Synthesis and pharmacological evaluation of carbamic acid 1-phenyl-3-(4-phenyl-piperazine-1-yl)-propyl ester derivatives as new analgesic agents

被引:20
作者
Chae, Eunhee [1 ]
Yi, Hanju [1 ]
Choi, Yeonjung [1 ]
Cho, Hyeon [1 ]
Lee, Kiho [1 ]
Moon, Hongsik [1 ]
机构
[1] SK Biopharmaceut, Div Life Sci, Taejon 305712, South Korea
关键词
Arylpiperazine; Analgesic; Anti-nociceptive; 5-HT2A antagonism; 5-HT1A; RATS;
D O I
10.1016/j.bmcl.2012.02.023
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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-HT2A 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. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2434 / 2439
页数:6
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