Neuronal nAChR stereoselectivity to non-natural epibatidine derivatives

被引:15
作者
Bertrand, S
Patt, JT
Spang, JE
Westera, G
Schubiger, PA
Bertrand, D
机构
[1] Ctr Med Univ Geneva, Dept Physiol, Fac Med, CH-1211 Geneva 4, Switzerland
[2] Swiss Fed Inst Technol, Ctr Radiopharmaceut Sci, Zurich, Switzerland
[3] Paul Scherrer Inst, Villigen, Switzerland
[4] Univ Zurich Hosp, Dept Radiol, Clin Nucl Med, CH-8091 Zurich, Switzerland
来源
FEBS LETTERS | 1999年 / 450卷 / 03期
关键词
nicotinic acetylcholine receptor; brain; epibatidine; pharmacophore; imaging;
D O I
10.1016/S0014-5793(99)00473-1
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
The frog toxin epibatidine is one of the most powerful ligands of the neuronal nicotinic receptors and derivatives show promising possibilities for labeling in positron emission tomography studies. In an attempt to reduce epibatidine toxicity, new methyl derivatives were synthesized, tested in positron emission tomography imaging and in electrophysiology. labeling as well as physiological experiments highlighted the differences in sensitivity of the neuronal nicotinic acetylcholine receptors between two methyl enantiomers and the reduction in sensitivity caused by introducing the methyl group, At present, epibatidine derivatives seem the most promising compounds for in vivo labeling of neuronal nicotinic acetylcholine receptors, (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:273 / 279
页数:7
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