Polyhydroxylated pyrrolidine and piperidine alkaloids from Adenophora triphylla var. japonica (Campanulaceae)

被引:77
作者
Asano, N
Nishida, M
Miyauchi, M
Ikeda, K
Yamamoto, M
Kizu, H
Kameda, Y
Watson, AA
Nash, RJ
Fleet, GWJ
机构
[1] Hokuriku Univ, Fac Pharmaceut Sci, Kanazawa, Ishikawa 9201181, Japan
[2] AFRC, Inst Grassland & Environm Res, Aberystwyth SY23 3EB, Dyfed, Wales
[3] Univ Oxford, Dyson Perrins Lab, Oxford OX1 3QY, England
关键词
Adenophora triphylla var. japonica; Campanulaceae; 1,4-dideoxy-1,4-imino-D-arabinitol (D-AB1); 6-C-butyl-DMDP; 1-deoxynojirimycin; 1-deoxymannojirimycin; alpha-1-C-ethyl-fagomine; glycosidase inhibitors;
D O I
10.1016/S0031-9422(99)00555-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adenophora triphylla var. japonica (Campanulaceae) yielded two new alkaloids, the 6-C-butyl derivative of 2R,5R-bis(hydroxymethyl)-3R,4R-dihydroxypyrrolidine (DMDP) and alpha-1-C-ethyl-fagomine, together with the known alkaloids 1,4dideoxy-1,4-imino-D-arabinitol, 1-deoxynojirimycin, and 1-deoxymannojirimycin. 6-C-Butyl-DMDP showed inhibitory activity toward almond beta-glucosidase (IC50 = 68 mu M), whereas alpha-1-C-ethyl-fagomine inhibited bovine liver beta-galactosidase (IC50 = 29 mu M) (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:379 / 382
页数:4
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