Piretanide
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Trade names | Arelix, Eurelix, Tauliz |
AHFS/Drugs.com | International Drug Names |
Routes of administration | Oral |
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E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
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Formula | C17H18N2O5S |
Molar mass | 362.40 g/mol |
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WikiDoc Resources for Piretanide |
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Ongoing Trials on Piretanide at Clinical Trials.gov Clinical Trials on Piretanide at Google
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US National Guidelines Clearinghouse on Piretanide
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Piretanide (INN, trade names Arelix, Eurelix, Tauliz) has been synthesized in 1973 at Hoechst AG (Germany) as a loop diuretic compound by using a then-new method for introducing cyclic amine residues in an aromatic nucleus in the presence of other aromatically bonded functional groups. Studies of piretanide in rats and dogs in comparison with other high-ceiling diuretics such as furosemide and bumetanide found a more suitable dose/response rate (regression line) and a more favourable sodium/potassium excretion ratio. These findings led eventually to clinical studies in man and finally to the introduction as a saluretic and antihypertensive[1] medication in Germany, France, Italy and other countries.
References
- ↑ Haberfeld, H, ed. (2009). Austria-Codex (in German) (2009/2010 ed.). Vienna: Österreichischer Apothekerverlag. ISBN 3-85200-196-X.
- W.Merkel, D.Bormann, D.Mania, R.Muschaweck and M.Hropot, Eur. J. Med. Chem.-Chim.Ther. 11,399 (1976).
- W.Merkel, D.Mania and D.Bormann, Liebigs Ann. Chem. 461 (1979).
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