Luteolin inhibits invasion of prostate cancer PC3 cells through E ...
Luteolin kháng PC3
From Wikipedia, the free encyclopedia
| Names | |
|---|---|
| IUPAC name
2-(3,4-Dihydroxyphenyl)- 5,7-dihydroxy-4-chromenone
| |
| Other names
Luteolol
Digitoflavone Flacitran Luteoline | |
| Identifiers | |
3D model (JSmol)
| |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.007.038 |
PubChem CID
| |
| UNII | |
| Properties | |
| C15H10O6 | |
| Molar mass | 286.24 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
| Infobox references | |
Natural occurrences[edit]
Luteolin is most often found in leaves, but it is also seen in rinds, barks, clover blossom, and ragweed pollen.[1] It has also been isolated from the aromatic flowering plant, Salvia tomentosa in the mint family, Lamiaceae.[2]
Dietary sources include celery, broccoli, green pepper, parsley, thyme, dandelion, perilla, chamomile tea, carrots, olive oil, peppermint, rosemary, navel oranges, and oregano.[3][4] It can also be found in the seeds of the palm Aiphanes aculeata.[5]
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