Glycosidase inhibitory phenolic compounds from the seed of Psoralea corylifolia

被引:72
|
作者
Oh, Kyeong Yeol [1 ]
Lee, Jin Hwan [2 ]
Curtis-Long, Marcus J.
Cho, Jung Keun [1 ]
Kim, Jun Young [1 ]
Lee, Woo Song [3 ]
Park, Ki Hun [1 ]
机构
[1] GyeongSang Natl Univ, Grad Sch, Inst Agr & Life Sci, EB NCRC,Div Appl Life Sci,Program BK21, Jinju 660701, South Korea
[2] Minist Environm, NAKDONG River Basin Environm Off, Dept Monitoring & Anal, Chang Won 641722, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Bioind Res Ctr, Jeoungeup 580185, South Korea
基金
新加坡国家研究基金会;
关键词
Glycosidase; alpha-Glucosidase inhibitor; alpha-Mannosidase inhibitor; Psoralea corylifolia; GLYCOSYLATION;
D O I
10.1016/j.foodchem.2010.01.022
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The seeds of Psoralea corylifolia were extracted into five different polar solvents: chloroform, 50% ethanol in water, ethanol, methanol and water. All extracts were evaluated for glycosidase inhibitory activity. The chloroform extract (CE) showed the lowest IC50 values against alpha-glucosidase (82.9 mu g/ml) and alpha-mannosidase (132 mu g/ml). Chromatography of CE yielded nine phenolic compounds which were identified as isovabachalcone (1), 4'-O-methylbavachalcone (2), isobavachromene (3), corylifolin (4), bavachinin (5), psoralidin (6). neobavaisoflavone (7), corylifol A (8), and bakuchiol (9). All isolated compounds, apart from compound 5, possessed alpha-glucosidase inhibitory activities. Among them, compounds 6-8 exhibited potent inhibition with IC(50)s of 13.7, 27.7 and 11.3 mu M, respectively. Furthermore, compounds 2 and 6 showed alpha-mannosidase inhibitory activity. Mechanistic analysis of their inhibition modes against alpha-glucosidase showed that compounds (6 and 7) were noncompetitive, whereas compound 8 was mixed. Furthermore, the most active glycosidase inhibitors (2,6-8) were proven to be present in the native seed in high quantities by an HPLC chromatogram. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:940 / 945
页数:6
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