Life Science Division, SK Biopharmaceuticals, Daejeon 305-712, Republic of Korea.
Bioorg Med Chem Lett. 2012 Apr 1;22(7):2434-9. doi: 10.1016/j.bmcl.2012.02.023. Epub 2012 Feb 16.
A series of carbamic acid 1-phenyl-3-(4-phenyl-piperazine-1-yl)-propyl ester derivatives were synthesized through discovery strategies for balancing target-based in vitro screening and phenotypic in vivo screening. All the newly synthesized compounds were screened for their analgesic activities and compared with standard drug morphine. Among them, compound 44r, a potent analgesic agent that has favorable pharmacokinetic properties in rats and most importantly, has a wide safety margin. We demonstrated with in vitro and in vivo functional assays that its analgesic activity might be through 5-HT(2A) antagonism to some extent. Hence, it is concluded that there is ample scope for further study in developing compound 44r as a good lead candidate for an analgesic agent.
通过平衡基于靶标的体外筛选和表型体内筛选的发现策略,合成了一系列氨基甲酸 1-苯基-3-(4-苯基-哌嗪-1-基)-丙酯衍生物。所有新合成的化合物均进行了镇痛活性筛选,并与标准药物吗啡进行了比较。其中,化合物 44r 是一种有效的镇痛剂,在大鼠中具有良好的药代动力学特性,最重要的是具有较宽的安全范围。我们通过体外和体内功能测定证明,其镇痛活性可能在一定程度上通过 5-HT(2A)拮抗作用实现。因此,可以得出结论,进一步研究开发化合物 44r 作为一种良好的镇痛剂先导候选物具有很大的空间。