ISOVITEXIN 7-O-GLUCOSIDE

Structure

2D structure of ISOVITEXIN 7-O-GLUCOSIDE
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js.

Names and identifiers

Name

ISOVITEXIN 7-O-GLUCOSIDE

Also reported as

ISOVITEXIN-7-GLUCOSIDE

IUPAC name

5-hydroxy-2-(4-hydroxyphenyl)-6-((2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

SMILES

OC[C@H]5O[C@@H](OC3=C([C@H]1O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1O)C(=C2C(=O)C=C(OC2=C3)C4=CC=C(O)C=C4)O)[C@H](O)[C@@H](O)[C@@H]5O

General information

Molecular formula

C27H30O15

Molecular weight

594.52 g/mol

Monoisotopic mass

594.1585 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
Yes

Chemical classification: NPClassifier (Kim et al., 2021)

Plants with the compound

Plant Plant part Amount Reference
Cerastium arvense L. subsp. suffruticosum (L.) Ces. flower -
Dubois, M.A., Zoll, A., Chopin, J. (1985). Isomollupentin-o-glucosides from Cerastium arvense. Phytochemistry, 24(5), 1077-1080 doi:10.1016/s0031-9422(00)83186-6
Dipsacus fullonum L. - -
List, P.H. and Horhammer, L., Hager's Handbuch der Pharmazeutischen Praxis, Vols. 2-6, Springer-Verlag, Berlin, 1969-1979.
Silene latifolia Poir. flower -
Mastenbroek, O., Knorr, J.J., Kamps-heinsbroek, R., Maas, J.W., Steyns, J.M., Vanbrederode, J. (1983). The flavones of the european species of Silene section elisanthe. Z Naturforsch Ser C, 38(11/12), 894-898 doi:10.1515/znc-1983-11-1202