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Gallamine

Gallamine triethiodide Ibuprofen Nalidixic acid Oxetorone fumarate Oxolinic acid Piroheptine Rosoxacin Tridihexethyl iodide Ethyl 4-iodobutyrate Meptazinol... [Pg.1634]

Kenakin, T. P., and Boselli, C. (1989). Pharmacologic discrimination between receptor heterogeneity and allosteric interaction Resultant analysis of gallamine and pirenzeipine antagonism of muscarinic responses in rat trachea. J. Pharmacol. Exp. Ther. 250 944—952. [Pg.126]

C2H5I 75-03-6) see Butibufen Cinoxacin Diethylstilbestrol Enoxacin Ethotoin Gallamine triethiodide Imiquimod Lomefloxacin Mosapride citrate Nalidixic acid Oxolinic acid Pefloxacin Pipemidic acid Tridihexethyl chloride Zaleplon... [Pg.2381]

Clark AL, Mitchelson F. The inhibitory effect of gallamine on muscarinic receptors. Br J Pharmacol 1976 58 323-331. [Pg.246]

Stockton JM, Birdsall NJ, Burgen AS, Hulme EC. Modification of the binding properties of muscarinic receptors by gallamine. Mol Pharmacol 1983 23 551-557. [Pg.246]

Ehlert FJ. Gallamine allosterically antagonizes muscarinic receptor-mediated inhibition of adenylate cyclase activity in the rat myocardium. J Pharmacol Exp Ther 1988 247 596-602. [Pg.246]

Dunlap J, Brown JH. Heterogeneity of binding sites on cardiac muscarinic receptors induced by the neuromuscular blocking agents gallamine and pancuronium. Mol Pharmacol 1983 24 15-22. [Pg.246]

Waelbroeck M, Robberecht P, De Neef P, Christphe J. Effects of d-tubocurarine on rat cardiac muscarinic receptors a comparison with gallamine. J Recept Res 1988 8 787-808. [Pg.246]

Vecuronium Rocuronium Pancuronium Atracurium Cis-atracurium Mivacurium Gallamine Tubocurare... [Pg.228]

IC50 curves were also recorded for various other inhibitors and the corresponding IC50 values were calculated. The determined IC50 values of 9-aminoacridine, galanthamine, gallamine, (—)-Huperzine A and thioflavin T were 0.12 pM, 0.38 pM, 6.4 pM, 0.46 pM, and 3.2 pM, respectively. It was difficult to compare these values with comparable values in literature since often different types of AChE, or AChE isolated from different organisms were used and different assay conditions were applied. However, the relative activities of the used inhibitors compared well with those reported in literature, except for (—)-huperzine A, which was found to be relatively less active then was expected. [Pg.197]

See other pages where Gallamine is mentioned: [Pg.431]    [Pg.271]    [Pg.168]    [Pg.717]    [Pg.1628]    [Pg.1700]    [Pg.1736]    [Pg.128]    [Pg.135]    [Pg.136]    [Pg.145]    [Pg.268]    [Pg.270]    [Pg.270]    [Pg.270]    [Pg.271]    [Pg.798]    [Pg.950]    [Pg.950]    [Pg.950]    [Pg.2350]    [Pg.2439]    [Pg.2452]    [Pg.129]    [Pg.227]    [Pg.231]    [Pg.231]    [Pg.64]    [Pg.172]    [Pg.187]    [Pg.197]    [Pg.114]    [Pg.1119]    [Pg.12]    [Pg.13]    [Pg.13]   
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Gallamine triethiodide

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