Tuesday, 20 June 2017

Acacetin kháng Jurkat

Acacetin induces apoptosis in human T cell leukemia Jurkat cells

Acacetin kháng Jurkat

From Wikipedia, the free encyclopedia
Acacetin
Chemical structure of acacetin
Ball-and-stick model of acacetin
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 InfoCard100.006.867
PubChem CID
Properties
C16H12O5
Molar mass284.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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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