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STIGMASTEROL-3-O-BETA-GLUCOPYRANOSIDE
SpectraBase Compound ID 8gevHOpes0F
InChI InChI=1S/C35H58O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h8-10,20-22,24-33,36-39H,7,11-19H2,1-6H3/b9-8+/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1
InChIKey VWDLOXMZIGUBKM-AUGXRQBFSA-N
Mol Weight 574.8 g/mol
Molecular Formula C35H58O6
Exact Mass 574.42334 g/mol
Enantiomer InChIKey VWDLOXMZIGUBKM-OIEUPCSPSA-N
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.
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 Unknown
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 CD3OD
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 CD3OD:CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
  • VWDLOXMZIGUBKM-AUGXRQBFSA-N
  • STIGMASTEROL-3-O-BETA-D-GLUCOPYRANOSIDE
  • STIGMASTERYL-3-O-BETA-D-GLUCOPYRANOSIDE
  • STIGMASTEROL-3-O-BETA-D-GLUCOPYRANOSIDE;SC2-MAJOR
  • STIGMASTEROL-GLUCOSIDE;3-O-BETA-D-GLUCOPYRANOSYL-24-(R)-ETHYL-22E-DIHYDRO-CHOLESTEROL
  • STIGMASTEROL-3-O-BETA-D-GLUCOPYRANOSIDE;STIGMAST-5,(22E)-DIEN-3-BETA-D-GLUCOPYRANOSIDE
  • STIGMASTEROL-GLUCOSIDE
Title Journal or Book Year
Chemical constituents of Viburnum betulifolium Chemistry of Natural Compounds 2013
New Constituents from the Rhizomes of Egyptian Iris germanica L. Molecules 2012
Bioactive Metabolites from Spilanthes acmella Murr. Molecules 2009
Saponins and Sapogenins from Brachiaria decumbens Stapf Journal of the Brazilian Chemical Society 2002

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