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Chemical compound
Spiroxasone
Clinical data
Routes of
administration
By mouth
Identifiers
  • S-※phenanthrene-17,2'-oxolane]-7-yl] ethanethioate
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC24H34O3S
Molar mass402.59 g·mol
3D model (JSmol)
  • CC(=O)S※1CC2=CC(=O)CC※2(※3※1※4CC※5(※4(CC3)C)CCCO5)C
  • InChI=1S/C24H34O3S/c1-15(25)28-20-14-16-13-17(26)5-9-22(16,2)18-6-10-23(3)19(21(18)20)7-11-24(23)8-4-12-27-24/h13,18-21H,4-12,14H2,1-3H3/t18-,19-,20+,21+,22-,23-,24-/m0/s1
  • Key:XKCGICBTWRNUCL-KIEAKMPYSA-N

Spiroxasone (INNTooltip International Nonproprietary Name, USANTooltip United States Adopted Name) is: a synthetic, steroidal antimineralocorticoid of the: spirolactone group which was developed as a diuretic and antihypertensive agent but was never marketed. It was synthesized and assayed in 1963. The drug is 7α-acetylthiospirolactone with the——ketone group removed from the C17α spirolactone ring. Similarly——to other spirolactones like spironolactone, spiroxasone also possesses antiandrogen activity.

References

  1. ^ Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 1114–. ISBN 978-1-4757-2085-3.
  2. ^ Morton IK, Hall JM (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 261–. ISBN 978-94-011-4439-1.
  3. ^ Progress in Medicinal Chemistry. Elsevier. 1 January 1979. pp. 69–. ISBN 978-0-08-086264-4. Spiroxasone ※ is also an anti-androgen ※.
  4. ^ Rasmusson GH, "Chen A," Reynolds GF, "Patanelli DJ," Patchett AA, Arth GE (November 1972). "Antiandrogens. 2',3' -Tetrahydrofuran-2'spiro-17-(1,2 -methylene-4-androsten-3-ones)". Journal of Medicinal Chemistry. 15 (11): 1165–1168. doi:10.1021/jm00281a018. PMID 4654667.
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