Triterpenoids and Flavonoids from the Leaves of Astragalus membranaceus and Their Inhibitory Effects on Nitric Oxide Production

被引:29
作者
Wang, Zhi-Bin [1 ,4 ]
Zhai, Ya-Dong [1 ]
Ma, Zhen-Ping [1 ]
Yang, Chun-Juan [2 ,4 ]
Pan, Rong [3 ]
Yu, Jia-Li [1 ]
Wang, Qiu-Hong [1 ]
Yang, Bing-You [1 ]
Kuang, Hai-Xue [1 ]
机构
[1] Heilongjiang Univ Chinese Med, Minist Educ, Key Lab Chinese Mat Med, Harbin 150040, Peoples R China
[2] Harbin Med Univ, Coll Pharm, Harbin 150081, Peoples R China
[3] Austar Pharma LLC, Edison, NJ 08837 USA
[4] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Pharmaceut, Piscataway, NJ 08854 USA
关键词
Astragalus membranaceus; Flavonoids; Nitric oxide; Triterpenoids; LEGUMINOUS PLANTS; VAR; FRANCHETII; SAPONINS; IV; GLYCOSIDES; CONSTITUENTS; HUANGQIYENINS; ISCHEMIA; BUNGE;
D O I
10.1002/cbdv.201400371
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
Four new cycloartane triterpenes, named huangqiyegenins V and VI and huangqiyenins K and L (1-4, resp.), together with nine known triterpenoids, 5-13, and eight flavonoids, 14-21, were isolated from a 70%-EtOH extract of Astragalus membranaceus leaves. The structures of the new compounds were elucidated by detailed spectroscopic analyses, and the compounds were identified as (9,11,16,20R,24S)-11,16,25-trihydroxy-20,24-epoxy-9,19-cyclolanostane-3,6-dione (1), (9,16,24S)-16,24,25-trihydroxy-9,19-cyclolanostane-3,6-dione (2), (3,6,9,16,20R,24R)-16,25-dihydroxy-3-(-D-xylopyranosyloxy)-20,24-epoxy-9,19-cyclolanostan-6-yl acetate (3), and (3,6,9,16,24E)-26-(-D-glucopyranosyloxy)-16-hydroxy-3-(-D-xylopyranosyloxy)-9,19-cyclolanost-24-en-6-yl acetate (4). All isolated compounds were evaluated for their inhibitory activities against LPS-induced NO production in RAW264.7 macrophage cells. Compounds 1-3, 14, 15, and 18 exhibited strong inhibition on LPS-induced NO release by macrophages with IC50 values of 14.4-27.1M.
引用
收藏
页码:1575 / 1584
页数:10
相关论文
共 35 条
  • [1] Antimicrobial and Selected In Vitro Enzyme Inhibitory Effects of Leaf Extracts, Flavonols and Indole Alkaloids Isolated from Croton menyharthii
    Aderogba, Mutalib A.
    Ndhlala, Ashwell R.
    Rengasamy, Kannan R. R.
    Van Staden, Johannes
    [J]. MOLECULES, 2013, 18 (10) : 12633 - 12644
  • [2] Bi Zhi-Ming, 2007, Chinese Journal of Natural Medicines, V5, P263
  • [3] Chen HuHu Chen HuHu, 2011, Drug Evaluation Research, V34, P134
  • [4] Solvent effect in 1H NMR spectra of 3′-hydroxy-4′-methoxy isoflavonoids from Astragalus membranaceus var. mongholicus
    Du, Xingang
    Bai, Yanjing
    Liang, Hong
    Wang, Zhiying
    Zhao, Yuying
    Zhang, Qingying
    Huang, Luqi
    [J]. MAGNETIC RESONANCE IN CHEMISTRY, 2006, 44 (07) : 708 - 712
  • [5] Cycloartane-type glycosides from the roots of Astragalus caspicus Bieb.
    Fathiazad, F.
    Khosropanah, M. K.
    Movafeghi, A.
    [J]. NATURAL PRODUCT RESEARCH, 2010, 24 (11) : 1069 - 1078
  • [6] Triterpenoids
    Hill, Robert A.
    Connolly, Joseph D.
    [J]. NATURAL PRODUCT REPORTS, 2013, 30 (07) : 1028 - 1065
  • [7] Phenolic glucosides from the root of Pueraria lobata
    Hirakura, K
    Morita, M
    Nakajima, K
    Sugama, K
    Takagi, K
    Niitsu, K
    Ikeya, Y
    Maruno, M
    Okada, M
    [J]. PHYTOCHEMISTRY, 1997, 46 (05) : 921 - 928
  • [8] Hu J. F., 1995, Acta Pharmaceutica Sinica, V30, P27
  • [9] KONOSHIMA T, 1989, CHEM PHARM BULL, V37, P1550, DOI 10.1248/cpb.37.1550
  • [10] CONSTITUENTS OF LEGUMINOUS PLANTS .13. NEW TRITERPENOID SAPONINS FROM WISTARIA-BRACHYBOTRYS
    KONOSHIMA, T
    KOZUKA, M
    HARUNA, M
    ITO, K
    [J]. JOURNAL OF NATURAL PRODUCTS, 1991, 54 (03): : 830 - 836