McN-A-343

Known as: McN A-343, McN A343, McNA343 
 
National Institutes of Health

Papers overview

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Review
2012
Review
2012
The unusual pharmacology of McN-A-343 was first described by Roszowski in 1961. The agonist appeared to be a selective stimulant… (More)
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Highly Cited
2006
Highly Cited
2006
TNF has a critical mediator role in inflammation and is an important therapeutic target. We recently discovered that TNF… (More)
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Highly Cited
2001
Highly Cited
2001
Medium spiny neurons were recorded from striatal slices obtained from mice lacking the group I metabotropic glutamate receptor… (More)
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2000
2000
BACKGROUND We employed modern statistical and data mining methods to model survival based on preoperative and intraoperative… (More)
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1997
1997
The mode of interaction of the muscarinic M2 receptor partial agonist, McN-A-343 (4-(m-chlorophenylcarbamoyloxy)-2… (More)
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1990
1990
The affinity (KA) of 4-(m-chlorophenyl-carbamoyloxy)-2-butynyltrimethylammonium chloride (McN-A-343), acting as an agonist of M1… (More)
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1990
1990
The potency and efficacy of McN-A-343 (McN) in stimulating phosphoinositide (PI) hydrolysis were investigated in Chinese hamster… (More)
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1987
1987
The affinity and potency of McN-A-343 (4-(m-chlorophenyl-carbamoyloxy) -2-butynyltrimethylammonium chloride) has been assessed at… (More)
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1985
1985
Intracellular recordings were made from guinea-pig myenteric and submucous plexus neurones. Nicotinic excitatory post-synaptic… (More)
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1983
1983
McN-A-343 behaves as a competitive agonist in binding to muscarinic receptors in the cerebral cortex. In its interaction with… (More)
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