Structures and antiviral activities of butyrolactone derivatives isolated from Aspergillus terreus MXH-23

被引:19
作者
Ma Xinhua [1 ]
Zhu Tianjiao [1 ]
Gu Qianqun [1 ]
Xi Rui [2 ]
Wang Wei [1 ]
Li Dehai [1 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, Key Lab Marine Drugs, Chinese Minist Educ, Qingdao 266003, Peoples R China
[2] Zhangqiu Matern & Child Hlth Care Hosp, Jinan 250200, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
sponge-derived fungus; secondary metabolite; butyrolactone; anti-influenza activity; MARINE-DERIVED FUNGUS; METABOLIC PRODUCTS; A-D; SPONGE; INHIBITOR; ALKALOIDS;
D O I
10.1007/s11802-014-2324-z
中图分类号
P7 [海洋学];
学科分类号
0707 ;
摘要
A new butyrolactone derivative, namely butyrolactone VIII (1), and six known butyrolactones (2-7) were separated from the ethyl acetate (EtOAc) extract of the fermentation broth of a fungus, Aspergillus terreus MXH-23. The chemical structures of these metabolites were identified by analyzing their nuclear magnetic resonance (NMR) and mass spectrometry (MS). Known butyrolactone derivatives contain an alpha,beta-unsaturated gamma-lactone ring with alpha-hydroxyl and gamma-benzyl, and butyrolactone VIII (1) was the first butyrolactones contains alpha-benzyl and gamma-hydroxyl on alpha,beta-unsaturated lactone ring. All of the butyrolactone derivatives were tested for their anti-influenza (H1N1) effects. Derivatives 4 and 7 showed moderate antiviral activities while the newly-identified, derivative 1, did not.
引用
收藏
页码:1067 / 1070
页数:4
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