Antioxidant and Anti-inflammatory Phenylpropanoid Derivatives from Calamus quiquesetinervius

被引:48
|
作者
Chang, Chao-Lin [1 ,2 ]
Zhang, Li-Jie [1 ]
Chen, Ru Yin [3 ]
Kuo, Li-Ming Yang [1 ,4 ]
Huang, Jhih-Ping [3 ]
Huang, Hui-Chi [5 ,6 ]
Lee, Kuo-Hsiung [7 ]
Wu, Yang-Chang [2 ,8 ]
Kuo, Yao-Haur [1 ,5 ,6 ]
机构
[1] Natl Res Inst Chinese Med, Div Herbal Drugs & Nat Prod, Taipei 112, Taiwan
[2] Kaohsiung Med Univ, Grad Inst Nat Prod, Kaohsiung 807, Taiwan
[3] Food Ind Res & Dev Inst, Hsinchu 300, Taiwan
[4] Taipei Med Univ, Coll Pharm, Taipei 110, Taiwan
[5] China Med Univ, Dept Chinese Med Resources, Taichung 404, Taiwan
[6] China Med Univ, Grad Inst Integrated Med, Taichung 404, Taiwan
[7] Univ N Carolina, Nat Prod Res Labs, Eshelman Sch Pharm, Chapel Hill, NC 27599 USA
[8] China Med Univ, Coll Chinese Med, Taichung 404, Taiwan
来源
JOURNAL OF NATURAL PRODUCTS | 2010年 / 73卷 / 09期
关键词
PHENOLIC CONSTITUENTS; ULTRAWEAK CHEMILUMINESCENCE; SCAVENGING ABILITY; FOOD CONSTITUENTS; AQUEOUS EXTRACTS; GLYCOSIDES; NEOLIGNANS; ALCOHOL; LEAVES; BARK;
D O I
10.1021/np100181c
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Eight new phenylpropanoid derivatives [quiquesetinerviusides A (1), B (2), C (3), D (4), and E (5), as well as quiquesetinerviusins A (6), B (7), and C (8)] and seven known compounds (8-15), were isolated from an EtOAc extract of Calamus quiquesetinervius stems. The structures of 1-8 were elucidated on the basis of 1D- and 2D-NMR spectroscopic data analysis. Bioassay results showed that 1-5 possess weak DPPH (2,2-diphenyl-1-picrylhydrazyl) scavenging activity, but potent (center dot)OH radical scavenging activity (IC(50) 3.6-8.4 mu M). Of the tested isolates, compounds 4-6 and 9 showed potent inhibition (IC(50) 9.2-29.5 mu M) of LPS-stimulated NO production when compared with a positive control substance, quercetin (IC(50) 34.5 mu M).
引用
收藏
页码:1482 / 1488
页数:7
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