Araliaarmoside: A New Triterpene Glycoside Isolated From the Leaves of Aralia armata

被引:4
作者
Pham Hai Yen [1 ,2 ]
Nguyen Thi Cuc [1 ]
Phan Thi Thanh Huong [1 ]
Nguyen Xuan Nhiem [1 ,2 ]
Nguyen Thi Hong Chuong [3 ]
Giang Thi Kim Lien [4 ]
Bui Huu Tai [1 ,2 ]
Nguyen Van Tuyen [5 ]
Chau Van Minh [1 ]
Phan Van Kiem [1 ,2 ]
机构
[1] Vietnam Acad Sci & Technol VAST, Inst Marine Biochem, Hanoi, Vietnam
[2] Vietnam Acad Sci & Technol VAST, Grad Univ Sci & Technol, Hanoi, Vietnam
[3] Univ Danang, Univ Educ, Danang, Vietnam
[4] Univ Danang, Danang, Vietnam
[5] Viemam Acad Sci & Technol VAST, Inst Chem, Hanoi, Vietnam
关键词
Araliaceae; Aralia armata; araliaarmoside; glycoside A; triterpene glycoside; cytotoxic activity; ROOT BARK; SAPONINS; FLOWERS;
D O I
10.1177/1934578X20953300
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
One new oleanane-type triterpene glycoside, oleanolic acid-[28-O-beta-d-glucopyranosyl]-3-O-[beta-D-glucopyranosyl(1 -> 6)-beta-D-glucopyranosyl](1 -> 3)[a-l-arabinofuranosyl(1.4)]-beta-D-glucuronopyranoside (1), and 3 known ones {oleanolic acid-[28-O-beta-d-glucopyranosyl]-3-O-[beta-D-galactopyranosyl(1.3)]-[beta ss-D-glucopyranosyl(1.2)]-beta-D-glucuronopyranoside (2) chikusetsusaponin IVa methyl ester (3), and chikusetsusaponin IV (4)} were isolated from the leaves of Aralia armata. Their chemical structures were elucidated using a combination of high-resolution electrospray ionization mass spectrometry, 1-dimensional and 2-dimensional nuclear magnetic resonance (NMR) spectral data, as well as comparison with data in the previous literature. This is the first report of full NMR spectroscopic data of 2. Compounds 1-4 displayed weak cytotoxic activity toward KB and HepG2 cell lines, with half-maximal inhibitory concentration50 values ranging from 24.2 +/- 0.3 to 32.6 +/- 0.8 mu M in in vitro assay.
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页数:5
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