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Journal of Medicinal Chemistry
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April 1, 1982
A comparison of the inhibitory action of 5-(substituted-benzyl)-2,4-diaminopyrimidines on dihydrofolate reductase from chicken liver with that from bovine liver
R Li, C Hansch, B T Kaufman
Journal of Medicinal Chemistry
|
November 1, 1977
Inhibition of Lactobacillus casei thymidylate synthetase by 5-substituted 2'-deoxyuridylates. Preliminary quantitative structure-activity relationship
Y Wataya, D V Santi, C Hansch
Journal of Pharmaceutical Sciences
|
September 1, 1987
Hydrophobicity and central nervous system agents: on the principle of minimal hydrophobicity in drug design
C Hansch, J P Björkroth, A Leo
Journal of Medicinal Chemistry
|
August 1, 1972
Binding of apolar molecules by serum albumin
J M Vandenbelt, C Hansch, C Church
Journal of Pharmaceutical Sciences
|
April 1, 1975
Selection of a reference partitioning system for drug design work
R N Smith, C Hansch, M M Ames
Cancer Chemotherapy Reports
|
August 1, 1972
Quantitative structure-activity relationships of antineoplastic drugs: nitrosoureas and triazenoimidazoles
C Hansch, N Smith, R Engle, et al.
Journal of the American Chemical Society
|
September 19, 1973
Structure-activity relationship in benzamides inhibiting alochol dehydrogenase
C Hansch, K H Kim, R H Sarma
Journal of Medicinal Chemistry
|
November 1, 1973
Strategy in drug design. Cluster analysis as an aid in the selection of substituents
C Hansch, S H Unger, A B Forsythe
Journal of Medicinal Chemistry
|
November 1, 1977
Quantitative structure-activity relationship of chymotrypsin-ligand interactions
C Hansch, C Grieco, C Silipo, et al.
Physiological Chemistry and Physics
|
January 1, 1975
Kinetics and thermodynamics of the slow hydrophobic deactivation of alpha-chymotrypsin
R N Smith, T P Poindexter, C Hansch
Page
of 20
Search research articles
Search
Showing results (81-90 of 197) with videos related to
Sort By:
Page
of 20
Journal of Medicinal Chemistry
|
April 1, 1982
A comparison of the inhibitory action of 5-(substituted-benzyl)-2,4-diaminopyrimidines on dihydrofolate reductase from chicken liver with that from bovine liver
R Li, C Hansch, B T Kaufman
Journal of Medicinal Chemistry
|
November 1, 1977
Inhibition of Lactobacillus casei thymidylate synthetase by 5-substituted 2'-deoxyuridylates. Preliminary quantitative structure-activity relationship
Y Wataya, D V Santi, C Hansch
Journal of Pharmaceutical Sciences
|
September 1, 1987
Hydrophobicity and central nervous system agents: on the principle of minimal hydrophobicity in drug design
C Hansch, J P Björkroth, A Leo
Journal of Medicinal Chemistry
|
August 1, 1972
Binding of apolar molecules by serum albumin
J M Vandenbelt, C Hansch, C Church
Journal of Pharmaceutical Sciences
|
April 1, 1975
Selection of a reference partitioning system for drug design work
R N Smith, C Hansch, M M Ames
Cancer Chemotherapy Reports
|
August 1, 1972
Quantitative structure-activity relationships of antineoplastic drugs: nitrosoureas and triazenoimidazoles
C Hansch, N Smith, R Engle, et al.
Journal of the American Chemical Society
|
September 19, 1973
Structure-activity relationship in benzamides inhibiting alochol dehydrogenase
C Hansch, K H Kim, R H Sarma
Journal of Medicinal Chemistry
|
November 1, 1973
Strategy in drug design. Cluster analysis as an aid in the selection of substituents
C Hansch, S H Unger, A B Forsythe
Journal of Medicinal Chemistry
|
November 1, 1977
Quantitative structure-activity relationship of chymotrypsin-ligand interactions
C Hansch, C Grieco, C Silipo, et al.
Physiological Chemistry and Physics
|
January 1, 1975
Kinetics and thermodynamics of the slow hydrophobic deactivation of alpha-chymotrypsin
R N Smith, T P Poindexter, C Hansch
Page
of 20