Pyrrolo[1,2-b]pyridazines, pyrrolo[2,1-f]triazin-4(3H)-ones, and related compounds as novel corticotropin-releasing factor 1 (CRF1) receptor antagonists

被引:15
|
作者
Saito, Tetsuji [1 ]
Obitsu, Tetsuo [1 ]
Kohno, Hiroshi [1 ]
Sugimoto, Isamu [1 ]
Matsushita, Takeshi [1 ]
Nishiyama, Taihei [1 ]
Hirota, Tomoko [1 ]
Takeda, Hiroyuki [1 ]
Matsumura, Naoya [1 ]
Ueno, Sonoko [1 ]
Kishi, Akihiro [1 ]
Kagamiishi, Yoshifumi [1 ]
Nakai, Hisao [1 ]
Takaoka, Yoshikazu [1 ]
机构
[1] Ono Pharmaceut Co Ltd, Minase Res Inst, Mishima, Osaka 6188585, Japan
关键词
Corticotropin-releasing factor 1 receptor; Antagonist; MAJOR DEPRESSION; HORMONE; ANXIETY; DMP696; DERIVATIVES; R121919; SYSTEM;
D O I
10.1016/j.bmc.2011.11.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To identify structurally novel corticotropin-releasing factor 1 (CRF1) receptor antagonists, a series of bicyclic core analogs pyrrolo[1,2-b]pyridazines and pyrrolo[2,1-f]triazin-4(3H)-ones, which were designed based on a monocyclic core antagonist, was synthesized and evaluated. Among the compounds tested, 2-difluoromethoxy-4-methylpyridin-5-yl analog 27 was found to show efficacy in a dose-dependent manner in an elevated plus maze test in rats. The discovery process and structure-activity relationship is presented. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1122 / 1138
页数:17
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