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DIOSGENIN=(25R)-5-SPIROSTEN-3-BETA-OL
SpectraBase Compound ID 5hupG39HIZo
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+/m0/s1
InChIKey WQLVFSAGQJTQCK-CAKNJAFZSA-N
Mol Weight 414.6 g/mol
Molecular Formula C27H42O3
Exact Mass 414.313395 g/mol
Enantiomer InChIKey WQLVFSAGQJTQCK-MMUVMXEBSA-N
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
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
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 Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
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 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 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 CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • DIOSGENIN=(25R)-SPIROST-5-EN-3-BETA-OL
  • (25R)-SPIROST-5-EN-3-BETA-OL,(DIOSGENIN)
  • Diosgenin
Title Journal or Book Year
Steroidal prosapogenins from Dioscorea olfersiana Phytochemistry 1994
Carbon-13 NMR spectroscopy of steroidal sapogenins and steroidal saponins Phytochemistry 1985
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
Studies on the constituents of Aspidistra elatior Blume. I. On the steroids of the underground part. Chemical and Pharmaceutical Bulletin 1982
Spirostanic diosgenin precursors from Dioscorea composita tubers Phytochemistry 1982
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
Carbon-13 nmr spectra of 5β-steroidal sapogenins. Reassignment of the F-ring carbon signals of (25)-spirostans Tetrahedron Letters 1981
The Synthesis of (25R)-22αN-[15ξ,17α-2H2]-Spirosol-5-en-3β-ol ([15ξ,17α-2H2] Solasodine) and Assignment of the 13C N.M.R. Spectra of Solasodine and its Derivatives Australian Journal of Chemistry 1979
13C n.m.r. spectra of steroids —a survey and commentary Organic Magnetic Resonance 1977

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