7-O-(FERULYL-GLUCOSYL)-ISOVITEXIN
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Name
7-O-(FERULYL-GLUCOSYL)-ISOVITEXIN
IUPAC name
((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-((5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-7-yl)oxy)tetrahydro-2H-pyran-2-yl)methyl (E)-3-(4-hydroxyphenyl)acrylate
SMILES
C1=CC(=CC=C1C3=CC(=O)C2=C(C(=C(C=C2O3)O[C@@H]5[C@H]([C@@H]([C@H]([C@H](COC(\C(=C(\C4=CC=C(C=C4)O)[H])[H])=O)O5)O)O)O)[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)O)O
Molecular formula
C36H36O17
Molecular weight
740.67 g/mol
Monoisotopic mass
740.1953 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Silene latifolia Poir. | leaf | - |
Niemann, G.J. (1981). A new acylated c-glycoflavone glycoside from Silene pratensis leaves. Acta Bot Neerl, 30, 475-478 doi:10.1111/j.1438-8677.1981.tb01271.x
|