Gao Feng-Li, Wang Xin, Zhang Hong-Mei, Cheng Tie-Ming, Li Run-Tao
School of Pharmaceutical Sciences, Peking University, Beijing 100083, PR China.
Bioorg Med Chem Lett. 2003 May 5;13(9):1535-7. doi: 10.1016/s0960-894x(03)00177-x.
Based on the structure of compound 3, two series of spirocyclopiperazinium derivatives 7a-n and 10a-h were synthesized and evaluated for their in vivo analgesic and sedative activities. Compounds 7f and 10c were discovered to exhibit excellent analgesic activity. Structure-activity relationships revealed that anion of the quaternary salt affected the analgesic and sedative activity significantly; the allyl group is a most effective group among the compounds 7a-n; the electron-released substitute on the aromatic ring is favorable to increase the analgesic activity.
基于化合物3的结构,合成了两个系列的螺环哌嗪鎓衍生物7a - n和10a - h,并对其体内镇痛和镇静活性进行了评价。发现化合物7f和10c具有优异的镇痛活性。构效关系表明,季铵盐的阴离子对镇痛和镇静活性有显著影响;烯丙基是化合物7a - n中最有效的基团;芳环上的供电子取代基有利于提高镇痛活性。