Benzophenone C-glucosides and gallotannins from mango tree stem bark with broad-spectrum anti-viral activity

被引:42
作者
Abdel-Mageed, Wael M. [1 ,2 ]
Bayoumi, Soad A. H. [2 ]
Chen, Caixia [1 ]
Vavricka, Christopher J. [1 ,7 ]
Li, Li [3 ,4 ]
Malik, Ajamaluddin [5 ]
Dai, Huanqin [1 ]
Song, Fuhang [1 ]
Wang, Luoqiang [1 ,7 ]
Zhang, Jingyu [1 ]
Gao, George F. [1 ]
Lv, Yali [6 ]
Liu, Lihong [6 ]
Liu, Xueting [1 ]
Sayed, Hanaa M. [2 ]
Zhang, Lixin [1 ]
机构
[1] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
[2] Assiut Univ, Fac Pharm, Dept Pharmacognosy, Assiut 71526, Egypt
[3] Chinese Acad Med Sci, Inst Mat Med, Dept Med Chem, Beijing 100050, Peoples R China
[4] Peking Union Med Coll, Beijing 100050, Peoples R China
[5] King Saud Univ, Coll Sci, Dept Biochem, Prot Res Chair, Riyadh 11451, Saudi Arabia
[6] Beijing Capital Med Univ, Beijing Chao Yang Hosp, Beijing 100020, Peoples R China
[7] Anhui Univ, Sch Life Sci, Hefei 230601, Peoples R China
基金
中国国家自然科学基金;
关键词
Mangifera indica; Anacardiaceae; Benzophenone C-glucosides; Xanthones; Mangiferin dimmer; Gallotannins; Neuraminidase inhibitors; Coxsackie protease inhibitors; Cytotoxic effect; MANGIFERA-INDICA L; ANTIINFLUENZA VIRUS ACTIVITY; NEURAMINIDASE; EXTRACT; ANTIOXIDANT; INHIBITORS; TOXICITY; LEAVES; ASSAY; ACID;
D O I
10.1016/j.bmc.2014.02.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The high mutation rate of RNA viruses has resulted in limitation of vaccine effectiveness and increased emergence of drug-resistant viruses. New effective antivirals are therefore needed to control of the highly mutative RNA viruses. The n-butanol fraction of the stem bark of Mangifera indica exhibited inhibitory activity against influenza neuraminidase (NA) and coxsackie virus 3C protease. Bioassay guided phytochemical study of M. indica stem bark afforded two new compounds including one benzophenone C-glycoside (4) and one xanthone dimer (7), together with eleven known compounds. The structures of these isolated compounds were elucidated on the basis of spectroscopic evidences and correlated with known compounds. Anti-influenza and anti-coxsackie virus activities were evaluated by determining the inhibition of anti-influenza neuraminidase (NA) from pandemic A/RI/5+/1957 H2N2 influenza A virus and inhibition of coxsackie B3 virus 3C protease, respectively. The highest anti-influenza activity was observed for compounds 8 and 9 with IC50 values of 11.9 and 9.2 mu M, respectively. Compounds 8 and 9 were even more potent against coxsackie B3 virus 3C protease, with IC50 values of 1.1 and 2.0 mu M, respectively. Compounds 8 and 9 showed weak cytotoxic effect against human hepatocellular carcinoma and human epithelial carcinoma cell lines through MTT assay. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2236 / 2243
页数:8
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