Two new ditetrahydrofuran lignans from Artemisia sieversiana

被引:11
作者
Zhou, Xu-Dong [1 ,2 ]
Xu, Xiang-Wei [3 ]
Shi, Lun-Yong [1 ]
Chen, Sheng-Huang [2 ]
Zeng, Ke-Wu [1 ]
Tu, Peng-Fei [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing, Peoples R China
[2] Hunan Univ Chinese Med, Sch Pharm, TCM & Ethnomed Innovat & Dev Lab, Changsha, Hunan, Peoples R China
[3] Yongkang First Peoples Hosp, Pharm Dept, Yongkang, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Asteraceae; Artemisia sieversiana; lignans; sieverlignan; anti-neuroinflammatory; STEREOCHEMISTRY; DERIVATIVES; FLAVONOIDS; TERPENOIDS;
D O I
10.1080/14786419.2020.1712384
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two new ditetrahydrofuran lignans, named sieverlignans A and B (1 and 2), together with six known ones (3-8), were isolated from the aerial parts of Artemisia sieversiana. Their structures were established on the basis of spectroscopic analysis including HRMS, NMR spectra and circular dichroism experiments. All the compounds were evaluated for their anti-neuroinflammatory effects on the lipopolysaccharides (LPS)-induced nitric oxide production in BV-2 murine microglial cells. Compound 2 exhibited the significant activity with its IC50 value of 11.9 +/- 0.8 mu M, respectively, compared to a positive control quercetin with its IC50 value of 16.0 +/- 1.1 mu M.
引用
收藏
页码:3528 / 3534
页数:7
相关论文
共 21 条
  • [1] Abulajiang Tulake Abulajiang Tulake, 2012, Journal of Chinese Pharmaceutical Sciences, V21, P360
  • [2] Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea
    Ahmed, AA
    Mahmoud, AA
    Ali, ET
    Tzakou, O
    Couladis, M
    Mabry, TJ
    Gáti, T
    Tóth, G
    [J]. PHYTOCHEMISTRY, 2002, 59 (08) : 851 - 856
  • [3] NEW UNSYMMETRICALLY SUBSTITUTED TETRAHYDROFUROFURAN LIGNANS FROM ARTEMISIA-ABSINTHIUM - ASSIGNMENT OF THE RELATIVE STEREOCHEMISTRY BY LANTHANIDE INDUCED CHEMICAL-SHIFTS
    GREGER, H
    HOFER, O
    [J]. TETRAHEDRON, 1980, 36 (24) : 3551 - 3558
  • [4] STEREOCHEMISTRY OF TETRAHYDROFUROFURAN DERIVATIVES - CIRCULAR-DICHROISM AND ABSOLUTE CONFORMATION
    HOFER, O
    SCHOLM, R
    [J]. TETRAHEDRON, 1981, 37 (06) : 1181 - 1186
  • [5] Jiangsu College of New Medicine, 1977, COMPR DICT TRAD CHIN, P627
  • [6] Bioactive lignans from Peperomia duclouxii
    Li, Na
    Wu, Jian-lin
    Hasegawa, Toshiaki
    Sakai, Jun-ichi
    Bai, Li-ming
    Wang, Li-yan
    Kakuta, Saori
    Furuya, Yumiko
    Ogura, Hirotsugu
    Kataoka, Takao
    Tomida, Akihiro
    Tsuruo, Takashi
    Ando, Masayoshi
    [J]. JOURNAL OF NATURAL PRODUCTS, 2007, 70 (04): : 544 - 548
  • [7] Two new flavonoids from Artemisia argyi with their anticoagulation activities
    Lv, Jie-Li
    Li, Zhen-Zhen
    Zhang, Lai-Bin
    [J]. NATURAL PRODUCT RESEARCH, 2018, 32 (06) : 632 - 639
  • [8] Triterpenes and lignans from Artemisia caruifolia and their cytotoxic effects on Meth-A and LLC tumor cell lines
    Ma, CM
    Nakamura, N
    Min, BS
    Hattori, M
    [J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2001, 49 (02) : 183 - 187
  • [9] Flavone glucosides from Artemisia juncea
    Okhundedaev, Bakhodir S.
    Bacher, Markus
    Mukhamatkhanova, Rimma F.
    Shamyanov, Ildar J.
    Zengin, Gokhan
    Boehmdorfer, Stefan
    Mamadalieva, Nilufar Z.
    Rosenau, Thomas
    [J]. NATURAL PRODUCT RESEARCH, 2019, 33 (15) : 2169 - 2175
  • [10] Phytochemical analysis of non-volatile fraction of Artemisia caerulescens subsp densiflora (Viv.) (Asteraceae), an endemic species of La Maddalena Archipelago (Sardinia - Italy)
    Ornano, Luigi
    Venditti, Alessandro
    Donno, Yuri
    Sanna, Cinzia
    Ballero, Mauro
    Bianco, Armandodoriano
    [J]. NATURAL PRODUCT RESEARCH, 2016, 30 (08) : 920 - 925