18-substituted Steroids--9[1]. Studies on the Stability of Aldosterone in Dilute Alkali
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In the presence of dilute alkali at room temperature aldosterone undergoes rearrangement to form an isomeric compound identified as 11 beta, 18;18,21-diepoxy-20,21-dihydroxypregn-4-en-3-one. The presence of dissolved oxygen causes simultaneous degradation to form 11 beta, 18-epoxy-18-hydroxy-3-oxo-17(beta H)-androst-4-ene-17 alpha-carboxylic acid. Under similar alkaline conditions at reflux temperature in aqueous methanol aldosterone undergoes rearrangement to form (20S)-20,21-dihydroxy-3-oxo-pregn-4-eno-18,11 beta-lactone accompanied by an intramolecular aldol type condensation to form 11 beta, 21-dihydroxy-18,21-cyclopregna-4,18(21)-diene-3,20-dione. Identical products were formed from 17-isoaldosterone. The mechanisms of these reactions are discussed.
Singh N, Taibon J, Pongratz S, Geletneky C RSC Adv. 2022; 11(38):23627-23630.
PMID: 35479823 PMC: 9036601. DOI: 10.1039/d1ra03472c.
Aldosterone metabolism in rat renal tissue in vitro. Formation of lipid soluble metabolites.
lAllemand D, Siebe H, Tsiakiras D, Hoyer G, Vecsei P, HIERHOLZER K Pflugers Arch. 1988; 411(5):529-39.
PMID: 3387188 DOI: 10.1007/BF00582374.