GOSSYPETIN
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 5280647
Name
GOSSYPETIN
IUPAC name
2-(3,4-dihydroxyphenyl)-3,5,7,8-tetrahydroxy-4H-chromen-4-one
SMILES
C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O)O
Molecular formula
C15H10O8
Molecular weight
318.24 g/mol
Monoisotopic mass
318.0376 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Alcea rosea L. | leaf | - |
Matlawska, I. (1990). Investigation of flavonoid compounds of selected species from Malvaceae family. Herba Pol, 36(3), 65-69
|
| Althaea cannabina L. | leaf | - |
Matlawska, I. (1990). Investigation of flavonoid compounds of selected species from Malvaceae family. Herba Pol, 36(3), 65-69
|
| Lotus corniculatus L. | bud | - |
Jay, M., Deluca, V., Ibrahim, R. (1983). Meta-methylation of flavonol rings a(8-) and b(3'-) is catalysed by two distinct o-methyltransferases in Lotus cornicultaus. Z Naturforsch Ser C, 38(5/6), 416-417 doi:10.1515/znc-1983-5-614
|
| Lotus corniculatus L. | bud | - |
Jay, M., Ibrahim, R.K. (1986). Biosynthesis of 8-substituted flavonoils in relation to ontogeny of flower color in Lotus corniculatus. Biochem Physiol Pflanz, 181(3), 199-206 doi:10.1016/s0015-3796(86)80050-6
|
| Lotus corniculatus L. | flower | - |
Jay, M., Ibrahim, R.K. (1986). Biosynthesis of 8-substituted flavonoils in relation to ontogeny of flower color in Lotus corniculatus. Biochem Physiol Pflanz, 181(3), 199-206 doi:10.1016/s0015-3796(86)80050-6
|
| Lotus corniculatus L. | leaf | - |
Jay, M., Hasan, A., Voirin, B., Viricel, M.R. (1978). Flavonoids of Lotus corniculatus. Phytochemistry, 17, 827-829 doi:10.1016/s0031-9422(00)94254-7
|
| Primula vulgaris Huds. subsp. vulgaris | flower | - |
Harborne, J.B. (1968). Comparative biochemistry of the flavonoids-vii. Correlations between flavonoid pigmentation and systematics in the family Primulaceae. Phytochemistry, 7(8), 1215-1230
|