Drug Lipophilicity in QSAR Practice: I. A Comparison of Experimental with Calculative Approaches
- 1 January 1990
- journal article
- research article
- Published by Wiley in Quantitative Structure-Activity Relationships
- Vol. 9 (1) , 21-28
- https://doi.org/10.1002/qsar.19900090105
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Corneal Penetration Behavior of β-Blocking Agents I: Physicochemical FactorsJournal of Pharmaceutical Sciences, 1983
- High performance liquid chromatographic capacity factor and partition coefficient relationship in a benzamide seriesInternational Journal of Pharmaceutics, 1981
- An investigation of the comparative liposolubilities of β-adrenoceptor blocking agentsJournal of Pharmacy and Pharmacology, 1981
- The clinical importance of cardioselectivity and lipophilicity in beta blockersAmerican Heart Journal, 1980
- Effects of different buffer species on partition coefficients of drugs used in quantitative structure–activity relationshipsJournal of Pharmaceutical Sciences, 1980
- Calculation of hydrophobic constant (log P) from .pi. and f constantsJournal of Medicinal Chemistry, 1975
- .beta.-Adrenoceptor studies. 1. In vitro .beta.-adrenergic blocking, antiarrhythmic, and local anesthetic activities of a new series of aromatic bis(2-hydroxy-3-isopropylaminopropyl) ethersJournal of Medicinal Chemistry, 1974
- Local anesthetic activity of 2-piperazinecarboxanilidesJournal of Medicinal Chemistry, 1972
- Die Eiwei bindung einiger Psychopharmaka mit tricyclischem Ringsystem in Abh ngigkeit von ihrer chemischen KonstitutionNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1970
- A New Substituent Constant, π, Derived from Partition CoefficientsJournal of the American Chemical Society, 1964