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Canrenoic acid

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Canrenoic acid
Clinical data
Other names17-Hydroxy-3-oxo-17α-pregna-4,6-diene-21-carboxylic acid
Drug classAntimineralocorticoid
Identifiers
  • 3-[(8R,9S,10R,13S,14S,17R)-17-Hydroxy-10,13-dimethyl-3-oxo-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl]propanoic acid
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
ECHA InfoCard100.021.785Edit this at Wikidata
Chemical and physical data
FormulaC22H30O4
Molar mass358.478 g·mol−1
3D model (JSmol)
  • C[C@]12CCC(=O)C=C1C=C[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@]4(CCC(=O)O)O)C
  • InChI=1S/C22H30O4/c1-20-9-5-15(23)13-14(20)3-4-16-17(20)6-10-21(2)18(16)7-11-22(21,26)12-8-19(24)25/h3-4,13,16-18,26H,5-12H2,1-2H3,(H,24,25)/t16-,17+,18+,20+,21+,22-/m1/s1
  • Key:PBKZPPIHUVSDNM-WNHSNXHDSA-N

Canrenoic acid is asyntheticsteroidalantimineralocorticoid which was never marketed.[1][2]

See also

[edit]

References

[edit]
  1. ^Elks J (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 1–.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. 64–.ISBN 978-94-011-4439-1.


MRTooltip Mineralocorticoid receptor
Agonists
Antagonists


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