Structure via PubChem · Public domain (PubChem)
potassium canrenoate
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In the Vinony graph
Within Vinony's link graph, potassium canrenoate is referenced by 890 other articles, and connects out to intravenous infusion and defusion, route of administration and mometasone furoate.
It sits within the topics 11β-Hydroxylase inhibitors, Antimineralocorticoids and CYP17A1 inhibitors.
Its subject is documented across 8 Wikipedia language editions.
Chemical data
- Formula
- C22H29KO4
- Molecular weight
- 396.6 g/mol
- IUPAC name
- potassium 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]propanoate
- 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.[K+]
- InChIKey
- JTZQCHFUGHIPDF-RYVBEKKQSA-M
- Polar surface area
- 77.4 Ų
- H-bond donors
- 1
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 396.170291088
- Has use
- medication
Show 5 more facts
- chemical formula
- C₂₂H₂₉KO₄
- defined daily dose
- 0.4
- Commons category
- Potassium canrenoate
- isomeric SMILES
- [K+].[H][C@@]12CC[C@@](O)(CCC([O-])=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])C=CC2=CC(=O)CC[C@]12C
- canonical SMILES
- CC12CCC(=O)C=C1C=CC1C2CCC2(C)C1CCC2(O)CCC(=O)[O-].[K+]
Sources (2)
via Wikidata · CC0
Available in 8 languages
via Wikidata sitelinks · CC0
Categories
11β-Hydroxylase inhibitorsAntimineralocorticoidsCYP17A1 inhibitorsDrugboxes which contain changes to verified fieldsDrugboxes which contain changes to watched fieldsDrugs with no legal statusECHA InfoCard ID from WikidataPotassium compoundsPregnanesProdrugsProgestogensSpirolactonesSteroidal antiandrogens