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
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
| 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
| Title | Date | PubMed |
|---|---|---|
| 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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:35:53 GMT 2025
by
admin
on
Mon Mar 31 17:35:53 GMT 2025
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| Record UNII |
FO4V44A3G3
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
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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
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LOINC |
82849-1
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admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
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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
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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
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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100000126063
Created by
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78600
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FO4V44A3G3
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admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
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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
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PRIMARY | |||
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SUB32794
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admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
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9702
Created by
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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
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PRIMARY | Merck Index | ||
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DTXSID40861617
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admin on Mon Mar 31 17:35:53 GMT 2025 , Edited by admin on Mon Mar 31 17:35:53 GMT 2025
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PRIMARY | |||
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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
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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
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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
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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
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
TARGET -> AGONIST |
Potent mineralocorticoid, with generally greater such activity than that of corticosterone.
|