U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
This repository is under review for potential modification in compliance with Administration directives.

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
Structure of 6.BETA.-HYDROXY-7.ALPHA.-THIOMETHYLSPIROLACTONE

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

HIDE SMILES / InChI

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 Mon Mar 31 23:28:32 GMT 2025
Edited
by admin
on Mon Mar 31 23:28:32 GMT 2025
Record UNII
4A93WO4Z3G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6.BETA.-HYDROXY-7.ALPHA.-THIOMETHYLSPIROLACTONE
Common Name English
3-(3-OXO-7.ALPHA.-METHYLTHIO-6.BETA.,17.BETA.-DIHYDROXY-4-ANDROSTEN-17.ALPHA.-YL)PROPIONIC ACID .GAMMA. LACTONE
Preferred Name English
6.BETA.-HYDROXY-7.ALPHA.-(THIOMETHYL)SPIROLACTONE
Common Name English
6.BETA.,17-DIHYDROXY-7.ALPHA.-METHYLTHIO-3-OXO-17.ALPHA.-PREGN-4-ENE-21-CARBOXYLIC ACID .GAMMA.-LACTONE
Common Name English
6.BETA.-HYDROXY-7.ALPHA.-(METHYLTHIO)SPIROLACTONE
Common Name English
SPIRONOLACTONE METABOLITE M5
Common Name English
6-HYDROXY-7-THIOMETHYLSPIROLACTONE
Common Name English
(7S,8R,9S,10R,13S,14S,17R)-6-HYDROXY-10,13-DIMETHYL-7-METHYLSULFANYL-SPIRO(2,6,7,8,9,11,12,14,15,16-DECAHYDRO-1H-CYCLOPENTA(A)PHENANTHRENE-17,5'-TETRAHYDROFURAN)-2',3-DIONE
Systematic Name English
Code System Code Type Description
FDA UNII
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
PRIMARY
EPA CompTox
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
PRIMARY
WIKIPEDIA
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
PRIMARY
CAS
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
PRIMARY
PUBCHEM
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
PRIMARY
Related Record Type Details
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.
PARENT -> METABOLITE