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CB1大麻素受体拮抗剂的最新进展。

Recent advances in CB1 cannabinoid receptor antagonists.

作者信息

Lange Jos H M, Kruse Chris G

机构信息

Solvay Pharmaceuticals, Research Laboratories, CJ van Houtenlaan 36, 1381 CP, Weesp, the Netherlands.

出版信息

Curr Opin Drug Discov Devel. 2004 Jul;7(4):498-506.

Abstract

Cannabinoid CB1 receptor antagonists are currently the subject of intensive research due to their highly promising therapeutic prospects. Novel chemical entities having CB1 antagonistic properties have recently been disclosed by several pharmaceutical companies and some academic research groups, some of which are close structural analogs of the leading compound rimonabant (SR-141716A; Sanofi-Synthélabo). A considerable number of these CB1 antagonists are bioisosteres that are derived from rimonabant by the replacement of the pyrazole moiety with an alternative heterocycle. As well as these achiral compounds, Solvay Pharmaceuticals have disclosed a novel class of chiral pyrazolines that are potent and CB1/CB2 subtype-selective cannabinoid receptor antagonists, in which the interactions with the CB1 receptor are highly stereoselective.

摘要

由于大麻素CB1受体拮抗剂具有极具前景的治疗前景,目前正处于深入研究阶段。几家制药公司和一些学术研究小组最近公布了具有CB1拮抗特性的新型化学实体,其中一些是先导化合物利莫那班(SR-141716A;赛诺菲-圣德拉堡)的紧密结构类似物。这些CB1拮抗剂中有相当一部分是生物电子等排体,它们是通过用另一种杂环取代吡唑部分而从利莫那班衍生而来的。除了这些非手性化合物外,索尔维制药公司还公布了一类新型的手性吡唑啉,它们是强效且CB1/CB2亚型选择性大麻素受体拮抗剂,其中与CB1受体的相互作用具有高度立体选择性。

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