APIGENIN-C-RHAMNOSYL-GLUCOSIDE

Structure

2D structure of APIGENIN-C-RHAMNOSYL-GLUCOSIDE
2D structure
Drag to rotate, scroll to zoom
3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 9851181

Names and identifiers

Name

APIGENIN-C-RHAMNOSYL-GLUCOSIDE

Also reported as

ISORHOIFOLIN

IUPAC name

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

SMILES

C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=CC4=C(C(O)=C3)C(=O)C=C(O4)C3=CC=C(O)C=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O

General information

Molecular formula

C27H30O14

Molecular weight

578.52 g/mol

Monoisotopic mass

578.1636 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
Yes

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

Plants with the compound

Plant Plant part Amount Reference
Avena ludoviciana Durieu leaf -
Harborne, J.B., Hall, E. (1964). Plant polyphenols-xii. the occurrence of tricin and of glycoflavones in grasses. Phytochemistry, 3(3), 421-428
Onopordum acanthium L. subsp. acanthium flower -
Karl, C., Muller, G., Pedersen, P.A. (1976). Zur phytochemie der bluten von Onopordon acanthium L.(eselsdistel). Dtsch Apoth Ztg, 116, 57