Synthesis, pharmacology and therapeutic potential of 10-methoxypyrazino[1,2-a]indoles, partial agonists at the 5HT(2C) receptor

被引:41
作者
Bos, M
Jenck, F
Martin, JR
Moreau, JL
Mutel, V
Sleight, AJ
Widmer, U
机构
[1] Pharma Division, Preclinical CNS Research, F. Hoffmann-La Roche Ltd.
关键词
pyrazinoindole; serotonin; 5HT(2C) receptor; partial agonist; psychiatric disorder;
D O I
10.1016/S0223-5234(97)83976-1
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of new 10-methoxypyrazino[1,2-a]indoles has been prepared and shown to be 5HT(2C) receptor ligands. The studied compounds 10a-j were found to act as partial agonists at the 5HT(2C) receptor, binding with high affinity and moderate selectivity versus 5HT(1A) and 5HT(2A) receptors, but inducing only a submaximal increase in phosphoinositol formation. Compound 10j was demonstrated to be active in animal models of obsessive-compulsive disorder, depression and panic anxiety.
引用
收藏
页码:253 / 261
页数:9
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