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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.
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.
The Journal of Pharmacology and Experimental Therapeutics|December 23, 1998
Three-dimensional quantitative structure activity relationship analyses of substrates for CYP2B6S Ekins, G Bravi, B J Ring, 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.
Drug Design and Delivery|December 1, 1987
Multivariate statistical analysis of L-dopa esters as potential anti-parkinsonian prodrugsH Van de Waterbeemd, B Testa, C Marrel, et al.
The Journal of Pharmacy and Pharmacology|October 1, 1987
L-dopa esters as potential prodrugs: effect on brain concentration of dopamine metabolites in reserpinized miceD R Cooper, C Marrel, H van de Waterbeemd, et al.
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