3α,11β-dihydroxy-5α-androstan-17-one
Compound with spectra: 3 NMR, 1 FTIR, and 2 MS (GC)
| SpectraBase Compound ID | 4SMibO1TBN7 |
|---|---|
| InChI | InChI=1S/C19H30O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h11-15,17,20-21H,3-10H2,1-2H3/t11-,12+,13-,14-,15-,17+,18-,19-/m0/s1 |
| InChIKey | PIXFHVWJOVNKQK-PTXZMSDUSA-N |
| Mol Weight | 306.45 g/mol |
| Molecular Formula | C19H30O3 |
| Exact Mass | 306.219495 g/mol |
| Enantiomer InChIKey | PIXFHVWJOVNKQK-RWTSLDOESA-N |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A1330-000 |
| 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 © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Sigma-Aldrich Co. LLC. |
| Source of Spectrum | Sigma-Aldrich Co. LLC. |
| Catalog Number | 286117 |
| Solvent | CDCl3 |
| Copyright | Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Sigma-Aldrich Co. LLC. |
| Source of Spectrum | Sigma-Aldrich Co. LLC. |
| Catalog Number | 286117 |
| Solvent | CDCl3 |
- 11beta-Hydroxyandrosterone
- 3,11-Dihydroxyandrostan-17-one
- 5.ALPHA.-ANDROSTANE-3.ALPHA.,11.BETA.-DIOL-17-ONE
- (3R,5S,8S,9S,10S,11S,13S,14S)-3,11-dihydroxy-10,13-dimethyltetradecahydro-1H-cyclopenta[a]phenanthren-17(2H)-one
3α,11α-dihydroxy-5β-androstan-17-one
5β-Androstane-3α,11β-diol-17-one
3,11-Dihydroxyandrostan-17-one
5β-Androstane-3α,11β-diol-17-one
11-Hydroxyandrosterone
5α-Androstan-3β,11β-diol-17-one
5α-Androstan-3α,11β-diol-17-one
3,11-Dihydroxyandrostan-17-one
3,11-Dihydroxyandrostan-17-one
3,11-Dihydroxyandrostan-17-one
3β,11β-dihydroxy-5α-androstan-17-one
D-Homo-androstan-11a-ol-2,17a-dione
2,17A-DIKETO-(11-ALPHA)-HYDROXY-D-HOMOANDROSTAN
3α,11β,21,21-tetrahydroxy-5β-pregnan-20-one
Cholestane-3,11-diol
3-ALPHA,11-BETA-DIHYDROXY-17A-OXA-D-HOMO-5-ALPHA-ANDROSTAN-17-ONE
5β-pregnane-3α,11β,20α,21-tetrol
(17-formyloxy-11-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl) formate
Androstane-3,11,17-triol, 3,17-diformate, (3.alpha.,5.beta.,11.beta.,17.beta.)-
| Title | Journal or Book | Year |
|---|---|---|
| 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 |