作者:Yossef Itzhak、Asher Kalir、Ben Avi Weissman、Sasson Cohen
DOI:10.1021/jm00137a004
日期:1981.5
1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol (10) and its propionate (11), and 1-(1-phenylcyclohexyl)-4-phenylpiperidine (13) were prepared and characterized. The new compounds, which are derived from phencyclidine, exerted analgesic activity in mice. The most potent is 10, which is twice as active as morphine. The antinociceptive activity of 10, 11, and 13 could be well correlated with their potency in the mouse
1-(1-苯基环己基)-4-哌啶醇(3),1-(1-苯基环己基)-4-苯基-4-哌啶醇(10)及其丙酸酯(11)和1-(1-苯基环己基)的几种酯制备并表征了)-4-苯基哌啶(13)。衍生自苯环利定的新化合物在小鼠中发挥镇痛作用。最有效的是10,活性是吗啡的两倍。10、11和13的抗伤害感受活性可能与它们在小鼠输精管生物测定中的功效密切相关,并且纳洛酮可完全逆转两者。