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2''-O-ALPHA-L-RHAMNOPYRANOSYLVITEXIN

Compound with spectra: 3 NMR

2''-O-ALPHA-L-RHAMNOPYRANOSYLVITEXIN
SpectraBase Compound ID 5hGlYCqTIB8
InChI InChI=1S/C27H30O14/c1-9-19(33)21(35)23(37)27(38-9)41-26-22(36)20(34)16(8-28)40-25(26)18-13(31)6-12(30)17-14(32)7-15(39-24(17)18)10-2-4-11(29)5-3-10/h2-7,9,16,19-23,25-31,33-37H,8H2,1H3/t9-,16+,19-,20+,21+,22-,23+,25-,26+,27-/m0/s1
InChIKey LYGPBZVKGHHTIE-HUBYJIGHSA-N
Mol Weight 578.52 g/mol
Molecular Formula C27H30O14
Exact Mass 578.163556 g/mol
Enantiomer InChIKey LYGPBZVKGHHTIE-QRIAMTHQSA-N

View Spectrum of 2''-O-ALPHA-L-RHAMNOPYRANOSYLVITEXIN

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

View Spectrum of 2''-O-ALPHA-L-RHAMNOPYRANOSYLVITEXIN

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

View Spectrum of 2''-O-ALPHA-L-RHAMNOPYRANOSYLVITEXIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • VITEXIN-2''-O-RHAMNOPYRANOSIDE
APIGENIN-8-C-BETA-D-(2''-O-ALPHA-L-RHAMNOSYL)-GLUCOPYRANOSIDE
Title Journal or Book Year
Three Adducts of Butenolide and Apigenin Glycoside from the Leaves of Machilus japonica Journal of Natural Products 2009
Flavonoid glycosides from Cotoneaster thymaefolia Phytochemistry 1994
Studies on physiologically active substances in citrus peel. Part VI. Structure and hypotensive effect of flavonoid glycosides in kinkan (Fortunella japonica) peelings. Agricultural and Biological Chemistry 1985
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