Synthesis and functional characterization of novel derivatives related to oxotremorine and oxotremorine-M

被引:42
作者
Dallanoce, C
Conti, P
De Amici, M
De Micheli, C
Barocelli, E
Chiavarini, M
Ballabeni, V
Bertoni, S
Impicciatore, M
机构
[1] Univ Studi Milano, Ist Chim Farmaceut & Tossicol, I-20131 Milan, Italy
[2] Univ Studi Parma, Ist Farmacol & Farmacognosia, I-43100 Parma, Italy
关键词
synthesis; oxotremorine; oxotremorine-M; muscarinic agonists; vas deferens; left atrium; ileum; tremorigenic activity;
D O I
10.1016/S0968-0896(99)00107-8
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
Two subseries of nonquaternized (5a-10a) and quaternized derivatives (5b-10b) related to oxotremorine and oxotremorine-M were synthesized and tested. The agonist potency at the muscarinic receptor subtypes of the new compounds was estimated in three classical in vitro functional assays: M-1 rabbit vas deferens, M-2 guinea pig left atrium and M-3 guinea pig ileum. In addition, the occurrence of central muscarinic effects was evaluated as tremorigenic activity after intraperitoneal administration in mice. In in vitro tests a nonselective muscarinic activity was exhibited by all the derivatives with potencies values that, in some instances, surpassed those of the reference compounds (i.e. 8b). Functional selectivity was evidenced only for the oxotremorine-like derivative 9a, which behaved as a mixed M-3-agonist/M-1-antagonist (pD(2)-5.85; pA(2)=4.76, respectively). In in vivo tests nonquaternary compounds were able to evoke central muscarinic effects, with a potency order parallel to that observed in vitro. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1539 / 1547
页数:9
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