Anti-MRSA and cytotoxic activity of a new diamide compound isolated from Aspergillus sp. H30

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED Natural Product Research Pub Date : 2026-02-01 Epub Date: 2025-03-11 DOI:10.1080/14786419.2025.2478529
Long-Fen Li , Ying-Ying Hu , Xin-Zhu Wang , Qing-Zhou Meng , Pei-Pei Zhao , Qiao-Ni Chen , Ying Xu , Xue-Kui Xia
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Abstract

A new aromatic diamide compound, aspergillusin A (1), together with three known compounds, globosterol (2), ergosterol (3), and cladosporide A (4), was isolated from the crude extract of the endophytic fungi Aspergillus sp. H30. The structures were elucidated using NMR and MS data, finally, the biosynthetic pathway of compound 1 was hypothesised. Compounds 14 were tested for their antibacterial activities on six pathogenic bacteria and compound 1 was also evaluated against human non-small cell lung cancer H1299. Among them, compound 1 exhibited weak antibacterial activity against MRSA and a strong effect against the human bronchial epithelial cell line, BEAS-2B, with an IC50 value of 12.32 ± 0.37 μM.
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从曲霉sp. H30中分离的一种新的二胺化合物的抗mrsa和细胞毒活性。
从内生真菌Aspergillus sp. H30的粗提取物中分离得到一个新的芳香二胺化合物aspergillusin A(1),以及已知的3个化合物globosterol(2)、麦角甾醇(3)和cladosporide A(4)。利用核磁共振和质谱对化合物的结构进行了分析,并对化合物1的生物合成途径进行了假设。测定了化合物1 ~ 4对6种病原菌的抑菌活性,测定了化合物1对人非小细胞肺癌H1299的抑菌活性。其中,化合物1对MRSA的抑菌活性较弱,对人支气管上皮细胞系BEAS-2B的抑菌活性较强,IC50值为12.32±0.37 μM。
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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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