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
[H][C@@]12CC[C@H](C(C)=O)[C@@]1(C)CC(=O)[C@@]3([H])[C@@]2([H])CCC4=CC(=O)CC[C@]34C
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 |
---|---|---|
Endogenous selective inhibitors of 11beta-hydroxysteroid dehydrogenase isoforms 1 and 2 of adrenal origin. | 2005 Nov 24 |
|
Synthetic organic chemistry based on small ring compounds. | 2007 Jul |
|
Phylogenetic analysis of Bacillus P450 monooxygenases and evaluation of their activity towards steroids. | 2009 Nov |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:11:36 GMT 2023
by
admin
on
Sat Dec 16 09:11:36 GMT 2023
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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 Sat Dec 16 09:11:36 GMT 2023 , Edited by admin on Sat Dec 16 09:11:36 GMT 2023
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11-Ketoprogesterone
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admin on Sat Dec 16 09:11:36 GMT 2023 , Edited by admin on Sat Dec 16 09:11:36 GMT 2023
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9Y1Y86O4T5
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94166
Created by
admin on Sat Dec 16 09:11:36 GMT 2023 , Edited by admin on Sat Dec 16 09:11:36 GMT 2023
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