Predicting Dyspnea Inducers by Molecular Topology
QSAR based on molecular topology (MT) is an excellent methodology used in predicting physicochemical and biological properties of compounds. This approach is applied here for the development of a mathematical model capable to recognize drugs showing dyspnea as a side effect.
María Gálvez-Llompart +4 more
wiley +1 more source
Novel high/low solubility classification methods for new molecular entities. [PDF]
Dave RA, Morris ME.
europepmc +1 more source
A quantitative threshold for high/low extent of urinary excretion of compounds in humans. [PDF]
Dave RA, Morris ME.
europepmc +1 more source
Procainamide, but not N-acetylprocainamide, induces protein free radical formation on myeloperoxidase: a potential mechanism of agranulocytosis. [PDF]
Siraki AG +6 more
europepmc +1 more source
ABC of monitoring drug therapy. Measuring plasma drug concentrations. [PDF]
Aronson JK, Hardman M.
europepmc +1 more source
Are there environmental forms of systemic autoimmune diseases? [PDF]
Hess EV.
europepmc +1 more source
Metabolites of procainamide and practolol inhibit complement components C3 and C4. [PDF]
Sim E, Stanley L, Gill EW, Jones A.
europepmc +1 more source
BDDCS applied to over 900 drugs. [PDF]
Benet LZ, Broccatelli F, Oprea TI.
europepmc +1 more source
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Analysis of procainamide hydrochloride and acecainide hydrochloride in rat feed
Journal of Pharmaceutical Sciences, 1980An extraction and GLC assay procedure was developed for quantitation of procainamide hydrochloride and acecainide hydrochloride in rat feed. 4-Amino-N-[2-(dipropylamino)ethyl]benzamide hydrochloride was synthesized and utilized as an internal standard.
J E, Carter +5 more
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Acecainide pharmacokinetics in normal subjects of known acetylator phenotype
Biopharmaceutics & Drug Disposition, 1991AbstractThe purpose of this study was to determine the pharmacokinetics of acecainide (formerly N‐acetylprocainamide) in six normal subjects of known acetylator phenotype. Three subjects were fast acetylators and three slow acetylators by sulfapyridine phenotyping criteria.
J D, Coyle, H, Boudoulas, J J, Lima
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