Solid-phase synthesis and pharmacological evaluation of analogues of PhTX-12 - A potent and selective nicotinic acetylcholine receptor antagonist

被引:22
作者
Stromgaard, K
Mellor, IR
Andersen, K
Neagoe, I
Pluteanu, F
Usherwood, PNR
Krogsgaard-Larsen, P
Jaroszewski, JW
机构
[1] Royal Danish Sch Pharm, Dept Med Chem, DK-2100 Copenhagen, Denmark
[2] Royal Danish Sch Pharm, NeuroSci PharmaBiotec Res Ctr, DK-2100 Copenhagen, Denmark
[3] Univ Nottingham, Sch Life & Environm Sci, Div Mol Toxicol, Nottingham NG7 2RD, England
[4] H Lundbeck & Co AS, Dept Combinatorial Chem, DK-2500 Copenhagen, Denmark
关键词
D O I
10.1016/S0960-894X(02)00120-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Philanthotoxin-12 (PhTX-12) is a novel potent and selective, noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs). Homologues of PhTX-12 with 7-11 methylene groups between the primary amino group and the aromatic head-group were synthesized using solid-phase methodology. In vitro electrophysiological studies of nAChR demonstrated that decreasing the number of methylene groups from 12 to 11 significantly increased potency. Antagonism by PhTX-11, like that of PhTX-12 was only weakly voltage-dependent. When the methylene spacer was reduced further, antagonism vas decreased below that of PhTX-12, and in some cases potentiation of ACh responses by up to 60% was observed. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1159 / 1162
页数:4
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