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Journal of Pharmaceutical Sciences|April 1, 1975
Selection of a reference partitioning system for drug design workR N Smith, C Hansch, M M Ames
Physiological Chemistry and Physics|January 1, 1975
Kinetics and thermodynamics of the slow hydrophobic deactivation of alpha-chymotrypsinR N Smith, T P Poindexter, C Hansch
Molecular Pharmacology|November 1, 1983
Thiopurine methyltransferase. Aromatic thiol substrates and inhibition by benzoic acid derivativesL C Woodson, M M Ames, C D Selassie, et al.
Molecular Pharmacology|December 1, 1987
Human and rat liver phenol sulfotransferase: structure-activity relationships for phenolic substratesN R Campbell, J A Van Loon, R S Sundaram, 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 analysisA Carotti, R N Smith, S Wong, et al.
Journal of Medicinal Chemistry|March 1, 1986
Thiopurine methyltransferase: structure-activity relationships for benzoic acid inhibitors and thiophenol substratesM M Ames, C D Selassie, L C Woodson, et al.
The Science of the Total Environment|December 1, 1991
Structure-activity relationships of chemical mutagens and carcinogensC Hansch
Il Farmaco; Edizione Scientifica|January 1, 1979
QSAR in cancer chemotherapyC Hansch
Il Farmaco; Edizione Scientifica|August 1, 1979
The interaction of ligands with enzymes. A starting point in drug designC Hansch
Journal of Medicinal Chemistry|January 1, 1976
On the structure of medicinal chemistryC Hansch
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