PARA-FLUORO-HEXAHYDRO-SILA-DIFENIDOL - THE 1ST M2-BETA-SELECTIVE MUSCARINIC ANTAGONIST

被引：160

作者：

LAMBRECHT, G ^{[1
]}

FEIFEL, R ^{[1
]}

FORTH, B ^{[1
]}

STROHMANN, C ^{[1
]}

TACKE, R ^{[1
]}

MUTSCHLER, E ^{[1
]}

机构：

[1] TECH UNIV BRUNSWICK,INST INORGAN & ANALYT CHEM,D-3300 BRUNSWICK,FED REP GER

来源：

EUROPEAN JOURNAL OF PHARMACOLOGY | 1988年 / 152卷 / 1-2期

关键词：

D O I：

10.1016/0014-2999(88)90856-4

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

收藏

页码：193 / 194

页数：2

相关论文

共 5 条

[1] ELTZE M, 1988, Naunyn-Schmiedeberg's Archives of Pharmacology, V337, pR91
[2] MUSCARINIC M1-RECEPTOR AND M2-RECEPTOR MEDIATING OPPOSITE EFFECTS ON NEUROMUSCULAR-TRANSMISSION IN RABBIT VAS-DEFERENS
ELTZE, M
[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 151 (02) : 205 - 221
[3] ANTIMUSCARINIC ACTION OF METHOCTRAMINE, A NEW CARDIOSELECTIVE M-2 MUSCARINIC RECEPTOR ANTAGONIST, ALONE AND IN COMBINATION WITH ATROPINE AND GALLAMINE
MELCHIORRE, C
ANGELI, P
LAMBRECHT, G
MUTSCHLER, E
PICCHIO, MT
WESS, J
[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1987, 144 (02) : 117 - 124
[4] MUTSCHLER E, 1987, INT C SERIES, V750, P67
[5] 80-PERCENT OF MUSCARINIC RECEPTORS EXPRESSED BY THE NB-OK 1 HUMAN NEURO-BLASTOMA CELL-LINE SHOW HIGH-AFFINITY FOR PIRENZEPINE AND ARE COMPARABLE TO RAT HIPPOCAMPUS M1 RECEPTORS
WAELBROECK, M
CAMUS, J
TASTENOY, M
CHRISTOPHE, J
[J]. FEBS LETTERS, 1988, 226 (02) : 287 - 290