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11α-Hydroxytestosterone

Compound with spectra: 2 NMR, 1 FTIR, 1 Raman, and 2 MS (GC)

11α-Hydroxytestosterone
SpectraBase Compound ID LXtAADwF8xR
InChI InChI=1S/C19H28O3/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/h9,13-17,21-22H,3-8,10H2,1-2H3/t13-,14-,15+,16-,17+,18-,19-/m0/s1
InChIKey YQDZGFAYWGWSJK-RUOITVIXSA-N
Mol Weight 304.43 g/mol
Molecular Formula C19H28O3
Exact Mass 304.203845 g/mol
Enantiomer InChIKey YQDZGFAYWGWSJK-ZXVGSPHGSA-N

View Spectrum of 11α-Hydroxytestosterone

ATR-IR Spectrum
Copyright Copyright © 2014-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A5737-000

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Raman Spectrum
Copyright Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A5737-000

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MS (GC) Spectrum
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Dr. Makin, London Hospital Medical College, UK

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MS (GC) Spectrum
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Prof. Spiteller, University Bayreuth, Germany

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 4-Androsten-11a,17b-diol-3-one
  • 11-ALPHA,17-BETA-DIHYDROXY-ANDROST-4-EN-3-ONE
  • 11.ALPHA.,17.BETA.-DIHYDROXY-ANDROST-4-ENE-3-ONE
  • ANDROST-4-ENE-11.ALPHA.,17.BETA.-DIOL-3-ONE
  • (8S,9S,10R,11R,13S,14S,17S)-11,17-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
  • 11,17-DIHYDROXYANDROST-4-EN-3-ONE
11.ALPHA.,17.BETA.-DIHYDROXY-ANDROST-4-ENE-3-ONE
11β-Hydroxytestosterone
11β-Hydroxytestosterone
11α-Hydroxytestosterone
cis-11β, 21-dihydroxypregna-4,17(20)-dien-3-one
(8S,9S,10R,13S,14S,17S)-17-[2-(3-Hydroxy-naphthalen-2-ylmethoxy)-acetyl]-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one
Chol-4-en-24-oic acid, 12-hydroxy-3-oxo-, methyl ester, (12.alpha.)-
10-Methyl-11-hydroxy-1,2,4,5-tetradehydroestran-3,17-dione
Pregn-4-ene-3,12,20-trione
6-BETA,11-ALPHA-DIHYDROXYANDROST-4-EN-3-ONE
Pregn-4-en-3-one, 20,21-[[(1,1-dimethylethyl)borylene]bis(oxy)]-, (20R)-
20-EPI-3-DEHYDROXY-3-OXO-5,6-DIHYDRO-4,5-DEHYDROVERAZINE;(20R,25S)-3-OXO-22,26-IMINOCHOLESTA-4,22(N)-DIENE
Pregn-4-ene-3,20-dione-18,18,18-D3
3α,11β,21,21-tetrahydroxy-5β-pregnan-20-one
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
10.1186/1752-153x-7-164 "" ""
11α-Hydroxytestosterone
11.ALPHA.,17.BETA.-DIHYDROXY-ANDROST-4-ENE-3-ONE
11β-Hydroxytestosterone
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