APIGENIN-2''-7-DI-O-GLUCOSYL-6-C-GLUCOSIDE

Structure

2D structure of APIGENIN-2''-7-DI-O-GLUCOSYL-6-C-GLUCOSIDE
2D structure
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3D model

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

Names and identifiers

Name

APIGENIN-2''-7-DI-O-GLUCOSYL-6-C-GLUCOSIDE

IUPAC name

6-((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)-5-hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,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](CO)O4)O)O)O)[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@@H]6[C@@H](O)[C@@H]([C@H]([C@H](CO)O6)O)O)O)O

General information

Molecular formula

C33H40O20

Molecular weight

756.66 g/mol

Monoisotopic mass

756.2113 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. - -
Dubois, (1981). Contribution to a study of c-glycoflavonoids in the Caryophyllaceae, in particular in Cerastium arvense L. Bull Trav Soc Pharm(Lyon), 25(1/4), 46-49