Kubo K, Nakamura J, Karasawa A, Shuto K, Nakamizo N
Arzneimittelforschung. 1983;33(7):926-31.
4-(2-Hydroxy-3-[(1-methyl-3-phenylpropyl)amino] propoxy)benzeneacetamide (KF-4317) differs from conventional adrenoceptor antagonists in producing a competitive blockade at both alpha- and beta 1-adrenoceptors. In blocking beta 1-adrenoceptors, KF-4317 is as active as labetalol in both in vitro and in vivo experiments, and 22 times less potent (in vitro) and 2 times less potent (in vivo) than propranolol. In blocking beta 2-adrenoceptors, KF-4317 is 776 times less potent (in vitro) and 83 times less potent (in vivo) than propranolol. The ratio of beta 1-blocking activity to beta 2-blocking activity is 33 to 145 for practolol, 37 for KF-4317, 1 for propranolol and 0.16 to 1 for labetalol, respectively. In blocking alpha-adrenoceptors, KF-4317 is 55 times less potent than phentolamine and 6 times less potent than labetalol in in vitro experiments, but as active as labetalol in in vivo experiments. These results show that KF-4317 possesses a novel type of adrenoceptor antagonistic property.
4-(2-羟基-3-[(1-甲基-3-苯基丙基)氨基]丙氧基)苯乙酰胺(KF-4317)与传统的肾上腺素能受体拮抗剂不同,它对α和β1肾上腺素能受体均产生竞争性阻断作用。在阻断β1肾上腺素能受体方面,KF-4317在体外和体内实验中的活性与拉贝洛尔相当,其效力(体外)比普萘洛尔低22倍,(体内)低2倍。在阻断β2肾上腺素能受体方面,KF-4317的效力(体外)比普萘洛尔低776倍,(体内)低83倍。醋丁洛尔的β1阻断活性与β2阻断活性之比为33比145,KF-4317为37,普萘洛尔为1,拉贝洛尔为0.16比1。在阻断α肾上腺素能受体方面,在体外实验中KF-4317的效力比酚妥拉明低55倍,比拉贝洛尔低6倍,但在体内实验中其活性与拉贝洛尔相当。这些结果表明KF-4317具有一种新型的肾上腺素能受体拮抗特性。