Li Shi-Yu, Yao Lan, Lv Jian-Hua, Li Zhuang, Xu Shuai, Li Yu, Li Dan, Li Chang-Tian
Engineering Research Center of Chinese Ministry of Education for Edible and Medicinal Fungi, Jilin Agricultural University, Changchun 130118, China.
Institute of Biology, Hebei Academy of Science, Shijiazhuang 050000, China.
J Fungi (Basel). 2025 Apr 1;11(4):275. doi: 10.3390/jof11040275.
Endophytic fungi provide valuable sources for the discovery of secondary metabolites that can be used as lead compounds in drug discovery. In this study, four new sesquiterpenoids with a farnesane backbone, schizophyllol A-B (-) and schizophylloside A-B (-), together with five known analogues (-), were isolated from the plant-derived fungus sp. HM230. Their structures were established through extensive spectroscopic analyses including HR-ESI-MS and 1D and 2D NMR. The antioxidant activities of all the isolated compounds (compounds -) were evaluated via hydroxyl radical scavenging, DPPH free radical scavenging, and superoxide anion radical scavenging assays. Compounds and displayed stronger antioxidant capacities than the positive control tert-butylhydroquinone. Furthermore, the antifungal activities of the isolated compounds were evaluated against four phytopathogenic fungi: , , , and . All the test compounds demonstrated inhibitory effects; notably, compound exhibited the strongest activities against the four selected phytopathogenic fungi, with inhibitory rates ranging from 42.3% to 65.4% at 0.2 mg/mL.
内生真菌为发现可作为药物研发先导化合物的次生代谢产物提供了宝贵来源。在本研究中,从植物源真菌sp. HM230中分离出四种具有法呢烷骨架的新倍半萜类化合物,裂褶菌醇A - B(-)和裂褶菌素A - B(-),以及五种已知类似物(-)。通过包括高分辨电喷雾电离质谱(HR - ESI - MS)和一维及二维核磁共振(1D和2D NMR)在内的广泛光谱分析确定了它们的结构。通过羟基自由基清除、二苯基苦味酰基自由基(DPPH)清除和超氧阴离子自由基清除试验评估了所有分离化合物(化合物 - )的抗氧化活性。化合物 和 表现出比阳性对照叔丁基对苯二酚更强的抗氧化能力。此外,评估了分离化合物对四种植物病原真菌: 、 、 和 的抗真菌活性。所有测试化合物均表现出抑制作用;值得注意的是,化合物 对四种选定的植物病原真菌表现出最强的活性,在0.2 mg/mL时抑制率范围为42.3%至65.4%。