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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H32O3
Molecular Weight 332.477
Optical Activity ( + )
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Epiandrosterone acetate

SMILES

CC(=O)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@H]23)C1

InChI

InChIKey=FDCINQSOYQUNKB-HGDYXINXSA-N
InChI=1S/C21H32O3/c1-13(22)24-15-8-10-20(2)14(12-15)4-5-16-17-6-7-19(23)21(17,3)11-9-18(16)20/h14-18H,4-12H2,1-3H3/t14-,15-,16-,17-,18-,20-,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H32O3
Molecular Weight 332.477
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:49:59 GMT 2025
Edited
by admin
on Mon Mar 31 21:49:59 GMT 2025
Record UNII
MT8537SW7X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Epiandrosterone acetate
Common Name English
NSC-120612
Preferred Name English
5?-Androstan-3?-ol-17-one acetate
Common Name English
3?-Acetoxy-5?-androstan-17-one
Common Name English
Androstan-17-one, 3-(acetyloxy)-, (3?,5?)-
Common Name English
[(3S,5S,8R,9S,10S,13S,14S)-10,13-dimethyl-17-oxo-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-3-yl] acetate
Systematic Name English
(3?,5?)-3-(Acetyloxy)androstan-17-one
Common Name English
epi-Androsterone acetate
Common Name English
Isoandrosterone acetate
Common Name English
17-Oxo-5?-androstan-3?-yl acetate
Common Name English
5?-Androstan-17-one, 3?-hydroxy-, acetate
Common Name English
Code System Code Type Description
PUBCHEM
908740
Created by admin on Mon Mar 31 21:49:59 GMT 2025 , Edited by admin on Mon Mar 31 21:49:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID601305364
Created by admin on Mon Mar 31 21:49:59 GMT 2025 , Edited by admin on Mon Mar 31 21:49:59 GMT 2025
PRIMARY
CAS
1239-31-2
Created by admin on Mon Mar 31 21:49:59 GMT 2025 , Edited by admin on Mon Mar 31 21:49:59 GMT 2025
PRIMARY
FDA UNII
MT8537SW7X
Created by admin on Mon Mar 31 21:49:59 GMT 2025 , Edited by admin on Mon Mar 31 21:49:59 GMT 2025
PRIMARY
NSC
120612
Created by admin on Mon Mar 31 21:49:59 GMT 2025 , Edited by admin on Mon Mar 31 21:49:59 GMT 2025
PRIMARY