7-O-GALACTOSIDE-ISOVITEXIN
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Name
7-O-GALACTOSIDE-ISOVITEXIN
IUPAC name
5-hydroxy-2-(4-hydroxyphenyl)-6-((2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-7-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one
SMILES
C1=CC(=CC=C1C3=CC(=O)C2=C(C(=C(C=C2O3)O[C@H]4[C@@H]([C@H]([C@H]([C@H](O4)CO)O)O)O)[C@H]5[C@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O)O
Molecular formula
C27H30O15
Molecular weight
594.52 g/mol
Monoisotopic mass
594.1585 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Silene latifolia Poir. | leaf | - |
Steyns, J.M., Vannigtevecht, G., Niemann, G.J., Brederode, J.V. (1983). Differential regulation of flavone glycosylation during ontogeny of Silene pratensis. Z Naturforsch Ser C, 38(7/8), 544-548 doi:10.1515/znc-1983-7-808
|
| Silene latifolia Poir. | seed | - |
Vanbrederode, J., Steyns, J.M. (1983). Ontogeny and biosynthesis of isovitexin 7-o-galactoside in a mutant of Silene pratensis unable to glycosylate this compound in the petals. Z Naturforsch Ser C, 38(7/8), 549-550 doi:10.1515/znc-1983-7-809
|