Acacetin induces apoptosis in human T cell leukemia Jurkat cells
Acacetin kháng Jurkat
From Wikipedia, the free encyclopedia
| Names | |
|---|---|
| Preferred IUPAC name
5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
| |
| Other names
5,7-dihydroxy-2-(4-methoxyphenyl)-4H-chromen-4-one
5,7-dihydroxy-4′-methoxyflavone 4'-methoxy-5,7-dihydroxyflavone Linarigenin Acacetine Buddleoflavonol Linarisenin 4'-Methoxyapigenin Apigenin 4'-methyl ether 5,7-Dioxy-4'-methoxyflavone | |
| Identifiers | |
3D model (JSmol)
| |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.006.867 |
PubChem CID
| |
| Properties | |
| C16H12O5 | |
| Molar mass | 284.26 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
| Infobox references | |
Acacetin is an O-methylated flavone found in Robinia pseudoacacia (black locust), Turnera diffusa (damiana),[1] Betula pendula (silver birch),[2] and in the fern Asplenium normale.[3]
The enzyme apigenin 4'-O-methyltransferase uses S-adenosyl methionine and 5,7,4'-trihydroxyflavone (apigenin) to produce S-adenosylhomocysteine and 4'-methoxy-5,7-dihydroxyflavone (acacetin).
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