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
[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
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 |
---|---|---|
Cross talk between corticosteroids and alpha-adrenergic signalling augments cardiomyocyte hypertrophy: a possible role for SGK1. | 2006 Jun 1 |
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Local amplification of glucocorticoids by 11 beta-hydroxysteroid dehydrogenase type 1 promotes macrophage phagocytosis of apoptotic leukocytes. | 2006 Jun 15 |
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Resveratrol inhibits 11β-hydroxysteroid dehydrogenase type 1 activity in rat adipose microsomes. | 2013 Sep |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:01:49 GMT 2023
by
admin
on
Fri Dec 15 15:01:49 GMT 2023
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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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-
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Classification Tree | Code System | Code | ||
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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
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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
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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
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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
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Code System | Code | Type | Description | ||
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100000126063
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78600
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FO4V44A3G3
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C003552
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admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
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SUB32794
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admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
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9702
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admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
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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
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PRIMARY | Merck Index | ||
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DTXSID40861617
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admin on Fri Dec 15 15:01:49 GMT 2023 , Edited by admin on Fri Dec 15 15:01:49 GMT 2023
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5311364
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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
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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
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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
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PRIMARY |
Related Record | Type | Details | ||
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TARGET -> AGONIST |
Potent mineralocorticoid, with generally greater such activity than that of corticosterone.
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