CHRYSOSPLENETIN
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 5281608
Name
CHRYSOSPLENETIN
IUPAC name
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6,7-trimethoxy-4H-chromen-4-one
SMILES
COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O
Molecular formula
C19H18O8
Molecular weight
374.35 g/mol
Monoisotopic mass
374.1002 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Artemisia annua L. | - | 350 ppm |
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
|
| Artemisia annua L. | cell culture | 650 ppm |
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
|
| Matricaria chamomilla L. | essential oil | - |
Mericli, A.H., Korkmaz, Y. (1992). Flavonoids of a Matricaria chamomilla var. recutica sample with no chamazulene in the volatile oil. Acta Pharm Turc, 34(3), 71-73
|
| Matricaria chamomilla L. | flower | - |
Exner, J., Reiching, J., Cole, T.C.H., Becker, H. (1981). Methylated flavonoid-aglycones from Matricariae Flos. Planta Med, 41, 198-200 doi:10.1055/s-2007-971700
|
| Matricaria chamomilla L. | flower | - |
Hansel, R., Rimpler, H., Walther, K. (1966). A lipophilic flavone from the chamomile (Matricaria chamomilla L.). Naturwissenschaften, 53(1), 19
|
| Matricaria chamomilla L. | flower | - |
Repcak, M., Svehlikova, V., Imrich, J., Pihlaja, K. (1999). Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) rauschert. Biochem Syst Ecol, 27(7), 727-732 doi:10.1016/s0305-1978(98)00124-0
|