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pro vyhledávání: '"F.W. Schueler"'
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Autor:
G. Alan Robison, F.W. Schueler
Publikováno v:
Journal of Pharmaceutical Sciences. 50:602-605
Several members of a new series of azlactone derivatives (substituted acrylic acid amides), which by themselves exhibit convulsant properties, were found to be capable of prolonging the duration of hexobarbital-induced hypnosis in mice. Experiments a
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 38:74-81
The relation between chemical constitution and analgetic action has been investigated in several compound types which bear a Structural relationship to the morphine-type analgetics. Analgetic potency has been demonstrated in several compound types.
Autor:
F.W. Schueler, Floyd R. Domer
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 49:553-556
Synthesis of C I4 -labeled hemicholinium No. 3 (HC-3) with a specific activity of 2.788 mc./m M is described. Twenty-four hour studies of rats in metabolism cages indicated 57.5 per cent of an injected dose is excreted in the urine, 15.6 per cent is
Autor:
H. H. Keasling, F.W. Schueler
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 45:792-796
A group of polymeric quaternary ammonium salts have been synthesized and studied pharmacologically. The polymers exhibited a high degree of neuromuscular blocking potency. The results have been discussed both in regard to their theoretic and practica
Autor:
F.W. Schueler, H. H. Keasling
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 43:98-101
Details concerning the synthesis and pharmacologic evaluation of a new hexamethonium ganglionic blocking agent containing a "built-in" muscarinic moiety are described. The inclusion of this latter moiety may be regarded as an attempt to increase para
Autor:
F.W. Schueler, John P. Long
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 43:79-86
In a series of bis onium biphepyl derivatives, alteration of substitutions on the quaternary nitrogen produced a wide variation in toxicity and ability to inhibit cholinesterase, as well as other pharmacological responses. Three members of this serie
Publikováno v:
Journal of Pharmaceutical Sciences. 55:381-386
Norphenyl HC-3 (NP-HC-3), an analog of HC-3 in which the biphenyl nucleus is replaced by a monophenyl moiety, has been synthesized. NP-HC-3 has been shown to resemble the parent compound in most of its pharmacological properties. Its LD50 in mice was
Autor:
H. H. Keasling, F.W. Schueler
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 39:87-90
The relation between chemical constitution and estrogenic action has been investigated in a group of azomethine derivatives comprising all 4,4′ substitution combinations of four groups—H, CH3, CH3O, OH. 4,4′-Dihydroxy benzylidene aniline produc
Autor:
F.W. Schueler
Publikováno v:
Journal of the American Dietetic Association. 29:1118-1123