Microascones, Decahydrofluorene-Class Alkaloids from the Marine-Derived Fungus Microascus sp. SCSIO 41821

被引:2
|
作者
Yao, Fei-Hua [1 ,2 ]
Liang, Xiao [1 ,3 ]
Shen, Wen-Bin [4 ]
Lu, Xin-Hua [4 ]
Li, Guo-Chao [4 ]
Qi, Shu-Hua [1 ,3 ]
机构
[1] Chinese Acad Sci, South China Sea Inst Oceanol, CAS Key Lab Trop Marine Bioresources & Ecol, Guangdong Key Lab Marine Mat Med, Guangzhou 510301, Guangdong, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Southern Marine Sci & Engn Guangdong Lab Guangzhou, Guangzhou 511458, Peoples R China
[4] New Drug Res & Dev Ctr North China Pharmaceut Grp, Natl Engn Res Ctr Microbial Med, Shijiazhuang Microbial Drugs Technol Innovat Ctr, Hebei Synthet Biol High Energy Level Technol Innov, Shijiazhuang 050015, Hebei, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2024年 / 87卷 / 04期
基金
中国国家自然科学基金;
关键词
ANTITUBERCULAR ALKALOIDS; HIRSUTELLONES;
D O I
10.1021/acs.jnatprod.3c00984
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Eight new decahydrofluorene-class alkaloids, microascones A and B (1 and 2), 2,3-epoxyphomapyrrolidone C (3), 14,16-epiascomylactam B (4), 24-hydroxyphomapyrrolidone A (5), and microascones C-E (6-8), along with five known analogs (9-13) were isolated from the marine-derived fungus Microascus sp. SCSIO 41821. Compounds 1 and 2 have an unprecedented complex macrocyclic alkaloid skeleton with a 6/5/6/5/6/5/13 polycyclic system. Their structures and absolute configurations were determined by spectroscopic analysis, quantum chemical calculations of ECD spectra, and C-13 NMR chemical shifts. Compounds 10-13 showed selective enzyme inhibitory activity against PTPSig, PTP1B, and CDC25B, and 4, 9, and 10 exhibited strong antibacterial activity against seven tested pathogens. Their structure-bioactivity relationship was discussed, and a plausible biosynthetic pathway for 1-8 was also proposed.
引用
收藏
页码:810 / 819
页数:10
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