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Spironolactone is a steroidal aldosterone blocker that was by John A. Cella and Robert C. Tweit at G. D. Searle & Co.1 (Skokie, IL). Aldosterone is an essential corticosteroid hormone that conserves sodium in the kidneys and other organs and regulates blood pressure. But it must be suppressed to treat fluid buildup in patients with heart failure, high blood pressure, and other conditions.
Cella and Tweit鈥檚 article was the second in a series on novel aldosterone blockers. In the first article, they reported compounds that worked best when administered parenterally. Spironolactone and similar compounds showed improved blocking activity when administered orally.
Spironolactone is on the World Health Organization's List of Essential Medicines. To this day, it is prescribed more than ten million times a year in the United States. The drug, however, has numerous adverse side effects, including high blood potassium, nausea, frequent urination, and dehydration. It also has estrogen-like effects, which can decrease sex drive in men. In recent years, this estrogenic property has been useful in feminizing hormone therapy for transgender women.
1. Searle was acquired by Monsanto in 1985 and was eventually absorbed into Pfizer.
Spironolactone聽hazard information
Hazard class* | Hazard statement | |
---|---|---|
Acute toxicity, oral, category 4 | H302鈥擧armful if swallowed | ![]() |
Reproductive toxicity, category 1B | H360鈥擬ay damage fertility or the unborn child | ![]() |
聽*Globally Harmonized System of Classification and Labeling of Chemicals.
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Spironolactone fast facts
CAS Reg. No. | 52-01-7 |
nomenclature | Pregn-4-ene-21-carboxylic acid, 7-(acetylthio)-17-hydroxy-3-oxo-, 纬-lactone, (7伪,17伪)- |
Empirical formula | C24H32O4S |
Molar mass | 416.57 g/mol |
Appearance | White to light tan crystalline powder |
Melting Point | 134鈥�135 潞Ca |
Water solubility聽 | 22 mg/L |
a. Resolidifies and decomposes at 201鈥�208 潞C.

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