Guanacastane Diterpenoids from the Plant Endophytic Fungus Cercospora sp.

被引:28
|
作者
Feng, Yu [1 ,5 ]
Ren, Fengxia [2 ]
Niu, Shubin [1 ,5 ]
Wang, Lin [1 ,5 ]
Li, Li [3 ,4 ]
Liu, Xingzhong [1 ]
Che, Yongsheng [2 ]
机构
[1] Chinese Acad Sci, Inst Microbiol, State Key Lab Mycol, Beijing 100190, Peoples R China
[2] Beijing Inst Pharmacol & Toxicol, State Key Lab Antitox Drugs & Toxicol, Beijing 100850, Peoples R China
[3] Chinese Acad Med Sci, Inst Mat Med, Beijing 100050, Peoples R China
[4] Peking Union Med Coll, Beijing 100050, Peoples R China
[5] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2014年 / 77卷 / 04期
基金
北京市自然科学基金;
关键词
ELECTRONIC CIRCULAR-DICHROISM; PESTALOTIOPSIS-MICROSPORA; NATURAL-PRODUCTS; TAXOL; INDUCTION;
D O I
10.1021/np4009688
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Cercosporenes A-F (1-6, respectively), six new guanacastane diterpenes, including a homodimer (5) and a heterodimer (6), were isolated from the crude extract of the fungus Cercospora sp., endophytic to the medicinal plant Fallopia japonica. The structures of 1-6 were elucidated by nuclear magnetic resonance experiments, and 4 and 5 were further confirmed by X-ray crystallography. The absolute configuration of 1 and 3 was assigned by electronic circular dichroism calculations, whereas that of 6 was deduced by the application of the circular dichroism exciton chirality method. In addition to its cytotoxicity against a panel of five human tumor cell lines, HeLa, A549, MCF-7, HCT116, and T24, heterodimer 6 also induced autophagy in HCT116 cells.
引用
收藏
页码:873 / 881
页数:9
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