Secondary Metabolites Search

2''-O-RHAMNOSYL-ISOVITEXIN

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Structure

2D structure of 2''-O-RHAMNOSYL-ISOVITEXIN
2D structure
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3D model

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

Names and identifiers

Name

2''-O-RHAMNOSYL-ISOVITEXIN

IUPAC name

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

SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@H]2[C@@H]([C@H]([C@@H](O[C@@H]2C3=C(C=C4C(=C3O)C(=O)C=C(O4)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O

General information

Molecular formula

C27H30O14

Molecular weight

578.52 g/mol

Monoisotopic mass

578.1636 Da

Classification

Pathway:
Shikimates and Phenylpropanoids
Superclass:
Flavonoids
Class:
Flavones
Glycoside:
Yes

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

Plants with the compound

Plant Plant part Amount Reference
Crataegus monogyna Jacq. flower -
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
Silene latifolia Poir. - -
Mastenbroek, O., Vanbrederode, J. (1986). The possible evolution of Silene pratensis as deduced from present day variation patterns. Biochem Syst Ecol, 14(2), 165-181 doi:10.1016/0305-1978(86)90058-x
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