Bioactive Polyketide and Diketopiperazine Derivatives from the Mangrove-Sediment-Derived Fungus Aspergillus sp. SCSIO41407

被引:12
作者
Cai, Jian [1 ,2 ,3 ]
Chen, Chunmei [1 ,2 ]
Tan, Yanhui [4 ]
Chen, Weihao [1 ]
Luo, Xiaowei [5 ]
Luo, Lianxiang [6 ,7 ]
Yang, Bin [1 ,2 ,3 ]
Liu, Yonghong [1 ,2 ,3 ]
Zhou, Xuefeng [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, South China Sea Inst Oceanol, Guangdong Key Lab Marine Mat Med, CAS Key Lab Trop Marine Bioresources & Ecol, Guangzhou 510301, Peoples R China
[2] Univ Chinese Acad Sci, Coll Earth & Planetary Sci, Beijing 100049, Peoples R China
[3] Southern Marine Sci & Engn Guangdong Lab Guangzho, Guangzhou 511458, Peoples R China
[4] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China
[5] Guangxi Univ Chinese Med, Inst Marine Drugs, Nanning 530200, Peoples R China
[6] Guangdong Med Univ, Marine Biomed Res Inst, Zhanjiang 524023, Peoples R China
[7] Marine Biomed Res Inst Guangdong Zhanjiang, Zhanjiang 524023, Peoples R China
来源
MOLECULES | 2021年 / 26卷 / 16期
基金
中国国家自然科学基金;
关键词
mangrove-sediment-derived fungus; Aspergillus; polyketides; diketopiperazines; NF-kappa B; acetylcholinesterase; ALKALOIDS; ACETYLCHOLINESTERASE;
D O I
10.3390/molecules26164851
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ten polyketide derivatives (1-10), including a new natural product named (E)-2,4-dihydroxy-3-methyl-6-(2-oxopent-3-en-1-yl) benzaldehyde (1), and five known diketopiperazines (11-15), were isolated from the mangrove-sediment-derived fungus Aspergillus sp. SCSIO41407. The structures of 1-15 were determined via NMR and MS spectroscopic analysis. In a variety of bioactivity screening, 3 showed weak cytotoxicity against the A549 cell line, and 2 exhibited weak antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA). Compounds 3, 5, and 6 showed inhibition against acetylcholinesterase (AChE) with IC50 values of 23.9, 39.9, and 18.6 mu M. Compounds 11, 12, and 14 exhibited obvious inhibitory activities of lipopolysaccharide (LPS)-induced nuclear factor-kappa B (NF-kappa B) with IC50 values of 19.2, 20.9, and 8.7 mu M, and they also suppressed RANKL-induced osteoclast differentiation in bone marrow macrophages cells (BMMCs), with the concentration of 5 mu M. In silico molecular docking with AChE and NF-kappa B p65 protein were also performed to understand the inhibitory activities, and 1, 11-14 showed obvious protein/ligand-binding effects to the NF-kappa B p65 protein.
引用
收藏
页数:10
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