Design, synthesis, and structure–activity relationships of indole-3-heterocycles as agonists of the CB1 receptor
作者:Angus J. Morrison、Julia M. Adam、James A. Baker、Robert A. Campbell、John K. Clark、Jean E. Cottney、Maureen Deehan、Anna-Marie Easson、Ruth Fields、Stuart Francis、Fiona Jeremiah、Neil Keddie、Takao Kiyoi、Duncan R. McArthur、Karsten Meyer、Paul D. Ratcliffe、Jurgen Schulz、Grant Wishart、Kazuya Yoshiizumi
DOI:10.1016/j.bmcl.2010.10.093
日期:2011.1
Novel indole-3-heterocycles were designed and synthesized and found to be potent CB1 receptor agonists. Starting from a microsomally unstable lead , a bioisostere approach replacing a piperazine amide was undertaken. This was found to be a good strategy for improving stability both in vitro and in vivo. This led to the discovery of , which had an increased duration of action in the mouse tail flick
设计并合成了新型吲哚-3-杂环化合物,并发现其是有效的 CB1 受体激动剂。从微粒体不稳定的铅开始,采用生物等排体方法替代哌嗪酰胺。这被发现是提高体外和体内稳定性的良好策略。结果发现,与先导物相比,它在小鼠甩尾测试中的作用持续时间更长。