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Molecular Pharmacology|July 11, 1998
Ligand specificity of the genetic variants of human alpha1-acid glycoprotein: generation of a three-dimensional quantitative structure-activity relationship model for drug binding to the A variantF Hervé, G Caron, J C Duché, et al.AAPS Pharmsci|December 14, 2001
Monoamine oxidase inhibitor properties of some benzazoles: structure-activity relationshipsT Grandi, F Sparatore, C Gnerre, et al.Biochemical Pharmacology|August 15, 1990
Toxication of MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) and analogs by monoamine oxidase. A structure-reactivity relationship studyG Maret, N el Tayar, P A Carrupt, et al.Pharmaceutical Research|November 8, 2001
The esterase-like activity of serum albumin may be due to cholinesterase contaminationN Chapuis, C Brühlmann, M Reist, et al.Journal of Medicinal Chemistry|April 1, 1991
Morphine 6-glucuronide and morphine 3-glucuronide as molecular chameleons with unexpected lipophilicityP A Carrupt, B Testa, A Bechalany, et al.The Journal of Pharmacy and Pharmacology|September 1, 1988
Influence of lipophilicity and chirality on the selectivity of ligands for beta 1- and beta 2-adrenoceptorsN el Tayar, B Testa, H van de Waterbeemd, et al.Journal of Pharmaceutical Sciences|August 1, 1991
Percutaneous penetration of drugs: a quantitative structure-permeability relationship studyN el Tayar, R S Tsai, B Testa, et al.Journal of the American Chemical Society|October 25, 2001
Generalization of ionic partition diagrams to lipophilic compounds and to biphasic systems with variable phase volume ratiosV Gobry, S Ulmeanu, F Reymond, et al.British Journal of Pharmacology|May 14, 1998
Evidence for the existence of [3H]-trimetazidine binding sites involved in the regulation of the mitochondrial permeability transition poreD Morin, A Elimadi, R Sapena, et al.Journal of Medicinal Chemistry|December 22, 2000
Inhibition of monoamine oxidases by functionalized coumarin derivatives: biological activities, QSARs, and 3D-QSARsC Gnerre, M Catto, F Leonetti, et al.Pageof 29