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Epipregnanolone
SpectraBase Compound ID 5YNtvXOVrGt
InChI InChI=1S/C21H34O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h14-19,23H,4-12H2,1-3H3/t14-,15+,16+,17-,18+,19+,20+,21-/m1/s1
InChIKey AURFZBICLPNKBZ-GRWISUQFSA-N
Mol Weight 318.5 g/mol
Molecular Formula C21H34O2
Exact Mass 318.25588 g/mol
Enantiomer InChIKey AURFZBICLPNKBZ-YJQDOJAJSA-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 P8180-000
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number P8180-000
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample M. L. LEWBART, CROZER-CHESTER MEDICAL CENTER, CHESTER, PENNSYLVANIA
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 P8180-000
Technique KBr1 0.68mg
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
  • 3b-Hydroxy-5b-pregnan-20-one
  • 5b-Pregnan-3b-ol-20-one
  • 3b-Hydroxy-5b-tetrahydroprogesterone
  • 3-BETA-HYDROXY-5-BETA-PREGNANE-20-ONE
  • 5B-PREGNAN-20-ONE, 3B-HYDROXY-,
Title Journal or Book Year
Microbial transformation of steroids: Contribution to 14α-hydroxylations Steroids 1995
Studies on the conformations in solution of 5β-steroids having different side chains by13C NMR spectroscopy Magnetic Resonance in Chemistry 1986

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