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Prorenoate potassium

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Prorenoate potassium
Clinical data
Other namesSC-23992; 6α,7α-Dihydro-17-hydroxy-3-oxo-3'H-cyclopropa(6,7)-17α-pregna-4,6-diene-21-carboxylic acid monopotassium salt
Drug classAntimineralocorticoid
Identifiers
  • Potassium 3-[(1aR,5aR,5bS,7aS,8R,10aS,10bR,10cR)-8-hydroxy-5a,7a-dimethyl-3-oxo-1,1a,3,4,5,5a,5b,6,7,7a,8,9,10,10a,10b,10c-hexadecahydrocyclopenta[a]cyclopropa[l]phenanthren-8-yl]propanoate
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC23H31KO4
Molar mass410.595 g·mol−1
3D model (JSmol)
  • C[C@]12CCC(=O)C=C1[C@@H]3C[C@@H]3[C@@H]4[C@@H]2CC[C@]5([C@H]4CC[C@]5(CCC(=O)[O-])O)C.[K+]
  • InChI=1S/C23H32O4.K/c1-21-7-3-13(24)11-18(21)14-12-15(14)20-16(21)4-8-22(2)17(20)5-9-23(22,27)10-6-19(25)26;/h11,14-17,20,27H,3-10,12H2,1-2H3,(H,25,26);/q;+1/p-1/t14-,15+,16+,17+,20-,21-,22+,23-;/m1./s1
  • Key:NLSAMWIBIQWHTK-CZKUEYQYSA-M

Prorenoate potassium (developmental code nameSC-23992) 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. 1036–.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. 234–.ISBN 978-94-011-4439-1.


MRTooltip Mineralocorticoid receptor
Agonists
Antagonists


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