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Diosgenin
SpectraBase Compound ID G2zkZ6c4eBa
InChI InChI=1S/C27H42O3/c1-16-7-12-27(29-15-16)17(2)24-23(30-27)14-22-20-6-5-18-13-19(28)8-10-25(18,3)21(20)9-11-26(22,24)4/h5,16-17,19-24,28H,6-15H2,1-4H3/t16-,17+,19+,20-,21+,22+,23+,24+,25+,26+,27-/m1/s1
InChIKey WQLVFSAGQJTQCK-VKROHFNGSA-N
Mol Weight 414.6 g/mol
Molecular Formula C27H42O3
Exact Mass 414.313395 g/mol
Enantiomer InChIKey WQLVFSAGQJTQCK-QITUHIDSSA-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 S1600-000
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample M. L. Lewbart, Crozer-Chester Medical Center Chester, Pennsylvania
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian CFT-20
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. 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 PYRIDINE-D5
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 PYRIDINE-D5
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 © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number S1600-000
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 S1600-000
Technique KBr1 0.86mg
  • 5,20α,22α 25D-Spirosten-3β-ol
  • 3β-Hydroxy-5-spirostene
  • YAMOGENIN=(25S)-5-SPIROSTEN-3-BETA-OL
  • DIOSGENIN;REFERENCE-2
  • YAMOGENIN=(25S)-SPIROST-5-EN-3-BETA-OL
  • Yamogenin
  • SPIROST-5-EN-3B-OL, /25R/-,
Title Journal or Book Year
Chemical Constituents from <I>Solanum lyratum</I> Chinese Journal of Natural Medicines 2009
Microbial metabolism of methyl protodioscin by Aspergillus niger culture—A new androstenedione producing way from steroid The Journal of Steroid Biochemistry and Molecular Biology 2006
Biosynthesis of (25S)- and (25R)-furostanol glycosides from [1,2-13C2] acetate in Dioscorea tokoro tissue cultures Journal of the Chemical Society, Perkin Transactions 1 1984
Spirostanic diosgenin precursors from Dioscorea composita tubers Phytochemistry 1982
Carbon-13 nmr spectra of 5β-steroidal sapogenins. Reassignment of the F-ring carbon signals of (25)-spirostans Tetrahedron Letters 1981
Biosynthesis of yamogenin, neotokorogenin, and their (25R)-isomers from [1,2-13C2]acetate in Dioscorea tokoro tissue cultures Journal of the Chemical Society, Chemical Communications 1981

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