Cucurbitane-type glycosides from the fruits of Momordica charantia and their hypoglycaemic and cytotoxic activities

被引:25
作者
Zhang, Li-Jie [1 ]
Liaw, Chia-Ching [2 ]
Hsiao, Ping-Chun [1 ,3 ]
Huang, Hui-Chi [4 ]
Lin, Ming-Jen [2 ]
Lin, Zhi-Hu [1 ]
Hsu, Feng-Lin [1 ,3 ]
Kuo, Yao-Haur [1 ,5 ]
机构
[1] Natl Res Inst Chinese Med, Div Herbal Drug & Nat Prod, Taipei 112, Taiwan
[2] Starsci Biotech Co Ltd, R&D Dept, Taipei 112, Taiwan
[3] Taipei Med Univ, Grad Inst Pharmacognosy, Taipei 110, Taiwan
[4] China Med Univ, Dept Chinese Pharmaceut Sci & Chinese Med Resourc, Taichung 404, Taiwan
[5] China Med Univ, Coll Chinese Med, Grad Inst Integrated Med, Taichung 404, Taiwan
关键词
Momordica charantia; Cucurbitane; Kuguasaponins; Cytotoxicity; Hypoglycaemic activity; BITTER-MELON; TRITERPENOIDS; ADIPOSITY; LEAVES; RATS;
D O I
10.1016/j.jff.2013.11.025
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Eight new cucurbitane-type glycosides, kuguasaponins A-H (1-8), and six known compounds (9-14), were isolated by the bioassay-directed fractionation of the fruits of Momordica charantia. The structures of the compounds were established via spectroscopic analyses, including NMR, IR, and MS techniques. The stereochemistry of the isolated cucurbitanes was further determined using X-ray crystallographic analysis, NOESY experiments, and acid hydrolysis, as well as comparison with the cucurbitanes reported in the literature. The HPLC profiles of the active fraction by an ELSD detector were established and used to identify the 7 main peaks of the isolated cucurbitanes. Pharmacological studies on the anti-hyperglycaemic effects revealed that compounds 2, 3, 7, 8, and 13 exhibited strong bioactivities at 10 mu M based on the glucose uptake assay. In addition, compounds 2-5, and 14 exhibited moderate cytotoxicity against MCF-7, Doay, HEp-2, and WiDr human tumour cell lines and no activity against the M10 cell line. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:564 / 574
页数:11
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