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Oxyresveratrol

Compound with spectra: 10 NMR, and 1 MS (GC)

Oxyresveratrol
SpectraBase Compound ID E2UPYzPaJOU
InChI InChI=1S/C14H12O4/c15-11-4-3-10(14(18)8-11)2-1-9-5-12(16)7-13(17)6-9/h1-8,15-18H/b2-1+
InChIKey PDHAOJSHSJQANO-OWOJBTEDSA-N
Mol Weight 244.25 g/mol
Molecular Formula C14H12O4
Exact Mass 244.073559 g/mol

View Spectrum of Oxyresveratrol

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.

View Spectrum of Oxyresveratrol

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.

View Spectrum of Oxyresveratrol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of Oxyresveratrol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of Oxyresveratrol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of Oxyresveratrol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of Oxyresveratrol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of Oxyresveratrol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum E1-39-3278-2
(E)-2,4',5-trihydroxystilbene
2-[(E)-2-(4-bromophenyl)ethenyl]benzene-1,4-diol
3-METHOXY-5-HYDROXY-4'-O-PRENYL-(CIS)-STILBENE
TRANS-3,3',5,5'-TETRAHYDROXY-4-METHOXY-STILBENE
GRAMISTILBENOID_A;(E)-5-(3,5-DIHYDROXYSTYRYL)-2-(2-HYDROXYETHYL)-BENZENE-1,3-DIOL
(E)-1-(3,5-Dimethoxyphenyl)-2-[4-(Octyloxy)phenyl]ethene
(E)-1-[4-(Dodecyloxy)phenyl]-2-(3,5-dimethoxyphenyl)ethene
(E)-1-[4-(Hexyloxy)phenyl]-2-(3,5-dimethoxyphenyl)ethene
Pterostilbene, mono-TMS
3,5-DIMETHOXY-4'-O-PRENIL-TRANS-STILBENE
Title Journal or Book Year
Constituents of the Bark and Twigs of Artocarpus dadah with Cyclooxygenase Inhibitory Activity Journal of Natural Products 2002
Stilbene and 2-Arylbenzofuran Glucosides from the Rhizomes of Schoenocaulon officinale. Chemical and Pharmaceutical Bulletin 2002
A New Dimeric Stilbene with Tyrosinase Inhibitiory Activity From Artocarpus gomezianus Journal of Natural Products 2001
A Novel Stilbene Glucoside, Oxyresveratrol 3′ -O-β-Glucopyranoside, from the Root Bark ofMorus alba Planta Medica 1996
Antifungal stress compounds from Veratrum grandiflorum leaves treated with cupric chloride Phytochemistry 1992
Two Phenolic Glycosides from the Root Bark of the Cultivated Mulberry Tree (Morus lhou) Journal of Natural Products 1986
Structures of Kuwanons Y and Z, Two New Stilbene Derivatives from the Cultivated Mulberry Tree (Morus alba L.) HETEROCYCLES 1986
Structures of Kuwanols A and B, Two Novel Stilbene Derivatives from the Cultivated Mulberry Tree (Morus bombycis Koidz.) HETEROCYCLES 1985

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