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NEOTOKOROGENIN=(25S)-5-BETA-SPIROSTAN-1-BETA,2-BETA,3-ALPHA-TRIOL
SpectraBase Compound ID JOiSDLc2WI8
InChI InChI=1S/C27H44O5/c1-14-7-10-27(31-13-14)15(2)22-21(32-27)12-19-17-6-5-16-11-20(28)23(29)24(30)26(16,4)18(17)8-9-25(19,22)3/h14-24,28-30H,5-13H2,1-4H3/t14-,15+,16-,17-,18+,19+,20+,21+,22+,23-,24-,25+,26+,27-/m1/s1
InChIKey SRTGQBIWSBCVSM-RXWDRLOESA-N
Mol Weight 448.6 g/mol
Molecular Formula C27H44O5
Exact Mass 448.318875 g/mol
Enantiomer InChIKey SRTGQBIWSBCVSM-MFAMRLCHSA-N
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Chloroform-d
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
  • Neotokorogenin
  • Tokorogenin
Title Journal or Book Year
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
Protoyonogenin and protoneoyonogenin from the aerial parts and tissue cultures of Dioscorea tokoro Phytochemistry 1983
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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