从蘑菇 Lanmaoa asiatica 中分离出的真菌 Pestalotiopsis clavata JSQ 12 的两种烯基苯酚衍生物。

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED
Natural Product Research Pub Date : 2025-08-01 Epub Date: 2024-06-13 DOI:10.1080/14786419.2024.2367012
Jing Tang, Rui Xu, Hao Ma, Shuai-Ming Zhu, Fu-Yao Luo, Xue Zhao, Ya-Shuai Kang, Yuan-Wei Gao, Yu Yang, Chang-Wei Li
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引用次数: 0

摘要

从 Pestalotiopsis clavata JSQ 12 真菌的培养物中分离出了两种新的烯基苯酚衍生物,即 pestalol F (1) 和 pestalol G (2),以及两种已知化合物,即 pestalachloride A (3) 和 pestalotiopsin J (4)。这些化合物的结构主要是通过 MS、NMR 和特定旋转数据分析阐明的。这些 Pestalotiopsis clavata 的次级代谢产物是首次报道。化合物 2 对 MCF-7 细胞株显示出有趣的细胞毒性活性,IC50 值为 29.16 μM;化合物 3 对 A549 细胞株显示出中等程度的活性,IC50 值为 35.71 μM。阳性对照 5-FU 对 MCF-7 和 A549 细胞株有细胞毒性作用,IC50 值分别为 26.70 和 26.07 μM。化合物 1 和 2 对金黄色葡萄球菌具有温和的抗菌活性,其 MIC 值分别为 128 和 64 μg/mL(阳性对照青霉素的 MIC 值为 0.016 μg/mL)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two alkenyl phenol derivatives from the fungus Pestalotiopsis clavata JSQ 12 isolated from the mushroom Lanmaoa asiatica.

Two new alkenyl phenol derivatives, namely pestalol F (1) and pestalol G (2), along with two known compounds, pestalachloride A (3) and pestalotiopsin J (4), were isolated from the culture of the fungus Pestalotiopsis clavata JSQ 12. The structures of these compounds were primarily elucidated by MS, NMR and specific rotation data analysises. These secondary metabolites of Pestalotiopsis clavata were reported for the first time. Compound 2 displayed interesting cytotoxic activity against MCF-7 cell line with the IC50 value of 29.16 μM, whereas compound 3 exhibited moderate activity towards A549 cell line with the IC50 value of 35.71 μM. The positive control 5-FU showed cytotoxic effects on MCF-7 and A549 cell lines with the respective IC50 values of 26.70 and 26.07 μM. Compounds 1 and 2 displayed mild antibacterial activities against Staphylococcus aureus with MIC values of 128 and 64 μg/mL (MIC of positive control, penicillin, was 0.016 μg/mL), respectively.

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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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