Prorenone
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| Other names | SC-23133; 3-(17β-Hydroxy-6β,7β-methylene-3-oxo-4-androsten-17α-yl)propionic acid γ-lactone |
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| Formula | C23H30O3 |
| Molar mass | 354.48 g/mol g·mol−1 |
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Prorenone (developmental code name SC-23133) is a steroidal antimineralocorticoid of the spirolactone group related to spironolactone that was never marketed.[1] It is the lactonic form of prorenoic acid (prorenoate), and prorenoate potassium (SC-23992), the potassium salt of prorenoic acid, also exists.[1] Prorenoate potassium is about 8 times more potent than spironolactone as an antimineralocorticoid in animals, and it may act as a prodrug to prorenone.[1] In addition to the mineralocorticoid receptor, prorenone also binds to the glucocorticoid, androgen, and progesterone receptors.[2] Similarly to spironolactone, prorenone is also a potent inhibitor of aldosterone biosynthesis.[3]
Chemical synthesis
Prorenone can be synthesized via a Johnson–Corey–Chaykovsky reaction by reaction of canrenone with trimethylsulfonium iodide and sodium hydride.[4]
See also
References
- ^ a b c Claire, M.; Rafestin-Oblin, M. E.; Michaud, A.; Roth-Meyer, C.; Corvol, P. (1979). "Mechanism of Action of a New Antialdosterone Compound, Prorenone*". Endocrinology. 104 (4): 1194–1200. doi:10.1210/endo-104-4-1194. ISSN 0013-7227.
- ^ Gyorgy Szasz; Zsuzsanna Budvari-Barany (19 December 1990). Pharmaceutical Chemistry of Antihypertensive Agents. CRC Press. pp. 87–. ISBN 978-0-8493-4724-5.
- ^ Netchitailo, Pierre; Delarue, Catherine; Perroteau, Isabelle; Leboulenger, Francois; Capron, Michel-Hubert; Vaudry, Hubert (1985). "Relative inhibitory potency of five mineralocorticoid antagonists on aldosterone biosynthesis in vitro". Biochemical Pharmacology. 34 (2): 189–194. doi:10.1016/0006-2952(85)90123-6. ISSN 0006-2952.
- ^ Chinn, L.; 1974, U.S. patent 3,845,041
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