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ALLOPREGNENOLONE;5-ALPHA-PREGNA-16-ENE-3-BETA-OL-20-ONE
SpectraBase Compound ID 86qPMJzdm30
InChI InChI=1S/C21H32O2/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/h6,14-16,18-19,23H,4-5,7-12H2,1-3H3/t14-,15-,16-,18-,19-,20-,21+/m0/s1
InChIKey SFXPZLCQRZASKK-CKBUFISISA-N
Mol Weight 316.5 g/mol
Molecular Formula C21H32O2
Exact Mass 316.24023 g/mol
Enantiomer InChIKey SFXPZLCQRZASKK-VAOHTGRUSA-N
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Prof. Spiteller, University Bayreuth, Germany
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 © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N:D2O
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
  • ALLOPREGNENOLONE;5-ALPHA-PREGN-16-EN-3-BETA-OL-20-ONE
  • 3-BETA-HYDROXY-5-ALPHA-PREGN-16-ENE-3-BETA-OL-20-ONE
  • 5-ALPHA-PREGN-16-EN-3-BETA-OL-20-ONE
  • 3-Hydroxypregn-16-en-20-one
  • 3.BETA.-HYDROXY-5.ALPHA.-PREGN-16-ENE-20-ONE
  • 1-((3S,5S,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethanone
Title Journal or Book Year
Conversion of Tomato Saponins to Pregnane Derivatives Chemical and Pharmaceutical Bulletin 2014
A Pregnane Glycoside from Overripe Tomato Chemical and Pharmaceutical Bulletin 2008
Mechanism for Conversion of Spirosolane Derivative into Pregnane Chemical and Pharmaceutical Bulletin 2008
Efficient Conversion of Tomatidine into Neuritogenic Pregnane Derivative Chemical and Pharmaceutical Bulletin 2007

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