17β-Dihydroandrosterone
Compound with spectra: 3 NMR, 2 FTIR, 1 Raman, and 4 MS (GC)
| SpectraBase Compound ID | GjO4PHTUOr8 |
|---|---|
| InChI | InChI=1S/C19H32O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-17,20-21H,3-11H2,1-2H3/t12-,13+,14-,15-,16-,17-,18-,19-/m0/s1 |
| InChIKey | CBMYJHIOYJEBSB-KHOSGYARSA-N |
| Mol Weight | 292.5 g/mol |
| Molecular Formula | C19H32O2 |
| Exact Mass | 292.24023 g/mol |
| Enantiomer InChIKey | CBMYJHIOYJEBSB-LPACOWDJSA-N |
| Copyright | Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A1170-000 |
| Copyright | Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A1170-000 |
| Copyright | Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A1170-000 |
| Technique | KBr1 0.47mg |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Dr. Makin, London Hospital Medical College, UK |
| 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 | Prof. D. Henneberg, MPI f. Kohlenforschung, Muelheim a.d.R., Germany |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | SWG-33-2105-0 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | PYRIDINE-D5 |
| 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 |
- 5α-Androstan-3α,17β-diol
- 3.alpha.,17.beta.-dihydroxy-5.alpha.-androstane
- Androstane-3,17-diol
- ANDROSTANE-3,17-DIOL, (3alpha,5alpha,17beta)-
- 5a-Androstane-3a,17b-diol
- (3R,5S,8R,9S,10S,13S,14S,17S)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol
- (1S,2S,5R,7S,10R,11S,14S,15S)-2,15-dimethyltetracyclo[8.7.0.0(2,7).0(11,15)]heptadecane-5,14-diol
5b-Androstane-3b,17b-diol
5-ALPHA-ANDROSTAN-3-ALPHA,17-ALPHA-DIOL
5a-Androstane-3a,17b-diol
5β-Androstan-3β,17β-diol
5b-Androstane-3a,17b-diol
17β-Dihydroepiandrosterone
5-ALPHA-ANDROSTAN-3-BETA,17-ALPHA-DIOL
Androstane-3,17-diol
Androstane-3,17-diol
5β-Androstan-3α,17β-diol
Androstane-3,17-diol
3.ALPHA.,17.BETA.-DIHYDROXY-5.ALPHA.-ANDROSTAN
(3-BETA,17A-BETA)-DIHYDROXY-D-HOMOANDROSTAN
D-Homo-androstane-3b,17ab-diol
3.beta.-Hydroxy-17.beta.-methyl-5a-androstane
3-ALPHA-AZIDO-PREGNANE
3-BETA-AZIDO-PREGNANE
5.alpha.-Pregnan-3.beta.-amine, N,N-dimethyl-
5.beta.-androst-16-en-3.alpha.-ol
5.beta.-androstane-3.alpha.-ol-trimethylsilyl ether
3B-TRIMETHYLSILOXY-5A-ANDROSTANE
(2-BETA,17A-BETA)-DIHYDROXY-D-HOMOANDROSTAN
| Title | Journal or Book | Year |
|---|---|---|
| Transformation of a series of saturated isomeric steroidal diols by Aspergillus tamarii KITA reveals a precise stereochemical requirement for entrance into the lactonization pathway | The Journal of Steroid Biochemistry and Molecular Biology | 2010 |
| Transformation of some 3α-substituted steroids by Aspergillus tamarii KITA reveals stereochemical restriction of steroid binding orientation in the minor hydroxylation pathway | The Journal of Steroid Biochemistry and Molecular Biology | 2010 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |