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XANTHORIN-8-O-BETA-D-GENTIOBIOSIDE-NONAACETATE;1,5-DIACETOXY-2-METHOXY-7-METHYL-4-[[2,3,4-TRI-O-ACETYL-6-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYR

Compound with spectra: 1 NMR

XANTHORIN-8-O-BETA-D-GENTIOBIOSIDE-NONAACETATE;1,5-DIACETOXY-2-METHOXY-7-METHYL-4-[[2,3,4-TRI-O-ACETYL-6-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYR
SpectraBase Compound ID JdfFZHe2PzT
InChI InChI=1S/C46H50O25/c1-17-12-27-33(28(13-17)61-19(3)48)37(57)34-29(14-30(58-11)38(62-20(4)49)35(34)36(27)56)69-46-44(68-26(10)55)42(66-24(8)53)40(64-22(6)51)32(71-46)16-60-45-43(67-25(9)54)41(65-23(7)52)39(63-21(5)50)31(70-45)15-59-18(2)47/h12-14,31-32,39-46H,15-16H2,1-11H3/t31-,32+,39-,40+,41+,42-,43-,44+,45-,46+/m1/s1
InChIKey PAKPEJIPDQSCGL-KQBDFYDSSA-N
Mol Weight 1002.9 g/mol
Molecular Formula C46H50O25
Exact Mass 1002.264117 g/mol
Enantiomer InChIKey PAKPEJIPDQSCGL-TZNXKRMBSA-N

View Spectrum of XANTHORIN-8-O-BETA-D-GENTIOBIOSIDE-NONAACETATE;1,5-DIACETOXY-2-METHOXY-7-METHYL-4-[[2,3,4-TRI-O-ACETYL-6-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYR

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Title Journal or Book Year
Pigments of Fungi. LXV. Tetrahydroanthraquinone and Anthraquinone Gentiobiosides from the Fungus Dermocybe splendida Australian Journal of Chemistry 2000
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