Biologically active constituents from the fruiting body of Taiwanofungus camphoratus

被引:38
作者
Shi, Li-Shian [2 ]
Chao, Chih-Hua [1 ]
Shen, De-Yang [1 ]
Chan, Hsiu-Hui [1 ]
Chen, Chou-Hsiung [1 ]
Liao, Yu-Ren [1 ]
Wu, Shwu-Jen [3 ]
Leu, Yann-Lii [4 ]
Shen, Yuh-Chiang [5 ]
Kuo, Yao-Haur [5 ]
Lee, E-Jian [6 ,7 ]
Qian, Keduo [10 ]
Wu, Tian-Shung [1 ,8 ,9 ]
Lee, Kuo-Hsiung [8 ,9 ,10 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem, Tainan 701, Taiwan
[2] Natl Formosa Univ, Dept Biotechnol, Yunlin 632, Taiwan
[3] Chung Hua Univ Med Technol, Dept Med Technol, Tainan 717, Taiwan
[4] Chang Gung Univ, Grad Inst Nat Prod, Nat Prod Lab, Tao Yuan 333, Taiwan
[5] Natl Res Inst Chinese Med, Taipei 112, Taiwan
[6] Natl Cheng Kung Univ, Med Ctr, Dept Surg, Tainan 701, Taiwan
[7] Sch Med, Tainan 701, Taiwan
[8] China Med Univ & Hosp, Chinese Med Res & Dev Ctr, Taichung, Taiwan
[9] China Med Univ & Hosp, Dept Pharm, Taichung, Taiwan
[10] Univ N Carolina, UNC Eshelman Sch Pharm, Nat Prod Res Labs, Chapel Hill, NC 27599 USA
关键词
Taiwanofungus camphoratus; Fruiting bodies; Anti-inflammatory; NOX; ROS; Cytotoxicity; OXYGEN SPECIES PRODUCTION; ANTRODIA-CINNAMOMEA; TRITERPENOIDS; NEUTROPHILS; INHIBITION;
D O I
10.1016/j.bmc.2010.10.032
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
Five new benzenoids, benzocamphorins A-E(1-5), and 10 recently isolated triterpenoids, camphoratins A-J (16-25), together with 23 known compounds including seven benzenoids (6-12), three lignans(13-15), and 13 triterpenoids (26-38) were isolated from the fruiting body of Taiwanofungus camphoratus. Their structures were established by spectroscopic analysis. Selected compounds were examined for cytotoxic and anti-inflammatory activities. Compounds 9 and 21 showed moderate cytotoxicity against MCF-7 and Hep2 cell lines with ED50 values of 3.4 and 3.0 mu g/mL, respectively. Compounds 21, 25, 26, 29-31, 33, and 36 demonstrated potent anti-inflammatory activity by inhibiting lipopolysaccharide (LPS)-induced nitric oxide (NO) production with IC50 values of 2.5, 1.6, 3.6, 0.6, 4.1, 4.2, 2.5, and 1.5 mu M, respectively, which were better than those of the nonspecific nitric oxide synthase (NOS) inhibitor N-nitro-L-arginine methyl ester (L-NAME) (IC50: 25.8 mu M). These results may substantiate the use of T. camphoratus in traditional Chinese medicine (TCM) for the treatment of inflammation and cancer-related diseases. The newly discovered compounds deserve further development as anti-inflammatory candidates. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:677 / 683
页数:7
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