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oxatomide

Known as: 1-(3-(4-(diphenylmethyl)-1-piperazinyl)propyl)-1,3-dihydro-2H-benzimidazol-2-one, oxatimide 
National Institutes of Health

Related topics

Related topics

6 relations

Broader (4)

Anti-Allergic AgentsAnti-Asthmatic AgentsHistamine H1 AntagonistsPiperazines

Narrower (2)

KW 4354Tinset

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2003
2003
Evaluation of the effects of anti-pruritic drugs on scratch responses using histamine H1 receptor-deficient mice.
1998
1998
Characterization of antihistamines using biphasic cutaneous reaction in BALB/c mice.
1997
1997
Effect of TYB-2285 on antigen-induced accumulation of eosinophils into the peritoneal cavity of rats sensitized with Ascaris suum extract.
1995
1995
Comparison of anti-allergic activities of the histamine H1 receptor antagonists epinastine, ketotifen and oxatomide in human leukocytes.
The effects of three histamine H1 receptor antagonists, epinastine (CAS 80012-43-7, WAL-801 CL), ketotifen (CAS 34580-13-7) and… 
1991
1991
Role of endoplasmic reticulum, an intracellular Ca2+ store, in histamine release from rat peritoneal mast cell.
1991
1991
Cetirizine, Oxatomide, Ketotifen and Placebo
SummaryAt 1-week intervals, 12 healthy volunteers received oral cetirizine 10mg, oxatomide 30mg, ketotifen 1mg or placebo under… 
1990
1990
Efficacy of topical oxatomide in women with pruritus vulvae.
Pruritus vulvae is a very common condition. The patient's scratching often worsens the situation and makes diagnosis by the… 
1987
1987
Calmodulin antagonism: a pharmacological approach for the inhibition of mediator release from mast cells.
1985
1985
Inhibitory effects of oxatomide on several activities of SRS-A and synthetic leukotrienes in guinea-pigs and rats.
Effects of oxatomide, an orally active anti-allergic drug, on several activities of slow reacting substance of anaphylaxis (SRS-A… 
1978
1978
Protection of rats from compound 48/80-induced lethality. A simple test for inhibitors of mast cell-mediated shock.
The dose of 0.5 mg/kg i.v. of compound 48/80 was lethal in 97.2% of the injected rats. Observations before death and at autopsy… 
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