New azaphthalide and phthalide derivatives from the marine coral-derived fungus Aspergillus sp. SCSIO41405

被引:14
作者
Peng, Qingyun [1 ,2 ]
Cai, Jian [1 ,2 ]
Long, Jieyi [1 ,2 ]
Yang, Bin [1 ,2 ,3 ]
Lin, Xiuping [1 ,2 ,3 ]
Wang, Junfeng [1 ,2 ,3 ]
Xiao, Jiao [4 ]
Liu, Yonghong [1 ,2 ,3 ]
Zhou, Xuefeng [1 ,3 ]
机构
[1] Chinese Acad Sci, South China Sea Inst Oceanol, Innovat Acad South China Sea Ecol & Environm Engn, Guangdong Key Lab Marine Mat Med,CAS Key Lab Trop, Guangzhou 510301, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Southern Marine Sci & Engn Guangdong Lab Guangzho, Guangzhou 511458, Peoples R China
[4] Shenyang Pharmaceut Univ, Wuya Coll Innovat, Shenyang 110016, Peoples R China
基金
中国国家自然科学基金;
关键词
Coral-derived fungus; Azaphthalide; Phthalide; Antibacterial; Pancreatic lipase inhibition; METABOLITES; CONFIGURATION;
D O I
10.1016/j.phytol.2021.03.019
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A new azaphthalide derivative, (S)-3-hydroxy-2,7-dimethylfuro [3,4-b]pyridin-5(7H)-one (1), and a new phthalide derivative, (S)-7-hydroxy-3-((S)-1-hydroxyethyl)isobenzofuran-1(3H)-one (2), were isolated from the coral-derived fungus Aspergillus sp. SCSIO41405, together with eight known compounds (3-10). Their structures, including absolute configurations, were determined by NMR and MS spectroscopic analyses, optical rotation, calculated electronic circular dichroism (ECD) and X-ray crystal data. The isolated compounds were examined for antibacterial and enzyme inhibition activities. Compounds 7 and 8 exhibited weak antibacterial activities, and 10 displayed moderate inhibition on pancreatic lipase with an IC50 value of 15.6 mu g/mL.
引用
收藏
页码:94 / 97
页数:4
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