tiaramide

Known as: 4-((5-chloro-2-oxo-3(2H)-benzothiazolyl)acetyl)- 1-piperazineethanol 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1974-2016
0519742016

Papers overview

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2002
2002
TSQ ESI MS/MS and ion trap ESI MS(2) cleave protonated molecules. MS(2) at m/z 332 of zotepine cleaved m/z 245 (10%), m/z 287 (5… (More)
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1989
1989
1. Metabolism of basic drugs may result in the formation of zwitterionic sulphate conjugates. The additional ionization… (More)
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1988
1988
The mechanism of bradykinin-induced contraction in rabbit urinary detrusor was investigated using an anti-inflammatory drug… (More)
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1986
1986
The site of the analgesic action of non-acidic (basic), non-steroidal anti-inflammatory drugs (NSAIDs) was investigated in the… (More)
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1985
1985
The mechanism by which tiaramide inhibited platelet aggregation was investigated using phospholipid labelling techniques by 14C… (More)
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1982
1982
1. N-Dealkylation and N-oxidation of tiaramide and of its major metabolite, TRAA, by human and rat liver microsomes were… (More)
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1982
1982
The disposition and metabolism of 14C-tiaramide HCl was examined in four healthy male volunteers, after administration of a 200… (More)
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1982
1982
1. The metabolism of tiaramide, 4-[(5-chloro-2-oxo-3(2H)-benzothiazolyl)acetyl]-1-piperazineethanol, was studied in healthy male… (More)
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1981
1981
Eighty patients took part in this double-blind, single-dose group-comparative study, comparing the analgesic efficacy of… (More)
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1977
1977
1. Urinary excretion of the radioactivity in 24 h after oral administration of [14C]tiaramide hydrochloride was 67% of the dose… (More)
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