
Spironolactone
Spironolactone is a steroid lactone that is 17alpha-pregn-4-ene-21,17-carbolactone substituted by an oxo group at position 3 and an alpha-acetylsulfanyl group at position 7. It has a role as a diuretic, an antihypertensive agent, a xenobiotic, an aldosterone antagonist and an environmental contaminant. It is a steroid lactone, an oxaspiro compound, a 3-oxo-Delta(4) steroid and a thioester. — ChEBI
- IUPAC name
- S-[(7R,8R,9S,10R,13S,14S,17R)-10,13-dimethyl-3,5'-dioxospiro[2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-7-yl] ethanethioate
- Molecular formula
- C24H32O4S
- Molecular weight
- 416.6 g/mol
- Exact mass
- 416.20213067 Da
- XLogP3
- 2.9
- Topological polar surface area
- 85.7 Ų
- Hydrogen-bond donors
- 0
- Hydrogen-bond acceptors
- 5
- Covalent units
- 1
- Defined stereocentres
- 7
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:9241
- ChEMBL:CHEMBL1393
- EPA DTXSID:DTXSID6034186
- PubMed:31065620
- PubMed:28024992
- PubMed:23116347
- PubMed:23105506
- PubMed:23077889
- PubMed:23077888
- PubMed:23077601
- PubMed:23074496
- PubMed:23074464
- PubMed:23060371
- PubMed:23035601
- PubMed:23031616
Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.