U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H28O4
Molecular Weight 344.4446
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 11-DEHYDROCORTICOSTERONE

SMILES

C[C@]12CC(=O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO

InChI

InChIKey=FUFLCEKSBBHCMO-KJQYFISQSA-N
InChI=1S/C21H28O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-16,19,22H,3-8,10-11H2,1-2H3/t14-,15-,16+,19+,20-,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H28O4
Molecular Weight 344.4446
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Resveratrol inhibits 11β-hydroxysteroid dehydrogenase type 1 activity in rat adipose microsomes.
2013-09
Local amplification of glucocorticoids by 11 beta-hydroxysteroid dehydrogenase type 1 promotes macrophage phagocytosis of apoptotic leukocytes.
2006-06-15
Cross talk between corticosteroids and alpha-adrenergic signalling augments cardiomyocyte hypertrophy: a possible role for SGK1.
2006-06-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 17:35:53 GMT 2025
Edited
by admin
on Mon Mar 31 17:35:53 GMT 2025
Record UNII
FO4V44A3G3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEHYDROCORTICOSTERON
WHO-DD  
Preferred Name English
11-DEHYDROCORTICOSTERONE
MI  
Common Name English
17-(1-KETO-2-HYDROXYETHYL)-.DELTA.4-ANDROSTEN-3,11-DIONE
Common Name English
.DELTA.4-PREGNEN-21-OL-3,11,20-TRIONE
Common Name English
DEHYDROCORTICOSTERONE
Common Name English
KENDALL'S COMPOUND A
Common Name English
NSC-9702
Code English
21-HYDROXYPREGN-4-ENE-3,11,20-TRIONE
Systematic Name English
Dehydrocorticosteron [WHO-DD]
Common Name English
11-DEHYDROCORTICOSTERONE [MI]
Common Name English
Classification Tree Code System Code
LOINC 82846-7
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
LOINC 82849-1
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
LOINC 82848-3
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
LOINC 82847-5
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
Code System Code Type Description
SMS_ID
100000126063
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
CHEBI
78600
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
FDA UNII
FO4V44A3G3
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
MESH
C003552
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
EVMPD
SUB32794
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
NSC
9702
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
MERCK INDEX
m4143
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID40861617
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
PUBCHEM
5311364
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
CAS
72-23-1
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-776-2
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
WIKIPEDIA
11-Dehydrocorticosterone
Created by admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Potent mineralocorticoid, with generally greater such activity than that of corticosterone.