Discovery of indole alkaloids with cannabinoid CB1 receptor antagonistic activity

被引:24
|
作者
Kitajima, Mariko [1 ]
Iwai, Masumi [1 ]
Kikura-Hanajiri, Ruri [2 ]
Goda, Yukihiro [2 ]
Iida, Mitsuru [3 ]
Yabushita, Hisatoshi [3 ]
Takayama, Hiromitsu [1 ]
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan
[2] Natl Inst Hlth Sci, Setagaya Ku, Tokyo 1588501, Japan
[3] Otsuka Pharmaceut Co Ltd, Kawaguchi, Tokushima 7710182, Japan
关键词
Cannabinoid; CB1; receptor; Antagonist; Indole alkaloid; Iboga; Voacanga; THERAPEUTIC APPLICATIONS; TABERNAEMONTANA;
D O I
10.1016/j.bmcl.2011.02.036
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Three indole alkaloids, voacamine (1), 3,6-oxidovoacangine (2), and a new alkaloid, 5-hydroxy-3,6-oxidovoacangine (3), isolated from Voacanga africana were found to exhibit potent cannabinoid CB1 receptor antagonistic activity. This is the first example of CB1 antagonists derived from natural alkaloids. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1962 / 1964
页数:3
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