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Sila-difenidol

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

In vitro tests with the pair 173ajl 73b on the left auricle of guinea pigs resulted also in different intensities of activity. Both compounds were found to lead to a prolongation of the refractory period. However, sila-difenidol exhibits a significant... [Pg.60]

Based on the cyclic-blocking moieties and other substituent groups, subtype-selective muscarinic antagonists can be classified into eight groups (l)tricyclic benzodiazepines, (2) benzothiazepines, (3) quinuclidines, (4) poly-methylene tetramines, (5)indenes, ( 6)sila-difenidols, (7) diphenylacetyloxy derivatives, and (.8) himbacine akaloids. [Pg.128]

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]

See other pages where Sila-difenidol is mentioned: [Pg.196]    [Pg.211]    [Pg.56]    [Pg.59]    [Pg.59]    [Pg.60]    [Pg.2364]    [Pg.109]    [Pg.132]    [Pg.52]    [Pg.52]    [Pg.58]    [Pg.278]    [Pg.1177]    [Pg.2364]   
See also in sourсe #XX -- [ Pg.2364 ]

See also in sourсe #XX -- [ Pg.2364 ]



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Difenidol

Hexahydro-sila-difenidol

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