Crotonkinins A and B and related diterpenoids from Croton tonkinensis as anti-inflammatory and antitumor agents

被引:41
作者
Kuo, Ping-Chung [3 ]
Shen, Yuh-Chiang [4 ]
Yang, Mei-Lin [1 ]
Wang, Su-Hui [3 ]
Thang, Tran Dinh [5 ]
Dung, Nguyen Xuan [6 ]
Chiang, Po-Cheng [7 ]
Lee, Kuo-Hsiung [7 ]
Lee, E-Jian [8 ,9 ,10 ,11 ]
Wu, Tian-Shung [1 ,2 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem, Tainan 701, Taiwan
[2] Providence Univ, Dept Appl Chem, Taichung 433, Taiwan
[3] Natl Formosa Univ, Dept Biotechnol, Yunlin 632, Taiwan
[4] Natl Res Inst Chinese Med, Taipei 112, Taiwan
[5] Vinh Univ, Dept Chem, Vinh City, Vietnam
[6] Hanoi Natl Univ, Coll Nat Sci, Dept Chem, Hanoi 10000, Vietnam
[7] Univ N Carolina, Sch Pharm, Nat Prod Res Labs, Chapel Hill, NC 27599 USA
[8] Natl Cheng Kung Univ, Dept Surg, Neurosurg Serv, Neurophysiol Lab,Med Ctr, Tainan 70101, Taiwan
[9] Natl Cheng Kung Univ, Dept Anesthesiol, Neurosurg Serv, Neurophysiol Lab,Med Ctr, Tainan 70101, Taiwan
[10] Natl Cheng Kung Univ, Inst Biomed Engn, Med Ctr, Tainan 70101, Taiwan
[11] Natl Cheng Kung Univ, Sch Med, Tainan 70101, Taiwan
来源
JOURNAL OF NATURAL PRODUCTS | 2007年 / 70卷 / 12期
关键词
D O I
10.1021/np070383f
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Cytotoxicity-guided phytochemical investigation of a methanolic extract of Croton tonkinensis afforded two new kaurane diterpenoids (1, 2) and 10 known ent-kaurane-type diterpenoids (3-12). The structures of I and 2 were based on analysis of spectroscopic and mass spectral data. Compounds 3-12 were identified by comparison of their spectroscopic and physical data with those reported in the literature. Selected compounds from this plant were examined for cytotoxic and anti-inflammatory activities. Compounds 4 and 9 showed the highest cytotoxic activity against the tested tumor cell lines. Compounds 3, 4, 6, 8, 9, and 11 had IC50 values less than 5 mu M and were more potent than the nonspecific NOS inhibitor L-NAME in inhibiting LPS-induced NO production.
引用
收藏
页码:1906 / 1909
页数:4
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