红树林内生真菌Diaporthe pseudoculi HHUF 30617的抗炎代谢物。

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED
Runxin Yang, Leshi Yu, Xiaoting Xie, Gang Chen, Lu Wen
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引用次数: 0

摘要

某些红树林内生真菌具有独特的生理机制,如抗炎特性。从红树林内生真菌Diaporthe pseudooculi HHUF 30617中分离到新的聚酮n -乙酰氧基-3-(3,5-二甲基-1,3-庚二烯基)-5-氯-7-甲基-7-乙酰氧基-6,8-(2H,7H)-异喹啉二酮(1)和17个已知化合物(2-18)。利用核磁共振(NMR)谱和高分辨率电喷雾电离质谱(HRESI-MS)对新化合物的结构进行了鉴定。采用斑马鱼迁移荧光细胞计数法评价化合物的抗炎活性。结果表明上述化合物具有治疗炎症的潜力。这些发现有助于开发基于红树林内生真菌代谢物的天然海洋产品,以对抗铜毒性等条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-inflammatory metabolites from the mangrove endophytic fungus Diaporthe pseudooculi HHUF 30617.

Certain mangrove endophytic fungi have unique physiological mechanisms, such as anti-inflammatory properties. A new polyketone, namely N-acetoxyethyl-3-(3,5-dimethyl-1,3-heptadienyl)-5-chloro-7-methyl-7-acetoxy-6,8-(2H,7H)-isoquinolinedione (1), and 17 known compounds (2-18) were isolated from the mangrove endophytic fungus Diaporthe pseudooculi HHUF 30617. The structure of the new compound was elucidated using nuclear magnetic resonance (NMR) spectroscopy and high-resolution electrospray ionisation mass spectroscopy (HRESI-MS). The anti-inflammatory activities of the compounds were evaluated using the zebrafish migratory fluorescent cell count assay. The results suggest the potential of the above compounds for treating inflammation. These findings aid the development of natural marine products based on mangrove endophytic fungal metabolites to counter conditions such as copper toxicity.

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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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