
Journal of Medicinal Chemistry
|
July 1, 1981
A comparison of mutagenic and carcinogenic activities of aniline mustards
A Leo, A Panthananickal, C Hansch, et al.
Circulation
|
June 23, 2010
Images in cardiovascular medicine. Spontaneous rupture of the right coronary artery
Andreas Hansch, Stefan Betge, Alexander Pfeil, et al.
Plant Signaling & Behavior
|
January 15, 2020
Brassinosteroids and sucrose transport in mycorrhizal tomato plants
Franziska Hansch, Hannah Jaspar, Lea von Sivers, et al.
Molecular Pharmacology
|
April 1, 1986
Quantitative structure-activity relationships and molecular graphics in ligand receptor interactions: amidine inhibition of trypsin
M 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 calculations
M 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 enzymes
K H Kim, S W Dietrich, C Hansch, et al.
Bioorganic & Medicinal Chemistry
|
January 23, 2003
Quantitative structure-activity relationships of phenolic compounds causing apoptosis
Corwin Hansch, Benjamin Bonavida, Ali R Jazirehi, 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-diaminopyrimidines
S 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 methotrexate
E 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 analysis
A Carotti, R N Smith, S Wong, et al.
Page
of 39