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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

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

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

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:01:49 GMT 2023
Edited
by admin
on Fri Dec 15 15:01:49 GMT 2023
Record UNII
FO4V44A3G3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
DEHYDROCORTICOSTERON
WHO-DD  
Common Name English
11-DEHYDROCORTICOSTERONE [MI]
Common Name English
Classification Tree Code System Code
LOINC 82846-7
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
LOINC 82849-1
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
LOINC 82848-3
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
LOINC 82847-5
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
Code System Code Type Description
SMS_ID
100000126063
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
CHEBI
78600
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
FDA UNII
FO4V44A3G3
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
MESH
C003552
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
EVMPD
SUB32794
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
NSC
9702
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
MERCK INDEX
m4143
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID40861617
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
PUBCHEM
5311364
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
CAS
72-23-1
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-776-2
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
WIKIPEDIA
11-Dehydrocorticosterone
Created by admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Potent mineralocorticoid, with generally greater such activity than that of corticosterone.