MUSCARINIC ACTIVITY OF MCN-A-343 AND ITS VALUE IN MUSCARINIC RECEPTOR CLASSIFICATION

被引：75

作者：

EGLEN, RM ^{[1
]}

KENNY, BA ^{[1
]}

MICHEL, AD ^{[1
]}

WHITING, RL ^{[1
]}

机构：

[1] HERIOT WATT UNIV,SYNTEX RES CTR,DEPT PHARMACOL,EDINBURGH EH14 4AS,MIDLOTHIAN,SCOTLAND

来源：

BRITISH JOURNAL OF PHARMACOLOGY | 1987年 / 90卷 / 04期

关键词：

D O I：

10.1111/j.1476-5381.1987.tb11222.x

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：693 / 700

页数：8

共 50 条

[1] PHARMACOLOGY OF SELECTIVE MUSCARINIC LIGANDS RELATED TO MCN-A-343
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WEHRLE, J
HACKSELL, U
NILSSON, BM
TUMIATTI, V
LAMBRECHT, G
MUTSCHLER, E
[J]. LIFE SCIENCES, 1995, 56 (11-12) : 1006 - 1006
[2] DUAL EFFECT OF THE MUSCARINIC AGONIST MCN-A-343 ON VASCULAR NEUROEFFECTOR TRANSMISSION
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[J]. ACTA PHARMACOLOGICA ET TOXICOLOGICA, 1981, 49 (05): : 354 - 365
[3] Investigating the interaction of McN-A-343 with the M2 muscarinic receptor using its nitrogen mustard derivative
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[J]. BIOCHEMICAL PHARMACOLOGY, 2010, 79 (07) : 1025 - 1035
[4] McN-A-343 increases renal sympathetic nerve activity and blood pressure by a muscarinic and a non-muscarinic mechanism in the rat
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[J]. JOURNAL OF AUTONOMIC PHARMACOLOGY, 1996, 16 (05): : 281 - 292
[5] THE EFFECT OF MCN-A-343 ON MUSCARINIC RECEPTORS IN THE CEREBRAL-CORTEX AND HEART
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[J]. BRITISH JOURNAL OF PHARMACOLOGY, 1983, 78 (02) : 257 - 259
[6] Pressor effect of the putative M(1) muscarinic receptor agonist McN-A-343 in the conscious rat
Martin, JR
[J]. LIFE SCIENCES, 1996, 59 (22) : 1839 - 1852
[7] FUNCTIONAL DETERMINATION OF MCN-A-343 AFFINITY FOR M1 MUSCARINIC RECEPTORS
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[J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 1990, 253 (01): : 310 - 314
[8] EFFECTS OF MCN-A-343 ON INSECT NEUROSECRETORY-CELLS - EVIDENCE FOR MUSCARINIC-LIKE RECEPTOR SUBTYPES
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[J]. NEUROSCIENCE LETTERS, 1992, 139 (02) : 165 - 168
[9] MODULATION BY THE MUSCARINIC AGONIST MCN-A-343 OF NORADRENALINE RELEASE FROM VASCULAR SYMPATHETIC NEURONS
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[J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1980, 2 (05) : 629 - 643
[10] Investigating the interaction of McN-A-343 with the M1 muscarinic receptor using its nitrogen mustard derivative and ACh mustard
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