Kinobeon A as a potent tyrosinase inhibitor from cell culture of safflower:: In vitro comparisons of kinobeon A with other putative inhibitors

被引:0
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作者
Kanehira, T
Takekoshi, S [1 ]
Nagata, H
Osamura, RY
Homma, T
机构
[1] Tokai Univ, Sch Med, Dept Pathol, Kanagawa 2591193, Japan
[2] Tokai Univ, Grad Sch Engn, Dept Appl Chem, Kanagawa 2591100, Japan
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D O I
暂无
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Kinobeon A is produced from cell cultures of the medicinal plant, safflower. Mushroom tyrosinase activity was inhibited in a concentration-dependent manner when treated with kinobeon A using L-tyrosine or L-3, 4-dihydroxyphenylalannine (L-DOPA) as substrates. IC50 values were 22 muM (substrate: L-tyrosine) and 27 muM (L-DOPA). Inhibition of human tyrosinase activity also increased with increasing concentrations of kinobeon A using L-DOPA as the substrate, with an IC50 value of 2.5 muM. Kinobeon A was a more potent competitive inhibitor than kojic acid, arbutin or L-ascorbic acid for both mushroom and human tyrosinase as determined from Lineweaver-Burk plots. These results suggested that kinobeon A could be a potent natural tyrosinase inhibitor.
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页码:457 / 459
页数:3
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