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Publikováno v:
Collection of Czechoslovak Chemical Communications. 67:336-352
Two ways are shown to transform cardioactive cardenolides into cardenamides [17β-(5-oxo-2,5-dihydropyrrol-3-yl)-5β,14β-androstane derivatives], and their derivatives by replacement of their ring oxygen by N-R. Cardioactivity is strongly decreased
Autor:
Rudolf Megges, Rudolf Schön, Kurt R. H. Repke, Horst Büchting, Bernd Undeutsch, Jürgen Weiland
Publikováno v:
Steroids. 63:464-469
To improve the weak inhibitory effect of 3-oxo-17 alpha-pregna-4,6-diene-21,17-carbolactone (canrenone, II) on Na+/K(+)-ATPase activity in human heart muscle, we have investigated the impact of hydrogenation, reduction, glycosidation, and the introdu
Publikováno v:
Journal of Enzyme Inhibition. 12:53-58
Publikováno v:
Angewandte Chemie International Edition in English. 34:282-294
“The following remarks consist partially of matter of fact, and partially of opinion. The former will be permanent; the latter must vary with the detection of error, or the improvement of knowledge. I hazard them with diffidence, and hope they will
Publikováno v:
Angewandte Chemie. 107:308-321
Der Arzt William Withering fuhrte 1785 mit seinem Buch „An Account of the Foxglove and some of its Medical Uses” Praparate aus Digitalisblattern in die Therapie der Wassersucht (des Herzversagens) ein und erklarte: „The following remarks consis
Publikováno v:
European Journal of Medicinal Chemistry. 30:763-767
Summary Acetates of gomphogenin and gomphoside have been synthesized and their structures established by NMR measurements, optical rotation, mass and infrared spectrometry. The kinetic and equilibrium parameters of the inhibitory interaction of the c
Autor:
Kurt R. H. Repke, Rudolf Schön
Publikováno v:
Biological Reviews. 69:119-145
The original aim of the review has been to probe into the validity of the paradigm on the high energy-carrier function of ATP. It seemed to be called into question on the basis of findings with H(+)-transporting ATP synthase suggesting the formation
Publikováno v:
Journal of Enzyme Inhibition. 8:197-205
The glycosidic moiety plays an important role in the pharmacokinetic and pharmacodynamic behaviour of cardiac glycosides like digitoxin and digoxin. Their tridigitoxoside side chain becomes slowly removed in the animal body and hence delays the inact