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Hexahydro-difenidol

Lambrecht, G., Feifel, R., Moser, U., Wagner-Rdder, M., Choo, L.K., Camus, J., Tastenoy, M., Waelbroeck, M., Strohmann, C., Tacke, R., Rodrigues de Miranda, J.F., Christophe, J., Mutschler, E., 1989. Pharmacology of hexahydro-difenidol, hexahydro-sila-difenidol and related selective muscarinic antagonists. TIPS, Suppl. 60-64. [Pg.65]

Mutschler, E. Affinity profiles of hexahydro-sila-difenidol analogues at muscarinic receptor subtypes. [Pg.155]

Fig. 3. Activation of Icat requires M2 receptor binding and an increase in [Ca Jj. The Ms receptor antagonist hexahydro-sil-difenidol (0.4 M) completely inhibits the response to methacholine (50 M). However, if caffeine (8 mM) is used to release... Fig. 3. Activation of Icat requires M2 receptor binding and an increase in [Ca Jj. The Ms receptor antagonist hexahydro-sil-difenidol (0.4 M) completely inhibits the response to methacholine (50 M). However, if caffeine (8 mM) is used to release...

See other pages where Hexahydro-difenidol is mentioned: [Pg.52]    [Pg.1176]    [Pg.52]    [Pg.1176]    [Pg.2364]    [Pg.52]    [Pg.58]    [Pg.1177]    [Pg.161]    [Pg.2364]   
See also in sourсe #XX -- [ Pg.52 , Pg.58 ]




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Hexahydro-sila-difenidol

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