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1,4,8-TRIHYDROXYNAPHTHALENE-1-O-BETA-D-[6'-O-(3'',4'',5''-TRIHYDROXYBENZOYL)]-GLUCOPYRANOSIDE

Compound with spectra: 2 NMR

1,4,8-TRIHYDROXYNAPHTHALENE-1-O-BETA-D-[6'-O-(3'',4'',5''-TRIHYDROXYBENZOYL)]-GLUCOPYRANOSIDE
SpectraBase Compound ID 2eRc9Z9WC0P
InChI InChI=1S/C23H22O12/c24-11-4-5-15(17-10(11)2-1-3-12(17)25)34-23-21(31)20(30)19(29)16(35-23)8-33-22(32)9-6-13(26)18(28)14(27)7-9/h1-7,16,19-21,23-31H,8H2/t16-,19-,20+,21-,23-/m1/s1
InChIKey YDWMVKUZYROZHA-JTLUYSSBSA-N
Mol Weight 490.42 g/mol
Molecular Formula C23H22O12
Exact Mass 490.111126 g/mol
Enantiomer InChIKey YDWMVKUZYROZHA-QRDGOAKLSA-N

View Spectrum of 1,4,8-TRIHYDROXYNAPHTHALENE-1-O-BETA-D-[6'-O-(3'',4'',5''-TRIHYDROXYBENZOYL)]-GLUCOPYRANOSIDE

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

View Spectrum of 1,4,8-TRIHYDROXYNAPHTHALENE-1-O-BETA-D-[6'-O-(3'',4'',5''-TRIHYDROXYBENZOYL)]-GLUCOPYRANOSIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 1,4,8-TRIHYDROXYNAPHTHALENYL-1-O-BETA-D-[6'-0-[3''4'',5''-TRIHYDROXYBENZOYL)]-GLUCOPYRANOSIDE
1,4,8-TRIHYDROXYNAPHTHALENE-1-O-BETA-D-GLUCOPYRANOSYL-(1->6)-ALPHA-L-ARABINOPYRANOSIDE
1,4,8-TRIHYDROXYNAPHTHALENE-1-O-D-GLUCOPYRANOSYL-(1->6)-BETA-D-XYLOPYRANOSIDE
1,4,8-TRIHYDROXYNAPHTHALENE-1-O-[ALPHA-L-ARABINOFURANOSYL-(1->6)-BETA-D-GLUCOPYRANOSIDE]
4-O-{6-O-[4-O-(6-O-SYRINGYLOYL-BETA-D-GLUCOPYRANOSYL)-VANILLOYL]-BETA-D-GLUCOPYRANOSYL}-2-METHOXY-PARA-HYDROXYQUINONE
ACANTHOSIDE-C
EHLETIANOL_A;2-METHOXYHYDOQUINONE-1-O-(6-VANILLOYL)-BETA-D-GLUCOPYRANOSIDO-4-O-(6-SYRINGOYL)-BETA-D-GLUCOPYRANOSIDE
2-(6-BENZOYL-BETA-GLUCOPYRANOSYLOXY)-7-[2-[(2-OXO-2-PHENYL)-ETHYL]-BENZOYL]-5-HYDROXYBENZYL_ALCOHOL
3-HYDROXYPHLORETIN-4'-O-(4'',6''-DI-O-GALLOYL)-BETA-D-GLUCOPYRANOSIDE
GLEHLINOSIDE-A;(-)-SECO-ISOLARICIRESINOL-4-O-BETA-D-(6-O-VANILLOYL)-GLUCOPYRANOSIDE
QKFFBJAAEFVEBF-ZMXIUBSNSA-N
Title Journal or Book Year
Studies on Cytotoxic Activity against HepG-2 Cells of Naphthoquinones from Green Walnut Husks of Juglans mandshurica Maxim Molecules 2015
New Naphthalenyl Glucosides from the Roots of Juglans mandshurica Journal of Natural Products 1996
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