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 [J].
Ahmed, AA ;
Mahmoud, AA ;
Ali, ET ;
Tzakou, O ;
Couladis, M ;
Mabry, TJ ;
Gáti, T ;
Tóth, G .
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 [J].
GREGER, H ;
HOFER, O .
TETRAHEDRON, 1980, 36 (24) :3551-3558
[4]   STEREOCHEMISTRY OF TETRAHYDROFUROFURAN DERIVATIVES - CIRCULAR-DICHROISM AND ABSOLUTE CONFORMATION [J].
HOFER, O ;
SCHOLM, R .
TETRAHEDRON, 1981, 37 (06) :1181-1186
[5]  
Jiangsu College of New Medicine, 1977, COMPR DICT TRAD CHIN, P627
[6]   Bioactive lignans from Peperomia duclouxii [J].
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 .
JOURNAL OF NATURAL PRODUCTS, 2007, 70 (04) :544-548
[7]   Two new flavonoids from Artemisia argyi with their anticoagulation activities [J].
Lv, Jie-Li ;
Li, Zhen-Zhen ;
Zhang, Lai-Bin .
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 [J].
Ma, CM ;
Nakamura, N ;
Min, BS ;
Hattori, M .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2001, 49 (02) :183-187
[9]   Flavone glucosides from Artemisia juncea [J].
Okhundedaev, Bakhodir S. ;
Bacher, Markus ;
Mukhamatkhanova, Rimma F. ;
Shamyanov, Ildar J. ;
Zengin, Gokhan ;
Boehmdorfer, Stefan ;
Mamadalieva, Nilufar Z. ;
Rosenau, Thomas .
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) [J].
Ornano, Luigi ;
Venditti, Alessandro ;
Donno, Yuri ;
Sanna, Cinzia ;
Ballero, Mauro ;
Bianco, Armandodoriano .
NATURAL PRODUCT RESEARCH, 2016, 30 (08) :920-925