Inflammatory Inhibitory Activity of Sesquiterpenoids from Atractylodes macrocephala Rhizomes

被引:95
作者
Hoang, Le Son [1 ]
Tran, Manh Hung [1 ]
Lee, Joo-Sang [1 ]
Quynh Mai Thi Ngo [1 ]
Woo, Mi Hee [1 ]
Min, Byung Sun [1 ]
机构
[1] Catholic Univ Daegu, Coll Pharm, Drug Res & Dev Ctr, Gyeongbuk 712702, South Korea
关键词
Atractylodes macrocephala; Compositae; sesquiterpenoid; anti-inflammatory activity; RAW264.7; cell; CIRCULAR-DICHROISM; NO PRODUCTION; FERULIC ACID; CONSTITUENTS; PRINCIPLES;
D O I
10.1248/cpb.c15-00805
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Three new sesquiterpenoids, 13-hydroxyl-atractylenolide II (1), 4-ketone-atractylenolide III (2), and eudesm-4(15)-ene-7 beta,11-diol (3), along with eleven known compounds (4-14), were isolated from the rhizomes of Atractylodes macrocephala. The structures and relative configurations of 1-3 were determined by analysis of the spectroscopic data, and the absolute configurations of 1 and 2 were assigned by circular dichroism technique. The anti-inflammatory activities of these isolates were evaluated against lipopolysaccharide-induced nitric oxide production in macrophage RAW264.7 cells; compounds 4, 7, and 8 exhibited moderate efficacy with IC50 values of 48.6+/-0.5, 46.4+/-3.2, and 32.3+/-2.9 mu M, respectively.
引用
收藏
页码:507 / 511
页数:5
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