Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H28O3 |
| Molecular Weight | 328.4452 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 6 / 6 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
InChI
InChIKey=WKAVAGKRWFGIEA-DADBAOPHSA-N
InChI=1S/C21H28O3/c1-12(22)16-6-7-17-15-5-4-13-10-14(23)8-9-20(13,2)19(15)18(24)11-21(16,17)3/h10,15-17,19H,4-9,11H2,1-3H3/t15-,16+,17-,19+,20-,21+/m0/s1
| Molecular Formula | C21H28O3 |
| Molecular Weight | 328.4452 |
| 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 |
|---|---|---|
| Phylogenetic analysis of Bacillus P450 monooxygenases and evaluation of their activity towards steroids. | 2009-11 |
|
| Synthetic organic chemistry based on small ring compounds. | 2007-07 |
|
| Endogenous selective inhibitors of 11beta-hydroxysteroid dehydrogenase isoforms 1 and 2 of adrenal origin. | 2005-11-24 |
|
| Influence of substituents at C11 on hydroxylation of progesterone analogs by Bacillus sp. | 2002-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:33:18 GMT 2025
by
admin
on
Mon Mar 31 22:33:18 GMT 2025
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| Record UNII |
9Y1Y86O4T5
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID101031475
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516-15-4
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208-222-1
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m790
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admin on Mon Mar 31 22:33:18 GMT 2025 , Edited by admin on Mon Mar 31 22:33:18 GMT 2025
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PRIMARY | Merck Index | ||
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11-Ketoprogesterone
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admin on Mon Mar 31 22:33:18 GMT 2025 , Edited by admin on Mon Mar 31 22:33:18 GMT 2025
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9Y1Y86O4T5
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94166
Created by
admin on Mon Mar 31 22:33:18 GMT 2025 , Edited by admin on Mon Mar 31 22:33:18 GMT 2025
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