Zobrazeno 1 - 7
of 7
pro vyhledávání: '"W L Kurtz"'
Autor:
G P Dubé, Mais De, W L Kurtz, Joseph A. Jakubowski, K A Brune, Barbara G. Utterback, F. Mohamadi, M. M. Spees
Publikováno v:
ChemInform. 23
A number of phenylsulfonamido derivatives have been synthesized and tested for their ability to inhibit: a) thromboxane A 2 /prostaglandin H 2 ( TXA 2 PGH 2 ) mimetic (U46619)- induced guinea pig platelet aggregation; b) aortic ring contraction; and
Autor:
G P Dubé, Joseph A. Jakubowski, M. M. Spees, K A Brune, W L Kurtz, Mais De, F. Mohamadi, Barbara G. Utterback
Publikováno v:
European Journal of Medicinal Chemistry. 26:821-827
A number of phenylsulfonamido derivatives have been synthesized and tested for their ability to inhibit: a) thromboxane A 2 /prostaglandin H 2 ( TXA 2 PGH 2 ) mimetic (U46619)- induced guinea pig platelet aggregation; b) aortic ring contraction; and
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 272(2)
A novel thromboxane A2/prostaglandin H2 (TXA2/PGH2) receptor ligand, (+)5(Z)-7-[3-endo-phenylsulfonylamino[2.2.1]-bicyclohept-2-e xo- yl]-heptenoic acid [(+)-S-145], was evaluated in guinea pigs to assess the in vivo pharmacodynamic profile of this c
Autor:
G P, Dubé, D E, Mais, J A, Jakubowski, K A, Brune, B G, Utterback, T A, True, L E, Rinkema, W L, Kurtz
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 262(2)
The stereoisomers of S-145, a novel thromboxane A2/prostaglandin H2 (TXA2/PGH2) receptor ligand, were compared to TXA2/PGH2 receptor antagonists, SQ29548 and BM13505 in guinea pig platelets, aortas and trachea. Equilibrium binding assays in platelets
Publikováno v:
Molecular pharmacology. 39(1)
Thromboxane A2 (TXA2) and prostaglandin H2 (PGH2) are potent constrictors of airway smooth muscle and may mediate some of the pulmonary effects of leukotrienes. To date, the TXA2/PGH2 receptor in lung has not been well characterized. In this report,
Publikováno v:
Japanese Journal of Pharmacology. 75:54
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 199(2)
Oral administration of l-propoxyphene with d-propoxyphene enhances the analgesic activity of d-propoxyphene as expressed in the rat tail heat test. The combination of d- and l-propoxyphene at a dose of 10 mg/kg each was found to have activity in the