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NEVADENSIN;5,7-DIHYDROXY-6,8,4'-TRIMETHOXYFLAVONE
SpectraBase Compound ID 7Zpsy5zL0Qd
InChI InChI=1S/C18H16O7/c1-22-10-6-4-9(5-7-10)12-8-11(19)13-14(20)17(23-2)15(21)18(24-3)16(13)25-12/h4-8,20-21H,1-3H3
InChIKey KRFBMPVGAYGGJE-UHFFFAOYSA-N
Mol Weight 344.32 g/mol
Molecular Formula C18H16O7
Exact Mass 344.089603 g/mol
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CD-327-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Y4-80-99-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Y1-38-1009-0
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 DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
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 DMSO-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 CDCl3
  • 5,7-DIHYDROXY-6,8,4'-TRIMETHOXYFLAVONE
  • NEBADENSIN
  • NEVADENSIN
  • NEVANDENSIN-A
  • NEVADENSIN;5,4-DIHYDROXY-6,8,4'-TRIMETHOXYFLAVONE
  • 4H-1-benzopyran-4-one, 5,7-dihydroxy-6,8-dimethoxy-2-(4-methoxyphenyl)-
Title Journal or Book Year
A distinctive flavonoid chemistry for the anomalous genus Biebersteinia Phytochemistry 2001
Distribution of 8-oxygenated leaf-surface flavones in the genus Ocimum Phytochemistry 2001
A New Flavonol from Murraya paniculata var. omphalocarpa: 13C-NMR as a Useful Tool for Structure Elucidation of Polyoxyflavones HETEROCYCLES 1999
Phenylpropanoids and flavonoid glycosides from Lysionotus pauciflorus Phytochemistry 1998
13C NMR spectral assignment of the A-ring of polyoxygenated flavones Phytochemistry 1998
Nevadensin glycosides from Lysionotus pauciflorus Phytochemistry 1996
Highly oxygenated bioactive flavones from Tamarix Phytochemistry 1994

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