Three new flavonol glycosides from Fissistigma pallens

被引:5
|
作者
Nguyen Xuan Nhiem [1 ]
Ngo Sy Thinh [2 ]
Nguyen Thi Bich Thu [2 ]
Luu The Anh [3 ]
Tran Minh Ngoc, l [2 ]
Bui Huu Tai [1 ]
Pham Hai Yen [1 ]
Phan Van Kiem [1 ]
Chau Van Minh [1 ]
Park, Seonju [4 ]
Kim, Seung Hyun [4 ]
机构
[1] VAST, Inst Marine Biochem IMBC, Cau Giay, Vietnam
[2] Natl Inst Med Mat, Hoan Kiem, Vietnam
[3] Vietnam Natl Natl Univ, Cent Inst Nat Resources & Environm Studies, Hoan Kiem, Vietnam
[4] Yonsei Univ, Coll Pharm, Yonsei Inst Pharmaceut Sci, Incheon, South Korea
基金
新加坡国家研究基金会;
关键词
Fissistigma pallens; flavonol; fissflavoside A; fissflavoside B; fissflavoside C; LEAVES;
D O I
10.1080/09168451.2019.1654848
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
Three new flavonol glycosides, fissflavosides A-C (1-3), together with six known flavonol glycosides, kaempferol 3-O-alpha-L-rhamnopyranosyl-(1 -> 2)-beta-D-galactopyranoside (4), kaempferol 3-O-alpha-L-rhamnopyranosyl-(1 -> 6)-beta-D-galactopyranoside (5), kaempferol 3-O-alpha-L-rhamnopyranosyl-(1 -> 6)-beta-D-glucopyranoside (6), rhamnetin 3-O-alpha-L-rhamnopyranosyl-(1 -> 2)-beta-D-glucopyranoside (7), rutin (8), and isorhamnetin 3-O-alpha-L-rhamnopyranosyl-(1 -> 2)-beta-D-galactopyranoside (9) were isolated from the methanol extract of the Fissistigma pallens leaves. Their chemical structures were determined by 1D-, 2D-NMR, and MS data as well as in comparison with reported data in the literature. Compounds 1-9 showed weak cytotoxic activity on three human cancer cell lines, HT-29, A-2058, A-549 with IC50 ranging from 134.6 to 162.6 mu M. In addition, the antioxidant capacities of compounds were also tested by ORAC assay. All compounds showed significant antioxidant with trolox equivalents ranging from 4.4 to 8.6 mu M at the concentration of 1.0 mu M. The results indicated 7 and 8 having meaningful reducing capacity of copper (I) ions of 2.7 to 6.9 mu M at the concentrations of 1 and 2 mu M.
引用
收藏
页码:2177 / 2182
页数:6
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