Two New Alkaloids and a New Butenolide Derivative from the Beibu Gulf Sponge-Derived Fungus Penicillium sp. SCSIO 41413

被引:12
作者
Ye, Yuxiu [1 ]
Liang, Jiaqi [2 ]
She, Jianglian [2 ]
Lin, Xiuping [2 ]
Wang, Junfeng [2 ]
Liu, Yonghong [1 ,2 ]
Yang, Dehua [3 ]
Tan, Yanhui [4 ]
Luo, Xiaowei [1 ]
Zhou, Xuefeng [1 ,2 ]
机构
[1] Guangxi Univ Chinese Med, Inst Marine Drugs, Nanning 530200, Peoples R China
[2] Chinese Acad Sci, South China Sea Inst Oceanol, CAS Key Lab Trop Marine Bioresources & Ecol, Guangdong Key Lab Marine Mat Med, Guangzhou 510301, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Mat Med, Natl Ctr Drug Screening, Shanghai 201203, Peoples R China
[4] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, State Key Lab Chem & Mol Engn Med Resources, Guilin 541001, Peoples R China
基金
中国国家自然科学基金;
关键词
sponge-derived fungus; Penicillium sp; PI3K; NF-kappa B; QUINAZOLINE ALKALOIDS;
D O I
10.3390/md21010027
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Marine sponge-derived fungi have been proven to be a prolific source of bioactive natural products. Two new alkaloids, polonimides E (1) and D (2), and a new butenolide derivative, eutypoid F (11), were isolated from the Beibu Gulf sponge-derived fungus, Penicillium sp. SCSIO 41413, together with thirteen known compounds (3-10, 12-16). Their structures were determined by detailed NMR, MS spectroscopic analyses, and electronic circular dichroism (ECD) analyses. Butenolide derivatives 11 and 12 exhibited inhibitory effect against the enzyme PI3K with IC50 values of 1.7 mu M and 9.8 mu M, respectively. The molecular docking was also performed to understand the inhibitory activity, while 11 and 12 showed obvious protein/ligand-binding effects to the PI3K protein. Moreover, 4 and 15 displayed obvious inhibitory activity against LPS-induced NF-kappa B activation in RAW264.7 cells at 10 mu M.
引用
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页数:11
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