Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C23H32O4S |
Molecular Weight | 404.563 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 8 / 8 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CS[C@@H]1[C@@H](O)C2=CC(=O)CC[C@]2(C)[C@H]3CC[C@@]4(C)[C@@H](CC[C@@]45CCC(=O)O5)[C@H]13
InChI
InChIKey=NWLBSWATTSRBOV-DFSNYPBXSA-N
InChI=1S/C23H32O4S/c1-21-8-4-13(24)12-16(21)19(26)20(28-3)18-14(21)5-9-22(2)15(18)6-10-23(22)11-7-17(25)27-23/h12,14-15,18-20,26H,4-11H2,1-3H3/t14-,15-,18+,19-,20-,21+,22-,23+/m0/s1
Molecular Formula | C23H32O4S |
Molecular Weight | 404.563 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 8 / 8 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:28:32 GMT 2025
by
admin
on
Mon Mar 31 23:28:32 GMT 2025
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Record UNII |
4A93WO4Z3G
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Record Status |
Validated (UNII)
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Record Version |
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-
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4A93WO4Z3G
Created by
admin on Mon Mar 31 23:28:32 GMT 2025 , Edited by admin on Mon Mar 31 23:28:32 GMT 2025
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DTXSID00962376
Created by
admin on Mon Mar 31 23:28:32 GMT 2025 , Edited by admin on Mon Mar 31 23:28:32 GMT 2025
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6?-Hydroxy-7?-thiomethylspironolactone
Created by
admin on Mon Mar 31 23:28:32 GMT 2025 , Edited by admin on Mon Mar 31 23:28:32 GMT 2025
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42219-60-3
Created by
admin on Mon Mar 31 23:28:32 GMT 2025 , Edited by admin on Mon Mar 31 23:28:32 GMT 2025
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40580543
Created by
admin on Mon Mar 31 23:28:32 GMT 2025 , Edited by admin on Mon Mar 31 23:28:32 GMT 2025
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Related Record | Type | Details | ||
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PRODRUG -> METABOLITE ACTIVE |
The pharmacological activity of spironolactone metabolites in man is not known. However, in the adrenalectomized rat the antimineralocorticoid activities of the metabolites C, TMS, and HTMS, relative to spironolactone, were 1.10, 1.28, and 0.32, respectively.
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PARENT -> METABOLITE |