6β-Hydroxyandrosterone
Compound with spectra: 3 NMR, 1 FTIR, 1 Raman, and 3 MS (GC)
| SpectraBase Compound ID | AJDh7dqxUdd |
|---|---|
| InChI | InChI=1S/C19H28O3/c1-18-7-5-11(20)9-15(18)16(21)10-12-13-3-4-17(22)19(13,2)8-6-14(12)18/h9,12-14,16-17,21-22H,3-8,10H2,1-2H3/t12-,13-,14-,16+,17-,18+,19-/m0/s1 |
| InChIKey | XSEGWEUVSZRCBC-ZVBLRVHNSA-N |
| Mol Weight | 304.43 g/mol |
| Molecular Formula | C19H28O3 |
| Exact Mass | 304.203845 g/mol |
| Enantiomer InChIKey | XSEGWEUVSZRCBC-JELAZNBBSA-N |
| Copyright | Copyright © 2014-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A5735-000 |
| Copyright | Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A5735-000 |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Prof. Spiteller, University Bayreuth, Germany |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Dr. Makin, London Hospital Medical College, UK |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | AH-135-1140-4 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|
| 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 |
- 4-Androsten-6β,17β-diol-3-one
- 6β-Hydroxytestosterone
- (6beta,17beta)-6,17-dihydroxyandrost-4-en-3-one
- 6.BETA.,17.BETA.-DIHYDROXY-ANDROST-4-ENE-3-ONE
- ANDROST-4-ENE-6.BETA.,17.BETA.-DIOL-3-ONE
- (6R,8R,9S,10R,13S,14S,17S)-6,17-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
- 6,17-DIHYDROXYANDROST-4-EN-3-ONE
Androst-4-ene-3,6,17-triol
6.beta.-Methylpregn-4-en-3-one
6-METHYLENE-ANDROST-4-ENE-17-BETA-OL-3-ONE
6-BETA-CHLORO-ANDROSTAN-4-ENE-3,17-DIONE
6β-bromoandrost-4-ene-3,17-dione
6α-bromoandrost-4-ene-3,17-dione
4-FLUORO-5-ANDROSTEN-17-BETA-OL-3-ONE
ANDROST-4-ENE-6.BETA.-OL-3-ONE(6.BETA.-TRIMETHYLSILYL ETHER)
ANDROST-4-ENE-6.BETA.-OL-3-ONE-TRIMETHYLSILYL ETHER
| Title | Journal or Book | Year |
|---|---|---|
| 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 |
| Metabolism of anabolic steroids in humans: Synthesis of 6β-hydroxy metabolites of 4-chloro-1,2-dehydro-17α-methyltestosterone, fluoxymesterone, and metandienone | Steroids | 1995 |