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halopemide

Known as: N-(2-(4-(5-chloro-2-oxo-1-benzimidazolinyl)piperidino)ethyl)-p-fluorobenzamide 
 
National Institutes of Health

Papers overview

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2014
2014
Further chemical optimization of the halopemide-derived family of dual phospholipase D1/2 (PLD1/2) inhibitors afforded ML395… Expand
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2009
2009
Dialkylamino-alkyl-benzamides possess an affinity for melanin, suggesting that labeling of such benzamides with 18F could… Expand
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Highly Cited
2007
Highly Cited
2007
Halopemide, which was identified by HTS to inhibit phospholipase D2 (PLD2), provided the basis for an exploratory effort to… Expand
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1984
1984
The resocializing and activating properties of halopemide were investigated in an open study and a double-blind study in 20… Expand
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1981
1981
Oxiperomide and tiapride are dopamine receptor antagonists claimed to have “antidyskinetic” properties in animal models and in… Expand
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1981
1981
The recently developed psychotropic agent halopemide (R 34301) has a unique pharmacological and clinical profile11,1~. Although… Expand
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1980
1980
The effects of halopemide on the release of 3H-serotonin, 3H-noradrenaline, 3H-acetylcholine and 3H-GABA from rat frontal… Expand
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1979
1979
Dynamic (solvent generated) cation-exchange systems for the separation of drugs and main metabolites derived from butyrophenone… Expand
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1978
1978
Halopemide is a new psychotropic agent, structurally related to the neuroleptics of the butyrophenone type, but with a different… Expand
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1978
1978
Abstract Various dopamine antagonists, including two novel non-neuroleptic drugs domperidone and halopemide, stimulated… Expand
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