Triterpene compounds isolated from Acer mandshuricum and their anti-inflammatory activity

被引:43
|
作者
Ding, Yan [1 ]
Liang, Chun [1 ]
Kim, Jun Ho [2 ]
Lee, Young-Mi [2 ]
Hyun, Jae-Hee [3 ]
Kang, Hee-Kyoung [3 ]
Kim, Jeong-Ah [1 ]
Min, Byung Sun [4 ]
Kim, Young Ho [1 ]
机构
[1] Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea
[2] Wonkwang Univ, Coll Pharm, Dept Oriental Pharm, Iksan 570749, Jeonbuk, South Korea
[3] Jeju Natl Univ, Sch Med, Dept Pharmacol, Cheju 690756, South Korea
[4] Catholic Univ Daegu, Coll Pharm, Gyeongbuk 712702, South Korea
关键词
Acer mandshuricum; Aceraceae; Aceranol acetate; Triterpene; Sterol; Cytotoxic; Anti-inflammatory; TNF-alpha;
D O I
10.1016/j.bmcl.2010.01.096
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In our preliminary screening study on the anti-inflammatory activity, a new triterpene compound, aceranol acetate (1), was isolated along with five known compounds: beta-amyrin acetate (2); glutinol acetate (3); friedelin (4); glutinol (5); (3 beta)-D-glucopyranoside-stigmast-5-en-3-yl (6), from the stems and leaves of Acer mandshuricum. The structure of the new triterpene was determined to be 5 alpha,6 alpha-epidioxy-5 beta, 6 beta-epoxy-9,13-dimethyl-25,26-dinoroleanan-3 beta-ol acetate by spectroscopic studies. Compounds 2-6 were isolated from this plant for the first. Five triterpene compounds (1-5) showed significant cytotoxic activity with GI(50) in the range of 11.1-17.9 mu M, whereas steroid compound ( 6) exhibited moderate activity against four human cancer cell lines (HL-60, SK-OV-3, A549, and HT-29). Furthermore, the anti-inflammatory effects of compounds 1-6 in the non-cytotoxic concentrations (1-100 nM) were evaluated for the inhibitory activity of TNF-alpha secretion in the lipopolysaccharide (LPS)-stimulated murine RAW264.7 macrophage cell line. Among the compounds tested, compound 2 showed the strongest anti-inflammatory activity with the inhibition rate up to 38.40% at the concentration of 100 nM, whereas other five compounds (2-6) exhibited moderate activity. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1528 / 1531
页数:4
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