6-BETA,11-ALPHA-DIHYDROXYPROGESTERONE
Compound with spectra: 3 NMR, and 1 MS (GC)
| SpectraBase Compound ID | FyZyZYUnohM |
|---|---|
| InChI | InChI=1S/C21H30O4/c1-11(22)14-4-5-15-13-9-17(24)16-8-12(23)6-7-20(16,2)19(13)18(25)10-21(14,15)3/h8,13-15,17-19,24-25H,4-7,9-10H2,1-3H3/t13-,14+,15-,17+,18+,19+,20-,21+/m0/s1 |
| InChIKey | KDHBHXVDYRGRDL-KDZLLLCRSA-N |
| Mol Weight | 346.47 g/mol |
| Molecular Formula | C21H30O4 |
| Exact Mass | 346.214409 g/mol |
| Enantiomer InChIKey | KDHBHXVDYRGRDL-XFLXTARGSA-N |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Prof. Spiteller, University Bayreuth, Germany |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C5D5N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C5D5N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
- 6.BETA.,11.ALPHA.-DIHYDROXY-PREGN-4-ENE-3,20-DIONE
- (6R,8S,9S,10R,11R,13S,14S,17S)-17-acetyl-6,11-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
- 6,11-DIHYDROXYPREGN-4-ENE-3,20-DIONE
6-BETA,11-ALPHA-DIHYDROXY-ANDROST-4-EN-3,17-DIONE
Androst-4-ene-3,17-dione, 6-fluoro-11-hydroxy-, (6.beta.,11.alpha.)-
11β,21-dihydroxypregn-4-ene-3,20-dione, 21-carbonate (2:1)
Corticosterone, mono-TMS
Corticosterone 21-acetate
11.beta.-Hydroxy-20-phenylpregn-4,20-dien-3-one
Androst-4-ene-3,17-dione, 6-chloro-11-hydroxy-, (6.beta.,11.alpha.)-
3β,11β-dihydroxypregn-5-en-20-one, 3-acetate
3-BETA,11-ALPHA,16-BETA-TRIHYDROXYPREGN-5-EN-20-ONE
11β,20α-dihydroxy-3-oxopregn-4-en-21-oic acid, methyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Biotransformation of progesterone by Absidia griseolla var. igachii and Rhizomucor pusillus | Steroids | 2012 |
| Predominant allylic hydroxylation at carbons 6 and 7 of 4 and 5-ene functionalized steroids by the thermophilic fungus Rhizomucor tauricus IMI23312 | The Journal of Steroid Biochemistry and Molecular Biology | 2008 |
| Hydroxylation of progesterone by Cephalosporium aphidicola | Phytochemistry | 1994 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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