Testosterone
Compound with spectra: 10 NMR, 4 FTIR, 1 Raman, and 8 MS (GC)
| SpectraBase Compound ID | 94P1FLQ5KFm |
|---|---|
| InChI | InChI=1S/C19H28O2/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/h11,14-17,21H,3-10H2,1-2H3/t14-,15-,16-,17-,18-,19-/m0/s1 |
| InChIKey | MUMGGOZAMZWBJJ-DYKIIFRCSA-N |
| Mol Weight | 288.43 g/mol |
| Molecular Formula | C19H28O2 |
| Exact Mass | 288.20893 g/mol |
| Enantiomer InChIKey | MUMGGOZAMZWBJJ-MGYGNFHQSA-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 | A6950-000 |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Aldrich Chemical Company, Inc., Milwaukee, Wisconsin |
| Solvent | Chloroform-d; Reference=TMS Spectrometer= Varian CFT-20 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3:DIOXANE |
| 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. |
|---|
| 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 |
| 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 | 147656 |
| Solvent | CDCl3 & DMSO-d6 |
| Copyright | Copyright © 2009-2024 John Wiley & Sons, Inc. 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 | 147656 |
| Solvent | CDCl3 & DMSO-d6 |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A6950-000 |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Fluka Chemie AG, Buchs, Switzerland |
| Technique | KBr WAFER |
| Copyright | Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A6950-000 |
| Technique | KBr1 0.65mg |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | FLUKA CHEMIE AG, BUCHS, SWITZERLAND |
| Technique | KBr WAFER |
| Copyright | Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | DigiLab GmbH (C) 2024 |
| Technique | GC/MS |
| Copyright | Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | DigiLab GmbH (C) 2024 |
| Technique | GC/MS |
| Copyright | Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | DigiLab GmbH (C) 2024 |
| Technique | GC/MS |
| 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 © 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 | M. Laura Mascotti, et al. Steroids, 10.1016/j.steroids.2016.03.018 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | CAY-2023-426-0 |
| Catalog Number | <a href=https://www.caymanchem.com/product/ISO60154>ISO60154</a> |
- 4-Androsten-17beta-ol-3-one
- 17-BETA-HYDROXY-ANDROST-4-EN-3-ONE,(TESTOSTERON)
- TESTOSTERONE;17-BETA-HYDROXY-ANDROST-4-EN-3-ONE
- ANDROST-4-EN-3-ONE, 17B-HYDROXY-,
- MERTESTATE
- ANDROLIN
- TESLEN
- 17BETA-HYDROXYANDROST-4-EN-3-ONE
- ANDROST-4-EN-3-ONE, 17-HYDROXY-, (17beta)-
- 17-Hydroxyandrost-4-en-3-one
- 17.BETA.-HYDROXY-ANDROST-4-ENE-3-ONE
- ANDROST-4-ENE-17.BETA.-OL-3-ONE
- Androderm
- Testoderm
- (8R,9S,10R,13S,14S,17S)-17-Hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-\rdodecahydrocyclopenta[a]phenanthren-3-one
- (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
- (1S,2R,10R,11S,14S,15S)-14-hydroxy-2,15-dimethyltetracyclo[8.7.0.0(2,7).0(11,15)]heptadec-6-en-5-one
- TESTOVIRON
2,3,4-13C3-Testosterone
Testosterone
17-Hydroxyandrost-4-en-3-one
(8R,9S,10R,13S,14S,17S)-16,16,17-trideuterio-10,13-dimethyl-17-oxidanyl-1,2,6,7,8,9,11,12,14,15-decahydrocyclopenta[a]phenanthren-3-one
Testosterone
[16,16,17-Trideuterio]-17.alpha.-hydroxyandrost-4-en-3-one
17-Hydroxyandrost-4-en-3-one
Epitestosterone
(17-alpha)-17-Hydroxyandrost-4-en-3-one
3-METHYLENE-ANDROST-4-EN-17-BETA-OL
21-Hydroxypregn-4-en-3-one
17-METHYLANDROST-4-EN-3-ONE
Androst-4-en-3-one, 17-methyl-
17-ALPHA-CHLOROANDROST-4-EN-3-ONE
Pregn-4-en-3-one, 20-methyl-
21-Hydroxypregn-4-en-3-one, carbonate (2:1)
17.alpha.,19-dihydroxyandrost-4-en-3-one
17-BETA-HYDROXY-2-OXA-ANDROST-4-EN-3-ONE
13-(1',3'-Dioxolan-2'-yl)-3-oxo-16,17-seco-17-nor-androst-5-ene-16-nitrile
| 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 |
| Metabolism of anabolic steroids in humans: Synthesis of 6β-hydroxy metabolites of 4-chloro-1,2-dehydro-17α-methyltestosterone, fluoxymesterone, and metandienone | Steroids | 1995 |
| Microbial transformation of steroids: Contribution to 14α-hydroxylations | Steroids | 1995 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |
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