Glycosidase inhibitory flavonoids from Sophora flavescens

被引:99
作者
Kim, JH
Ryu, YB
Kang, NS
Lee, BW
Heo, JS
Jeong, IY
Park, KH [1 ]
机构
[1] Gyeongsang Natl Univ, Div Appl Life Sci, BK21 Program, Inst Agr & Life Sci,Dept Agr Chem, Jinju 660701, South Korea
[2] Korea Atom Energy Res Inst, Div Radiat Res, Jeongeup 580185, South Korea
关键词
lavandulylated flavonoid; glycosidase inhibitor; Sophora flavescens; mixed-type inhibitor; noncompetitive inhibitor;
D O I
10.1248/bpb.29.302
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The methanol extract of Sophora flavescens showed a potent glycosidase inhibitory activity. Active components were identified as well-known flavonoid antioxidants: kushenol A (1), (-)-kurarinone (2), sophoraflavanone G (3), 2'-methoxykurarinone (4), kurarinol (5), 8-prenylkaempferol (6), isoxanthohumol (7), kuraridin (8) and maackian (9). All flavonoids were effective inhibitors of alpha-glucosidase and beta-amylase. Interestingly, lavandulylated flavanones 1-5 had strong alpha-glucosidase inhibitory activities, with IC50 values of 45 mu m, 68,mu m, 37 mu m, 155 mu m and 179 mu m, respectively. Kushenol A (1) which does not bear a 4'-hvdroxy group showed selective a-glucosidase inhibitory activity. Lavandulylated chalcone, kuraridine (8), exhibited IC50 value of 57 mu M against beta-glucosidase, which is the first report of a chalcone displaying glycosidase inhibition. Results showed that 8-lavandulyl group in B-ring was a key factor of the glycosidase inhibitory activities. The inhibition pattern was noncompetitive for alpha-glucosidase, whereas mixed inhibition was observed for beta-amylase.
引用
收藏
页码:302 / 305
页数:4
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