Bondavalli F, Bruno O, Ranise A, Schenone P, Filippelli A, Marrazzo R, Di Guglielmo R, Marmo E
Farmaco Sci. 1986 Aug;41(8):630-6.
The synthesis of a series of N-substituted 3-amino-2-hydroxypropyl ethers (III a-1) starting from (+)-1,3,3-trimethyl-2-oxabicyclo [2.2.2]-octan-6-hydroxyimine is described. Some of these compounds showed a remarkable hypotensive and a weak bradycardic activity in rats, as well as a moderate local anesthetic activity in mice. All compounds were found to be devoid of antiarrhythmic activity in rats and of beta-blocking activity in dogs.
描述了从(+)-1,3,3-三甲基-2-氧杂双环[2.2.2]辛烷-6-羟基肟开始合成一系列N-取代的3-氨基-2-羟丙基醚(III a-1)。其中一些化合物在大鼠中表现出显著的降压活性和微弱的心动过缓活性,在小鼠中还表现出中等程度的局部麻醉活性。所有化合物在大鼠中均无抗心律失常活性,在犬中无β受体阻断活性。