Zobrazeno 1 - 10
of 62
pro vyhledávání: '"H, Ramuz"'
Publikováno v:
Journal of Mass Spectrometry, Vol. 31, No 1 (1996) pp. 69-76
For metabolic studies the fragmentation of a novel endothelin receptor antagonist, Bosentan, was investigated using ionspray tandem mass spectrometry. Bosentan belongs to the sulphonamide class and a complicated and unexpected fragmentation at low en
Autor:
Ikuo Horii, C. Konishi, K. Kobayashi, J.F. Eliason, R. Sawada, Shigeyasu Ichihara, Isami Kuruma, T. Tsukaguchi, H. Ramuz
Publikováno v:
European Journal of Cancer. 31:2354-2361
The multidrug resistance modifying activity of a dithiane analogue of tiapamil, Ro 44-5912, was examined in vivo . Results of acute toxicity studies in mice indicated that lethal toxicity occurred with doses greater than 1 mmol/kg of body weight. In
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 290(2)
Tezosentan (Ro 61-0612) [5-isopropyl-pyridine-2-sulfonic acid 6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-2-(2-1H-tetrazol-5-yl-+ ++pyri din-4-yl)-pyrimidin-4-ylamide] is a new endothelin (ET) receptor antagonist specifically designed for parenteral u
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 283(3)
Endothelin (ET) receptor antagonists are of great potential clinical interest for the treatment pathological conditions associated with vasospasm, such as subarachnoid hemorrhage (SAH). We developed for parenteral use a compound of a class of trifunc
Publikováno v:
Helvetica Chimica Acta. 45:789-805
L'etude du systeme ternaire K+NH4+NO3H2O a 25° a conduit a un diagramme de solubilite compose de 4 courbes representant les solutions saturees des phases solides suivantes: cristaux mixtes du type KNO3 (symbole K0), contenant de 0 a 13,3 eq.-% NH4+,
Publikováno v:
The Journal of Pharmacology and Experimental Therapeutics; December 1997, Vol. 283 Issue: 3 p1110-8, 9p
Publikováno v:
Chemischer Informationsdienst. 11
Publikováno v:
Chemischer Informationsdienst. 13
Autor:
H, Ramuz
Publikováno v:
Arzneimittel-Forschung. 28(11)
The alkylation of 2-(3,4-dimethoxyphenyl)-m-dithiane-1,1,3,3-tetraoxide (4) with N-(3-chloropropyl)-3,4-dimethoxy-N-methylphenethylamine (2) leads to N-(3,4-dimethoxyphenethyl)-2-(3,4-dimethoxyphenyl)-N-methyl-m-dithiane-2-propylamine-1,1,3,3-tetraox
Autor:
H, Ramuz
Publikováno v:
Helvetica chimica acta. 58(7)