Potent α-glucosidase inhibitors from the roots of Panax japonicus C. A. Meyer var. major

被引:49
作者
Chan, Hsiu-Hui [1 ]
Sun, Han-Dong [2 ]
Reddy, Mopur Vijaya Bhaskar [1 ]
Wu, Tian-Shung [1 ,3 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem, Tainan 70101, Taiwan
[2] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources W China, Kunming 650204, Peoples R China
[3] China Med Univ, Dept Pharm, Taichung 40402, Taiwan
关键词
Araliaceae; Panax japonicus C. A. Meyer var. major; Zu-Tziseng; Polyacetylene; Acarbose; alpha-Glucosidase inhibitors; ACTIVATES ESTROGEN-RECEPTOR; CHEMICAL-CONSTITUENTS; ABSOLUTE STRUCTURE; ACID-DERIVATIVES; GINSENG; POLYACETYLENES; FALCARINOL;
D O I
10.1016/j.phytochem.2010.04.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Bioassay-guided fractionation of the CHCl3 soluble portion of the roots of Panax japonicus C. A. Meyer var. major afforded an active fraction with inhibitory activity against baker's yeast alpha-glucosidase with an IC50 value 1.02 mg/mL. Furthermore, the active fraction isolated contained three previously unreported polyacetylenes, designated panaxjapynes A-C, together with 11 other compounds, including four polyacetylenes, five phenolic compounds, a sesquiterpenoid, and a sterol glucoside. The structures of the compounds were elucidated by spectroscopic and chemical methods. Compared with the control acarbose (IC50 677.97 mu M), six compounds were shown to be more potent alpha-glucosidase inhibitors with IC50 values in the range 22.21-217.68 mu M. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1360 / 1364
页数:5
相关论文
共 28 条
[1]
BASNET P, 1993, CHEM PHARM BULL, V41, P1238, DOI 10.1248/cpb.41.1238
[2]
Cytotoxic falcarinol oxylipins from Dendropanax arboreus [J].
Bernart, MW ;
Cardellina, JH ;
Balaschak, MS ;
Alexander, MR ;
Shoemaker, RH ;
Boyd, MR .
JOURNAL OF NATURAL PRODUCTS, 1996, 59 (08) :748-753
[3]
Cheritamine, a new N-fatty acyl tryptamine and other constituents from the stems of Annona cherimola [J].
Chen, CY ;
Chang, FR ;
Teng, CM ;
Wu, YC .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 1999, 46 (01) :77-86
[4]
Ginsenoside-Rb1 from Panax ginseng CA!Meyer activates estrogen receptor-α and -β, independent of ligand binding [J].
Cho, JY ;
Park, W ;
Lee, S ;
Ahn, W ;
Lee, Y .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (07) :3510-3515
[5]
Ginsenoside, Re of Panax ginseng possesses significant antioxidant and antihyperlipidemic efficacies in streptozotocin-induced diabetic rats [J].
Cho, William C. S. ;
Chung, Wai-Shing ;
Lee, Sally K. W. ;
Leung, Albert W. N. ;
Cheng, Christopher H. K. ;
Yue, Kevin K. M. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 550 (1-3) :173-179
[6]
GODA Y, 1987, CHEM PHARM BULL, V35, P2675
[7]
HIRAKURA K, 1992, PHYTOCHEMISTRY, V31, P899, DOI 10.1016/0031-9422(92)80036-E
[8]
POLYACETYLENES FROM THE ROOTS OF PANAX-GINSENG [J].
HIRAKURA, K ;
MORITA, M ;
NAKAJIMA, K ;
IKEYA, Y ;
MITSUHASHI, H .
PHYTOCHEMISTRY, 1991, 30 (10) :3327-3333
[9]
Hu JF, 1996, PHYTOCHEMISTRY, V43, P815, DOI 10.1016/0031-9422(96)00325-1
[10]
Anti-AIDS agents. 48. Anti-HIV activity of moronic acid derivatives and the new melliferone-related triterpenoid isolated from Brazilian propolis [J].
Ito, J ;
Chang, FR ;
Wang, HK ;
Park, YK ;
Ikegaki, M ;
Kilgore, N ;
Lee, KH .
JOURNAL OF NATURAL PRODUCTS, 2001, 64 (10) :1278-1281