CORNICULATUSIN
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 5280695
Name
CORNICULATUSIN
Also reported as
GOSSYPETIN-8-METHYL ETHER; QUERCETIN-8-METHOXY
IUPAC name
2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-8-methoxy-4H-chromen-4-one
SMILES
COC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O)O
Molecular formula
C16H12O8
Molecular weight
332.26 g/mol
Monoisotopic mass
332.0532 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Lotus corniculatus L. | flower | - |
Harborne, J.B., Saleh, N.A.M., Smith, D.M. (1978). On the natural occurrence of gossypetin 7- and 8-monoethyl ethers. Phytochemistry, 17, 589-591 doi:10.1016/s0031-9422(00)89389-9
|
| Lotus corniculatus L. | flower | - |
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
|
| 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
|
| Petrosedum thartii (L.P.Hébert) Niederle | leaf | - |
Niemann, G.J., Visser-simons, J.M.J., 'thart, H. (1976). Flavonoids of some species of Sedum. Planta Med, 30, 384 doi:10.1055/s-0028-1097748
|
| Petrosedum thartii (L.P.Hébert) Niederle | leaf | - |
Stevens, J.F., Hart, H., Elema, E.T., Bolck, A. (1996). Flavonoid variation in eurasian Sedum and Sempervivum. Phytochemistry, 41(2), 503-512 doi:10.1016/0031-9422(95)00573-0
|