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J Med Chem ; 26(7): 950-7, 1983 Jul.
Article in English | MEDLINE | ID: mdl-6134834

ABSTRACT

A series of 2-[4-[3-(substituted-amino)-2-hydroxypropoxy]phenyl]imidazoles is described. The compounds were investigated in vitro for beta-adrenoceptor antagonism, and several examples were found to be selective for the beta 1-adrenoceptor. The structure--activity relationship exhibited by this series of compounds is discussed. (S)-2-[p-[3-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-2-hydroxypropoxy]phenyl]-4-(2 -thienyl)imidazole [(S)-13] was over 100 times more selective than atenolol for the beta 1-adrenergic receptor and has been selected for in-depth studies.


Subject(s)
Adrenergic alpha-Agonists/chemical synthesis , Imidazoles/chemical synthesis , Receptors, Adrenergic, beta/chemical synthesis , Receptors, Adrenergic/chemical synthesis , Animals , Female , Guinea Pigs , Heart/drug effects , Heart/physiology , Imidazoles/pharmacology , Indicators and Reagents , Isoproterenol/pharmacology , Magnetic Resonance Spectroscopy , Receptors, Adrenergic, beta/pharmacology , Structure-Activity Relationship
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