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3-[(1S,2R,10R,11S,14R,15S)-14-hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-6,8-dien-14-yl]propanoic acid potassium
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ChemBase ID:
133428
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Molecular Formular:
C22H30KO4
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Molecular Mass:
397.5695
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Monoisotopic Mass:
397.17811612
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SMILES and InChIs
SMILES:
C[C@]12CCC(=O)C=C1C=C[C@@H]1[C@@H]2CC[C@]2([C@H]1CC[C@]2(CCC(=O)O)O)C.[K]
Canonical SMILES:
OC(=O)CC[C@]1(O)CC[C@@H]2[C@]1(C)CC[C@H]1[C@H]2C=CC2=CC(=O)CC[C@]12C.[K]
InChI:
InChI=1S/C22H30O4.K/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
InChIKey:
OCNCAPJTFQNUKP-RYVBEKKQSA-N
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Cite this record
CBID:133428 http://www.chembase.cn/molecule-133428.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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3-[(1S,2R,10R,11S,14R,15S)-14-hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-6,8-dien-14-yl]propanoic acid potassium
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IUPAC Traditional name
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Synonyms
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17-Hydroxy-3-oxopregna-4,6-diene-21-carboxylic acid
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Potassium canrenoate
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Canrenoic acid potassium salt
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(17α)-17-Hydroxy-3-oxopregna-4,6-diene-21-carboxylic Acid Potassium Salt
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Aldadiene Kalium
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Aldadiene Potassium
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CB 8109
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Canrenoate Potassium
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Kanrenol
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MF 465 a
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Potassium 17-Hydroxy-3-oxo-17α-pregna-4,6-diene-21-carboxylate
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Potassium 3-(17β-Hydroxy-3-oxoandrosta-4,6-dien-17-yl)propionate
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Potassium 3-(3-oxo-17β-hydroxy-4,6-androstadien-17α-yl)propionate
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Potassium Aldadiene
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Potassium β-(3-Oxo-17β-hydroxyandrosta-4,6-dien-17α-yl)Propionate
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SC 14266
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SC 14266/371
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Soldactona
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Soldactone
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Soludactone
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Venactone
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Canrenoic Acid Potassium Salt
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CAS Number
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EC Number
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MDL Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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4.480851
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H Acceptors
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4
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H Donor
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2
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LogD (pH = 5.5)
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1.8734317
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LogD (pH = 7.4)
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0.106526814
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Log P
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2.9309275
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Molar Refractivity
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100.975 cm3
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Polarizability
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39.05853 Å3
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Polar Surface Area
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74.6 Å2
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Rotatable Bonds
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3
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
Sigma Aldrich
TRC
Sigma Aldrich -
C7287
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Quality Aqueous solutions may contain some insoluble material. Biochem/physiol Actions Competitive aldosterone receptor antagonist. Potassium canrenoate reduces the effects of aldosterone-induced increases in blood pressure and in cardiovascular fibrosis in animals with high sodium intake. It is used clinically for its anti-fibrotic effects. At higher doses it is genotoxic to liver and increases tumor incidence in rodent models. |
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Sadee, W., et al.: J. Pharm. Sci., 61, 1126 (1972)
- • Peterfalvi, M., et al.: Biochem. Pharmacol., 29, 353 (1972)
- • Los, L., et al.: Drug Metab. Dispos., 21, 1086 (1972)
- • Ter Heine, R., et al.: J. Pharm. Biomed. Anal., 49, 451 (1972)
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PATENTS
PATENTS
PubChem Patent
Google Patent