7-ALPHA-HYDROXY-ANDROST-4-EN-3,17-DIONE
Compound with spectra: 4 NMR, and 1 MS (GC)
| SpectraBase Compound ID | Ey34jcWO6mh |
|---|---|
| InChI | InChI=1S/C19H26O3/c1-18-7-5-12(20)9-11(18)10-15(21)17-13-3-4-16(22)19(13,2)8-6-14(17)18/h9,13-15,17,21H,3-8,10H2,1-2H3/t13-,14-,15+,17-,18-,19-/m0/s1 |
| InChIKey | LFWLQMQUJQUZBD-TYHLISGHSA-N |
| Mol Weight | 302.41 g/mol |
| Molecular Formula | C19H26O3 |
| Exact Mass | 302.188195 g/mol |
| Enantiomer InChIKey | LFWLQMQUJQUZBD-BENAYJGTSA-N |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Dr. Makin, London Hospital Medical College, UK |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| 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 | CDCl3 |
- 7-ALPHA-HYDROXY-ANDROST-4-ENE-3,17-DIONE
- ANDROST-4-ENE-3,17-DIONE-7-ALPHA-OL
- ANDROST-4-ENE-7.ALPHA.-OL-3,17-DIONE
- (7R,8R,9S,10R,13S,14S)-7-hydroxy-10,13-dimethyl-7,8,9,10,11,12,13,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17(2H,6H)-dione
- 7-HYDROXYANDROST-4-ENE-3,17-DIONE
3-BETA-[2-(TRIPHENYLSILYL)-ETHOXYCARBONYLOXY]-ANDROST-5-EN-17-ONE
Androst-5-en-17-one, 3-[(dimethylphosphinyl)oxy]-, (3.beta.)-
5-Androsten-3β-ol-17-one enanthate
heptanoic acid, 17-oxoandrost-5-en-3-yl ester
17-OXA-ANDROST-5-ENE-3-BETA-YL-HEXANOATE
17-OXA-ANDROST-5-ENE-3-BETA-YL-PENTANOATE
3-BETA-(D/L-1,2-DI-O-PALMITOYLGLYCERO)-THIO-ANDROST-5-EN-17-ONE
Dehydroepiandrosterone hemisuccinate
17-OXA-ANDROST-5-ENE-3-BETA-YL-BUTANOATE
| Title | Journal or Book | Year |
|---|---|---|
| An unusual ring—A opening and other reactions in steroid transformation by the thermophilic fungus Myceliophthora thermophila | The Journal of Steroid Biochemistry and Molecular Biology | 2009 |
| 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 |
| Microbial transformation of steroids: Contribution to 14α-hydroxylations | Steroids | 1995 |
| Microbial hydroxylation of steroids. 8. Incubation of Cn halo- and other substituted steroids with Cn hydroxylating fungi | Canadian Journal of Chemistry | 1982 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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