Weight | 358.478 g/mol |
---|---|
Formula | C22H30O4 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
Canrenoic acid (4138-96-9)
Potassium Canrenoate · Canrenoate Potassium · Soldactone
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- Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) "probes" for human udp-glucuronosyltransferases. (Drug Metabolism and Disposition, 2005)
- Randomized clinical study of the efficacy of amiloride and potassium canrenoate in nonazotemic cirrhotic patients with ascites (Hepatology, 1994)
- Spironolactone and Its Main Metabolite, Canrenoic Acid, Block Human Ether-a-Go-Go-Related Gene Channels (Circulation, 2003)
- Pharmacokinetic and Metabolic Fate of Potassium Canrenoate (SC-14266) in Man (Journal of Pharmaceutical Sciences, 1971)
- Spironolactone and potassium canrenoate in normal man. (Clinical Pharmacology & Therapeutics, 1976)
- Conversion of spironolactone to canrenone and disposition kinetics of spironolactone and canrenoate-potassium in rats. (Naunyn-schmiedebergs Archives of Pharmacology, 1974)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Potassium Canrenoate
- Canrenoate Potassium
- Soldactone
- 17-Hydroxy-3-Oxo-17alpha-Pregna-4,6-Diene-21-Carboxylic Acid
- Pfizer Brand of Canrenoate Potassium
- Kalium-Can.-ratiopharm
- ratiopharm Brand of Canrenoate Potassium
- Boehringer Mannheim Brand of Canrenoate Potassium
- SC-14266
- 17 Hydroxy 3 Oxo 17alpha Pregna 4,6 Diene 21 Carboxylic Acid
- SC14266
- Soludactone
- Spiroctan
- SC 14266
-
SMILESCC12CCC(=O)C=C1C=CC3C2CCC4(C3CCC4(CCC(=O)O)O)C
-
InChIKeyPBKZPPIHUVSDNM-UHFFFAOYSA-N
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