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Burimamide

Known as: Burimamide [Chemical/Ingredient], Thiourea, N-(4-(1H-imidazol-4-yl)butyl)-N'-methyl- 
An antagonist of histamine that appears to block both H2 and H3 histamine receptors. It has been used in the treatment of ulcers.
National Institutes of Health

Related topics

Related topics

9 relations

Broader (2)

Anti-Ulcer AgentHistamine H2 Antagonists
In Bloodagonistsanalogs & derivativesantagonists & inhibitors

Papers overview

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1980
1980
Excitatory and inhibitory effects of histamine on molluscan neurons
1979
1979
LIVER ALCOHOL AND ALDEHYDE DEHYDROGENASE: INHIBITION AND POTENTIATION BY HISTAMINE AGONISTS AND ANTAGONISTS
1. The in vitro effects of histamine, some other Hi‐ and H2‐receptor agonists and some antagonists were studied on the specific… 
1977
1977
Effect of mepyramine, a histamine H1-, and burimamide, a histamine H2-receptor antagonist, on ovum implantation in the rat.
Systemic administration to rats of a combination of mepyramine, a histamine H1-, and burimamide, a histamine H2-receptor… 
1977
1977
Stimulation of cyclic adenosine 3′,5′-monophosphate in chick cerebral hemisphere slices: effects of H2 and H2 histaminergic agonists and antagonists
1977
1977
Effects of histamine on the human penis muscle in vitro.
1976
1976
Inhibition of paraquat accumulation in rat lung slices by a component of rat plasma and a variety of drugs and endogenous amines.
1976
1976
Histamine H2-receptor antagonists and thermal injury in rats
1975
1975
Occurrence of H2-receptors for histamine in the guinea-pig intestine.
1974
1974
A vasodepressor action of histamine mediated by H2-receptor activation.
1973
1973
Some effects of burimamide on the isolated perfused pulmonary circulation of the guinea‐pig
Infusions of burimamide were found to potentiate the pressor response to histamine and abolish the depressor response to… 
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