Weight | 362.407 g/mol |
---|---|
Formula | C17H18N2O5S |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 5 |
piretanide (55837-27-9)
HOE 118 · 4-phenoxy-3-pyrrolidin-1-yl-5-sulfamoylbenzoic acid
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- Inhibition of active chloride transport by piretanide. (Nature, 1978)
- Buoyancy and Drug Release Patterns of Floating Minitablets Containing Piretanide and Atenolol as Model Drugs (Pharmaceutical Development and Technology, 1998)
- K+-induced swelling of vestibular dark cells is dependent on Na+ and Cl and inhibited by piretanide (Pflgers Archiv: European Journal of Physiology, 1990)
- Effects of piretanide, bumetanide and frusemide on electrolyte and urate excretion in normal subjects. (British Journal of Clinical Pharmacology, 1978)
- Kinetic and dynamic comparison of piretanide and furosemide. (Clinical Pharmacology & Therapeutics, 1978)
- Electrochemical determination of the loop diuretics piretanide and furosemide in pharmaceutical formulations and urine (Analytica Chimica Acta, 1995)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - HOE 118
- 4-phenoxy-3-pyrrolidin-1-yl-5-sulfamoylbenzoic acid
-
SMILESC1CCN(C1)C2=C(C(=CC(=C2)C(=O)O)S(=O)(=O)N)OC3=CC=CC=C3
-
InChIKeyUJEWTUDSLQGTOA-UHFFFAOYSA-N
- Pubchem - piretanide
- Wikipedia - piretanide
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 medication in Germany, France, Italy and other countries.
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