A new lupane glycoside isolated from Dendrobium officinale withα-glucosidase inhibitory activity

被引:0
作者
Yen, Pham Hai [1 ]
Hang, Dan Thi Thuy [1 ]
Tra, Dinh Thu [1 ]
Hoang, Nguyen Huy [1 ]
Bang, Ngo Anh [1 ]
Dung, Nguyen Viet [1 ]
Huong, Phan Thi Thanh [1 ]
Yen, Duong Thi Hai [1 ]
Dung, Duong Thi [1 ]
Trang, Do Thi [1 ]
Tai, Bui Huu [1 ]
Kiem, Phan Van [1 ]
机构
[1] Vietnam Acad Sci & Technol VAST, Inst Marine Biochem, Hanoi, Vietnam
关键词
Dendrobium officinale; dendrolupanoside; lupane triterpenoid; Orchidaceae; alpha-glucosidase inhibitory activity; TRITERPENOID SAPONINS;
D O I
10.1002/vjch.70020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new lupane triterpene glycoside (1) and four known compounds (2-5) were isolated from the aerial parts of Dendrobium officinale. Their chemical structures were determined to be 3-O-alpha-L-arabinopyranosylbetulinic acid 28-O-beta-D- glucopyranosyl-(1 -> 6)-beta-D-glucopyranosyl ester (1), 3-O-alpha-L-arabinopyranosylbetulinic acid 28-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-glucopyranosyl-(1 -> 6)-beta- D-glucopyranosyl ester (2), 3-O-beta-D-glucopyranosylbetulinic acid 28-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-glucopyranosyl-(1 -> 6)-beta-D-glucopyranosyl ester (3), 6 alpha-hydroxylup-20(29)-en-3-on 28-oic acid (4), and lupeol (5) by analyzing the HR-ESI-MS, 1D and 2D NMR spectra including COSY and NOESY. Compounds 1, 2 and 4 showed weak alpha-glucosidase inhibitory activity with IC50 values ranging from 87.5 to 98.2 mu M.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Phenanthrenes from Dendrobium senile and their pancreatic lipase inhibitory activity
    Pann Phyu, Myat
    Kongkatitham, Virunh
    Mekboonsonglarp, Wanwimon
    Likhitwitayawuid, Kittisak
    Sritularak, Boonchoo
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2022, 24 (07) : 697 - 702
  • [32] A new citryl glycoside from Gastrodia elata and its inhibitory activity on GABA transaminase
    Choi, Jung-Hyun
    Lee, Dong-Ung
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2006, 54 (12) : 1720 - 1721
  • [33] Triterpenoids with α-glucosidase inhibitory activity from Artemisia argyi
    Zhang, Lai-Bin
    Chang, Jia-Jing
    Guo, Li-Min
    Lv, Jie-Li
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2020, 22 (03) : 241 - 248
  • [34] Partial characterization and immunomodulatory activity of polysaccharides from the stem of Dendrobium officinale (Tiepishihu) in vitro
    Xia, Linjing
    Liu, Xiaofei
    Guo, Huiyuan
    Zhang, Hao
    Zhu, Jun
    Ren, Fazheng
    JOURNAL OF FUNCTIONAL FOODS, 2012, 4 (01) : 294 - 301
  • [35] New triterpenoid saponins with strong α-glucosidase inhibitory activity from the roots of Gypsophila oldhamiana
    Luo, Han-Guang
    Ma, Li
    Kong, Ling-Yi
    BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (06) : 2912 - 2920
  • [36] New lignans and acetophenone derivatives with α-glucosidase inhibitory activity from the leaves of Melicope patulinervia
    Vu, Van-Tuan
    Manh-Tuyen Nguyen
    Nguyen-Minh Khoi
    Xu, Xiao-Juan
    Kong, Ling-Yi
    Luo, Jian-Guang
    FITOTERAPIA, 2021, 148
  • [37] α-Glucosidase inhibitory and α-amylase inhibitory activities of compounds isolated from Uvaria rufa Blume
    Teerapongpisan, Passakorn
    Suthiphasilp, Virayu
    Maneerat, Tharakorn
    Charoensup, Rawiwan
    Duangyod, Thidarat
    Andersen, Raymond J.
    Laphookhieo, Surat
    NATURAL PRODUCT RESEARCH, 2022, 36 (23) : 6039 - 6043
  • [38] Cytotoxic and Antifungal Constituents Isolated from the Metabolites of Endophytic Fungus DO14 from Dendrobium officinale
    Wu, Ling-Shang
    Jia, Min
    Chen, Ling
    Zhu, Bo
    Dong, Hong-Xiu
    Si, Jin-Ping
    Peng, Wei
    Han, Ting
    MOLECULES, 2016, 21 (01):
  • [39] Extraction, purification and antioxidant activity of novel polysaccharides from Dendrobium officinale by deep eutectic solvents
    Liang, Jing
    Zeng, Yingjie
    Wang, Hongfeng
    Lou, Wenyong
    NATURAL PRODUCT RESEARCH, 2019, 33 (22) : 3248 - 3253
  • [40] Determination of α-glucosidase inhibitory activity from selected Fabaceae plants
    Dej-adisai, Sukanya
    Pitakbut, Thanet
    PAKISTAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2015, 28 (05) : 1679 - 1683