THC Science

Canrenoic acid
Clinical data
Other names	17-Hydroxy-3-oxo-17α-pregna-4,6-diene-21-carboxylic acid
Drug class	Antimineralocorticoid
Identifiers
	IUPAC name 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	4138-96-9;
PubChem CID	656615;
ChemSpider	570976;
UNII	87UG89VA9K;
CompTox Dashboard (EPA)	DTXSID5022726 ;
ECHA InfoCard	100.021.785
Chemical and physical data
Formula	C22H30O4
Molar mass	358.478 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES 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 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 a synthetic steroidal antimineralocorticoid which was never marketed.^[1]^[2]

References[edit]

^ 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.
^ 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.