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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H26O3
Molecular Weight 302.4079
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 7-KETO-DEHYDROEPIANDROSTERONE

SMILES

C[C@]12CC[C@H]3[C@H]([C@@H]1CCC2=O)C(=O)C=C4C[C@@H](O)CC[C@]34C

InChI

InChIKey=KPRGOTLNGIBVFL-GINZOMEDSA-N
InChI=1S/C19H26O3/c1-18-7-5-12(20)9-11(18)10-15(21)17-13-3-4-16(22)19(13,2)8-6-14(17)18/h10,12-14,17,20H,3-9H2,1-2H3/t12-,13-,14-,17-,18-,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H26O3
Molecular Weight 302.4079
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Dehydroepiandrosterone 7alpha-hydroxylation in human tissues: possible interference with type 1 11beta-hydroxysteroid dehydrogenase-mediated processes.
2007-05
A novel radioimmunoassay of 7-oxo-DHEA and its physiological levels.
2007-04
Steroids and thermogenesis.
2006
How short-term transdermal treatment of men with 7-oxo-dehydroepiandrosterone influence thyroid function.
2006
Delayed effects of short-term transdermal application of 7-oxo-dehydroepiandrosterone on its metabolites, some hormonal steroids and relevant proteohormones in healthy male volunteers.
2005
Biosynthesis of [3H]7 alpha-hydroxy-, 7 beta-hydroxy-, and 7-oxo-dehydroepiandrosterone using pig liver microsomal fractions.
2004-10-01
[Effects of 7-oxo-DHEA treatment on the immunoreactivity of BALB/c mice subjected to chronic mild stress].
2003-12
Glucocorticoids inhibit interconversion of 7-hydroxy and 7-oxo metabolites of dehydroepiandrosterone: a role for 11beta-hydroxysteroid dehydrogenases?
2003-04-15
Ergosteroids V: preparation and biological activity of various D-ring derivatives in the 7-oxo-dehydroepiandrosterone series.
2002-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:38:45 GMT 2025
Edited
by admin
on Mon Mar 31 18:38:45 GMT 2025
Record UNII
2334LJD2E9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
7-KETO-DEHYDROEPIANDROSTERONE
WHO-DD  
Common Name English
7-KETO-DHEA
Preferred Name English
7-KETODEHYDROEPIANDROSTERONE
Common Name English
7-OXODEHYDROEPIANDROSTERONE
Common Name English
7-keto-dehydroepiandrosterone [WHO-DD]
Common Name English
ANDROST-5-ENE-7,17-DIONE, 3-HYDROXY-, (3.BETA.)-
Systematic Name English
7-OXO-PRASTERONE
Common Name English
7-OXO-DEHYDROEPIANDROSTERONE
Common Name English
Classification Tree Code System Code
DSLD 395 (Number of products:72)
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
Code System Code Type Description
MESH
C002914
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
FDA UNII
2334LJD2E9
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
WIKIPEDIA
7-KETO-DHEA
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
CAS
566-19-8
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
DAILYMED
2334LJD2E9
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
PUBCHEM
193313
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
EVMPD
SUB120413
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
SMS_ID
100000143492
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
RXCUI
1427084
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY RxNorm
EPA CompTox
DTXSID801024029
Created by admin on Mon Mar 31 18:38:45 GMT 2025 , Edited by admin on Mon Mar 31 18:38:45 GMT 2025
PRIMARY
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ACTIVE MOIETY