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PINORESINOL;(+/-)-2,6-BIS-(4'-HYDROXY-3'-METHOXY-PHENYL)-3,7-DIOXABICYCLO-[3.3.0]-OCTANE
SpectraBase Compound ID 3dDwceuFCtM
InChI InChI=1S/C20H22O6/c1-23-17-7-11(3-5-15(17)21)19-13-9-26-20(14(13)10-25-19)12-4-6-16(22)18(8-12)24-2/h3-8,13-14,19-22H,9-10H2,1-2H3/t13-,14-,19+,20+/m0/s1
InChIKey HGXBRUKMWQGOIE-AFHBHXEDSA-N
Mol Weight 358.39 g/mol
Molecular Formula C20H22O6
Exact Mass 358.141638 g/mol
Enantiomer InChIKey HGXBRUKMWQGOIE-NSMLZSOPSA-N
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum X2-54-1163-4
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CBD-19-13-1
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QA-45-776-11
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 CD3OD
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.
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 ACETONE-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • (+)-PINORESINOL;(1R*,2S*,5R*,6S*)-2-(3'-METHOXY-4'-HYDROXYPHENYL)-6-(3''-METHOXY-4''-HYDROXYPHENYL)-3,7-DIOXABICYCLO-[3.3.0]-OCTANE
  • (+)-Pinoresinol
  • Pinoresinol
Title Journal or Book Year
Chemical Constituents of the Root of Jasminum giraldii Molecules 2013
Constituintes químicos voláteis e não-voláteis de Cochlospermum vitifolium (Willdenow) Sprengel Química Nova 2005
Biotransformation of Pinoresinol Diglucoside to Mammalian Lignans by Human Intestinal Microflora, and Isolation of Enterococcus faecalis Strain PDG-1 Responsible for the Transformation of (+)-Pinoresinol to (+)-Lariciresinol Chemical and Pharmaceutical Bulletin 2003
Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger Phytochemistry 1993
Structure of Novel Antioxidative Lignan Triglucoside Isolated from Sesame Seed HETEROCYCLES 1993
Phenolic lignans from flower buds of Magnolia fargesii Phytochemistry 1992
Synthesis of biologically active tetrahydro-furofuranlignan-(syringin, pinoresinol)- mono- and bis-glucosides Phytochemistry 1991
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