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6-DEOXYJACAREUBIN
SpectraBase Compound ID 8LzORXafOFK
InChI InChI=1S/C18H14O5/c1-18(2)7-6-9-12(23-18)8-13-14(15(9)20)16(21)10-4-3-5-11(19)17(10)22-13/h3-8,19-20H,1-2H3
InChIKey NHNIESSJWQBRJW-UHFFFAOYSA-N
Mol Weight 310.31 g/mol
Molecular Formula C18H14O5
Exact Mass 310.084124 g/mol
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
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 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 ACETONE-D6
  • 6-Desoxyjacareubin
Title Journal or Book Year
Chemical constituents from the fungus Ganoderma tropicum (Jungh.) Bres. and their cytotoxic activities African Journal of Microbiology Research 2013
Antioxidant Phenolic Compounds of Cassava (Manihot esculenta) from Hainan Molecules 2011
Pyranoxanthones fromCalophyllum Inophyllum Journal of the Chinese Chemical Society 2004
An antifungal γ-pyrone and xanthones with monoamine oxidase inhibitory activity from Hypericum brasiliense Phytochemistry 1994
Components of the Root Bark of Morus insignis Bur. 1. Structures of Four New Isoprenylated Xathones, Morusignins A, B, C, and D HETEROCYCLES 1990
Carbon-13 n.m.r. study of naturally occurring xanthones Organic Magnetic Resonance 1977

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