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.
引用
收藏
页数:5
相关论文
共 11 条
  • [1] New antioxidant and antiglycation active triterpenoid saponins from the root bark of Aralia taibaiensis
    Bi, Linlin
    Tian, Xiangrong
    Dou, Fang
    Hong, Liangjian
    Tang, Haifeng
    Wang, Siwang
    [J]. FITOTERAPIA, 2012, 83 (01) : 234 - 240
  • [2] Chi VV, 2012, DICT VIETNAMESE MED, P956
  • [3] Clement JA, 2014, CURR TOP MED CHEM, V14, P2783
  • [4] TRITERPENOID GLUCURONIDE SAPONINS FROM ROOT BARK OF ARALIA-ARMATA
    HU, M
    OGAWA, K
    SASHIDA, Y
    XIAO, PG
    [J]. PHYTOCHEMISTRY, 1995, 39 (01) : 179 - 184
  • [5] Herbicidal and Cytotoxic Constituents from Aralia armata (WALL.) SEEM
    Miao, Hui
    Sun, Yongyan
    Yuan, Yunfei
    Zhao, Huanhuan
    Wu, Jiao
    Zhang, Weiyun
    Zhou, Lijuan
    [J]. CHEMISTRY & BIODIVERSITY, 2016, 13 (04) : 437 - 444
  • [6] Rengifo CM, 2017, PHYTOCHEMISTRY, V140, P166, DOI DOI 10.1016/J.PHYT0CHEM.2017.04.013
  • [7] SHAO CJ, 1989, CHEM PHARM BULL, V37, P311
  • [8] Facile discrimination of aldose enantiomers by reversed-phase HPLC
    Tanaka, Takashi
    Nakashima, Tatsuya
    Ueda, Toshihisa
    Tomii, Kenji
    Kouno, Isao
    [J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2007, 55 (06) : 899 - 901
  • [9] Trang DT, 2015, J MED MAT HANOI, V1, P12
  • [10] REVISED STRUCTURES OF TRITERPENOID SAPONINS FROM THE FLOWERS OF CALENDULA-OFFICINALIS
    VIDALOLLIVIER, E
    BALANSARD, G
    FAURE, R
    BABADJAMIAN, A
    [J]. JOURNAL OF NATURAL PRODUCTS, 1989, 52 (05): : 1156 - 1159