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

IF 4.4 2区 生物学 Q1 MYCOLOGY
Mycology Pub Date : 2024-10-16 eCollection Date: 2025-01-01 DOI:10.1080/21501203.2024.2397600
Xin Ouyang, Senhua Chen, Qiling Chen, Heng Guo, Lan Liu, Hongju Liu, Chong Yan
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引用次数: 0

Abstract

Four new lactones, including hypomonacid A (1) and hypomonone A-C (4-6), as well as nine known polyketide analogues (2-3 and 7-13) were obtained from endophytic fungus Hypomontagnella sp. TX-09 derived from Santalum album. 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 1 and 2 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 1 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.

抗炎多酮类化合物来源于内生真菌Hypomontagnella sp. TX-09。
从Santalum album中的内生真菌Hypomontagnella sp. x -09中获得了4个新的内酯,包括hypomononone A(1)和hypoomonone A- c(4-6),以及9个已知的聚酮类似物(2-3和7-13)。通过分析hremam和NMR光谱数据,广泛地确定了它们的平面结构。通过x射线衍射分析和改进的Mosher法结合量子化学ECD计算确定了新化合物的立体化学性质。此外,化合物1和2在50 μmol/L浓度下,通过抑制脂多糖(LPS)诱导的RAW264.7细胞NO生成而显示抗炎活性,且无细胞毒性。其中,化合物1通过抑制iNOS、TNF-α、IL-1β和IL-6的表达,抑制lps刺激小鼠巨噬细胞RAW264.7细胞炎症的产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Mycology
Mycology Medicine-Infectious Diseases
CiteScore
9.10
自引率
0.00%
发文量
18
审稿时长
13 weeks
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