KAEMPFEROL-3-O-GLUCOSIDE-7-O-RHAMNOSIDE

Structure

2D structure of KAEMPFEROL-3-O-GLUCOSIDE-7-O-RHAMNOSIDE
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 44258812

Names and identifiers

Name

KAEMPFEROL-3-O-GLUCOSIDE-7-O-RHAMNOSIDE

IUPAC name

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

SMILES

CC1[C@@H]([C@@H](C([C@@H](O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O[C@H]4C(C([C@@H](C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O

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
Equisetum telmateia Ehrh. seedling -
Beckert, C., Veit, M., Geiger, H., Czygan, F.C. (1993). Flavonoids of Equisetum sylvaticum, Equisetum pratense, and Equisetum x bowmanii. Planta Med Suppl, 59, A696-A697 doi:10.1055/s-2006-959988
Lotus tenuis Waldst. & Kit. ex Willd. - -
Wagner, M.L., Strittmatter, C.D., Kade, M., Rivero, M., Ricco, R.A., Gurni, A.A. (1996). Phytochemical survey of Lotus tenuis Waldst. and Kit. Phyton(Buenos Aires), 58(1/2), 141-146