Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H28O3 |
| Molecular Weight | 304.4238 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@]12CC(=O)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@]34C)[C@@H]1CCC2=O
InChI
InChIKey=IUNYGQONJQTULL-UFTZPVOZSA-N
InChI=1S/C19H28O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h11-14,17,20H,3-10H2,1-2H3/t11-,12+,13-,14-,17+,18-,19-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Isotope ratio mass spectrometry analysis of the oxidation products of the main and minor metabolites of hydrocortisone and cortisone for antidoping controls. | 2009-03 |
|
| The effects of sex, age and commensal way of life on levels of fecal glucocorticoid metabolites in spiny mice (Acomys cahirinus). | 2008-09-03 |
|
| In vitro biosynthesis of novel 5beta-reduced steroids by the testis of the round goby, Neogobius melanostomus. | 2005-01-01 |
|
| Endogenous urinary steroids in premenopausal women with uterine leiomyomas. | 2004-01 |
|
| Glucocorticoid metabolites inhibit the metabolism of androstenedione in red blood cells of ruminants. | 2003-03 |
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26943-1
Created by
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1661-8
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34214-7
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15005-2
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34213-9
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26944-9
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6702-5
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40814-6
Created by
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34215-4
Created by
admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025
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| Code System | Code | Type | Description | ||
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11-Ketoandrosterone
Created by
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102029
Created by
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3T4E87JT27
Created by
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1231-82-9
Created by
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DTXSID901043038
Created by
admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025
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56412
Created by
admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025
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SUBSTANCE RECORD
