Antioxidant Hydroanthraquinones from the Marine Algal-Derived Endophytic Fungus Talaromyces islandicus EN-501

被引:54
|
作者
Li, Hong-Lei [1 ,2 ]
Li, Xiao-Ming [1 ]
Li, Xin [1 ,2 ]
Wang, Chen-Yin [3 ]
Liu, Hui [1 ,2 ]
Kassack, Matthias U. [3 ]
Meng, Ling-Hong [1 ]
Wang, Bin-Gui [1 ]
机构
[1] Chinese Acad Sci, Lab Marine Biol & Biotechnol, Qmgdao Natl Lab Marine Sci & Technol, Key Lab Expt Marine Biol,Inst Oceanol, Nanhai Rd 7, Qingdao 266071, Peoples R China
[2] Univ Chinese Acad Sci, Yuquan Rd 19A, Beijing 100049, Peoples R China
[3] Heinrich Heine Univ Dusseldorf, Inst Pharmazeut & Med Chem, Univ Str 1, D-40225 Dusseldorf, Germany
来源
JOURNAL OF NATURAL PRODUCTS | 2017年 / 80卷 / 01期
关键词
ANTHRAQUINONE DERIVATIVES; BIOACTIVE METABOLITES; SESQUITERPENES; ACID;
D O I
10.1021/acs.jnatprod.6b00797
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Five new polyhydroxylated hydroanthraquinone derivatives, namely, 8-hydroxyconiothyrinone B (1), 8,11-dihydroxyconiothyrinone B (2), 4R,8-dihydroxyconiothyrinone B (3), 4S,8-dihydroxyconiothyrinone B (4), and 4S,8-dihydroxy-10-O-methyldendryol E (5), were isolated and identified from the culture extract of Talaromyces islandicus EN-501, an endophytic fungus obtained from the inner tissue of the marine red alga Laurencia okamurai. The structures of these compounds were established on the basis of detailed interpretation of their NMR and mass spectroscopic data, and the structures and absolute configurations of compounds 1 and 2 were confirmed by X-ray crystallographic analysis, while the absolute configurations of compounds 3-5 were determined by TDDFT calculations of the ECD spectra. The antimicrobial, antioxidant, and cytotoxic activities of compounds 1-5 were evaluated.
引用
收藏
页码:162 / 168
页数:7
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