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源自内生真菌sp. TX-09的抗炎聚酮化合物。

Anti-inflammatory polyketides from derived endophytic fungus sp. TX-09.

作者信息

Ouyang Xin, Chen Senhua, Chen Qiling, Guo Heng, Liu Lan, Liu Hongju, Yan Chong

机构信息

School of Pharmacy, Guangdong Medical University, Dongguan, China.

School of Marine Sciences, Sun Yat-sen University, Zhuhai, China.

出版信息

Mycology. 2024 Oct 16;16(2):918-928. doi: 10.1080/21501203.2024.2397600. eCollection 2025.

Abstract

Four new lactones, including hypomonacid A () and hypomonone A-C (), as well as nine known polyketide analogues ( and ) were obtained from endophytic fungus sp. TX-09 derived from . Their planar structures were extensively established by analysing HRESIMS and NMR spectroscopic data. Stereochemistry of new compounds was determined by X-ray diffraction analysis and modified Mosher's method in combination with quantum-chemical ECD calculation. In addition, compounds and showed anti-inflammatory activity by inhibition of lipopolysaccharide (LPS)-induced NO production in RAW264.7 cells at 50 μmol/L without cytotoxicity. Among them, compound inhibited the production of LPS-stimulated inflammation in mouse macrophage RAW264.7 cells by suppressing the expression of iNOS, TNF-α, IL-1β, and IL-6.

摘要

从来源于[具体来源未给出]的内生真菌[真菌名称未给出]TX-09中获得了四种新的内酯,包括次单酸A([具体结构未给出])和次单酮A - C([具体结构未给出]),以及九种已知的聚酮类似物([具体结构未给出])。通过分析高分辨电喷雾电离质谱(HRESIMS)和核磁共振(NMR)光谱数据广泛确定了它们的平面结构。新化合物的立体化学通过X射线衍射分析以及改良的莫舍尔方法结合量子化学电子圆二色(ECD)计算来确定。此外,化合物[具体化合物未给出]和[具体化合物未给出]在50μmol/L时通过抑制脂多糖(LPS)诱导的RAW264.7细胞中一氧化氮(NO)的产生显示出抗炎活性且无细胞毒性。其中,化合物[具体化合物未给出]通过抑制诱导型一氧化氮合酶(iNOS)、肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的表达,抑制了LPS刺激的小鼠巨噬细胞RAW264.7细胞中的炎症产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b3/12096673/987959d2513f/TMYC_A_2397600_F0001_B.jpg

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