1984 年 104 巻 1 号 p. 28-36
Twenty one kinds of 8-acylamino-5-(2-hydroxy-3-substituted aminopropoxy)-3, 4-dihydrocarbostyril derivatives were synthesized and their antagonistic activities on isoproterenol were examined. Several compounds having 3, 4-dimethoxyphenethyl or 4-carbamoylphenoxyethyl moiety in 3-substituted amino group were found to have less antagonistic activity on isoproterenol than those with tert-butyl or isopropyl moiety in 3-substituted amino group, but showed relative higher selectivity for β1-adrenoreceptors in the anesthetized dog.