Anti-liver fibrotic lignans from the fruits of Schisandra arisanensis and Schisandra sphenanthera

被引:25
|
作者
Chen, Yu-Chen [1 ]
Liaw, Chia-Ching [1 ]
Cheng, Yuan-Bin [1 ]
Lin, Yu-Chi [1 ]
Chen, Chung-Hsiung [1 ]
Huang, Yi-Tasu [2 ]
Liou, Shorong-Shii [3 ]
Chen, Shun-Ying [4 ]
Chien, Ching-Te [4 ]
Lee, Guo-Chi [5 ]
Shen, Ya-Ching [1 ]
机构
[1] Natl Taiwan Univ, Coll Med, Sch Pharm, Taipei 100, Taiwan
[2] Natl Res Inst Chinese Med, Taipei, Taiwan
[3] Tajen Univ, Dept Pharm, Pingtung, Taiwan
[4] Taiwan Forestry Res Inst, Div Silviculture, Taipei, Taiwan
[5] Council Agr, Dept Sci & Technol, Taipei, Taiwan
关键词
Schisandra; C-18-dibenzocyclooctadiene lignans; Anti-hepatic fibrosis; SCHIZANDRA-CHINENSIS BAILL; HEPATIC STELLATE CELLS; CONSTITUENTS; GOMISIN;
D O I
10.1016/j.bmcl.2012.11.040
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Three new polyoxygenated C-18-dibenzocyclooctadiene lignans, arisanschinins M and N (1 and 2) and schisphenin A (3), together with eight related metabolites (4-11), were isolated from the fruits of Schisandra arisanensis and Schisandra sphenanthera, respectively. The structures of 1-3 were elucidated on the basis of extensive spectroscopic and 2D NMR (HSQC, HMBC, and NOESY) analyses. The configuration of the biphenyl moiety in the octadiene ring was determined by circular dichroism (CD). Compound 1 possessed an unprecedented 3-(1-hydroxypropan-2-yl)-3-methyl-1,4-dioxo-2-one lactonide ring system attaching at C-6/C-14. Pharmacological studies revealed that compounds 3, 4, 6, 7, and 10 exhibited significant anti-hepatic fibrosis activity, while 9 and 11 showed cytotoxicity against HSC-T6 cells. The bio-genetic pathway for compound 1 was also proposed. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:880 / 885
页数:6
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