New lasiodiplodins from mangrove endophytic fungus Lasiodiplodia sp 318#

被引:22
作者
Huang, Jiguo [1 ,2 ]
Xu, Jiayi [1 ]
Wang, Zhen [4 ]
Khan, Dilfaraz [1 ]
Niaz, Shah Iram [1 ]
Zhu, Yonghong [4 ]
Lin, Yongcheng [3 ]
Li, Jing [1 ,2 ]
Liu, Lan [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Marine Sci, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, South China Sea Resource Exploitat & Protect Coll, Guangzhou, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Histol & Embryol, Guangzhou, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
Mangrove endophytic fungus; Lasiodiplodia; lasiodiplodins; TUMOR-PROMOTING ACTIVITY; EXCOECARIA-AGALLOCHA; DERIVATIVES; THEOBROMAE; LACTONES;
D O I
10.1080/14786419.2016.1239096
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two new lasiodiplodins (1-2) together with three known analogues, were isolated from a mangrove endophytic fungus, Lasiodiplodia sp. 318(#). Their structures were established by spectroscopic techniques (1D- and 2D-NMR, HR-ESI-MS, etc.), and electronic circular dichroism. Cytotoxic activities of compounds 1-5 were evaluated in vitro. Compound 4 was the most potent, with IC50 values of 5.29M against MMQ, 13.05M against GH3. Preliminary structural-activity analysis indicated that the functional group (resorcinol-3-OH) contributed greatly to the binding of Lasiodiplodins to the cytotoxic activities. [GRAPHICS] .
引用
收藏
页码:326 / 332
页数:7
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