ISOSCOPARIN

Structure

2D structure of ISOSCOPARIN
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 442611

Names and identifiers

Name

ISOSCOPARIN

Also reported as

LUTEOLIN-3'-O-METHYL-6-C-BETA-D-GLUCOPYRANOSIDE

IUPAC name

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

SMILES

COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)O)[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O

General information

Molecular formula

C22H22O11

Molecular weight

462.41 g/mol

Monoisotopic mass

462.1162 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
No

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

Plants with the compound

Plant Plant part Amount Reference
Arrhenatherum elatius (L.) P.Beauv. ex J.Presl & C.Presl subsp. elatius leaf -
Jay, M., Ismaili, A. (1989). Flavones and c-glycosylflavones from the leaves of some Arrhenatherum species. Phytochemistry, 28(11), 3035-3037 doi:10.1016/0031-9422(89)80274-2
Barbarea vulgaris W.T.Aiton aerial parts -
Senatore, F., D'agostino, M., Dini, I. (2000). Flavonoid glycosides of Barbarea vulgaris L. (Brassicaceae). J Agr Food Chem, 48(7), 2659-2662 doi:10.1021/jf990625k
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
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