Sun Qi, Yue Cai-Qin, Ye Jia, Li Chang-Ling, Cheng Tie-Ming, Li Run-Tao
School of Pharmaceutical Sciences, Peking University, Beijing 100083, PR China.
Bioorg Med Chem Lett. 2007 Nov 15;17(22):6245-9. doi: 10.1016/j.bmcl.2007.09.026. Epub 2007 Sep 8.
Two novel classes of monospirocyclopiperazinium salts were designed, synthesized, and evaluated for their in vivo analgesic activities. Some interesting structure-activity relationships are revealed: (1) Spirocyclopiperazinium moiety is favorable to improve the analgesic activity; (2) The size and conformation of spirocyclopiperazinium moiety significantly affects the analgesic activity; (3) Phenylethyl group of 3d is a crucial pharmacophore. Among the compounds synthesized, 3d exhibited the most potent activity with low toxicity. Further antinociceptive mechanism studies of 3d showed that these compounds will be a new kind of analgesics.
设计、合成了两类新型单螺环哌嗪鎓盐,并对其体内镇痛活性进行了评价。揭示了一些有趣的构效关系:(1)螺环哌嗪鎓部分有利于提高镇痛活性;(2)螺环哌嗪鎓部分的大小和构象显著影响镇痛活性;(3)3d的苯乙基是关键药效团。在合成的化合物中,3d表现出最强的活性且毒性低。对3d的进一步抗伤害感受机制研究表明,这些化合物将是一种新型镇痛药。