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haloalkylamine

 
National Institutes of Health

Papers overview

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2009
2009
The haloalkylamine DSP4 (N[-2-chloroethyl]-N-ethyl-2-bromobenzylamine) is a noradrenergic neurotoxin, which is used for the… Expand
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1991
1991
The haloalkylamine 2-bromoethanamine (BEA) causes necrosis of renal papillae of rats within 24 h of a single intraperitoneal dose… Expand
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1988
1988
A series of tertiary 3- and 4-haloalkylamines related to the muscarinic agent oxotremorine was synthesized. The compounds… Expand
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1983
1983
The interaction of beta-haloalkylamine derivatives of dopamine agonists and antagonists with 3H-spiperone binding (D2 sites) and… Expand
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1980
1980
Abstract The haloalkylamine N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine hydrochloride (DSP 4), impairs the ability of central… Expand
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1977
1977
1. The pharmacological characteristics of adrenoceptors at different temperatures were assessed on the basis of the effects of… Expand
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1975
1975
1 The role of the uptake and release of agonist from extraneuronal sites in the termination of responses of rabbit aortic strips… Expand
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1972
1972
1. Twenty-one haloalkylamine derivatives were tested as inhibitors of both the neuronal uptake of (3)H-noradrenaline (NA) by the… Expand
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1969
1969
1. The mechanisms by which a haloalkylamine (GD-131) alters the inactivation of and potentiates responses to certain… Expand
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1952
1952
The relative ability of various aryl-2-haloalkylamine adrenergic blocking drugs to block the spasmogenic effects of equi… Expand
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