[Two new pinophol derivatives from endophytic fungus Penicillium herquei JX4 hosted in Ceriops tagal].

Q3 Pharmacology, Toxicology and Pharmaceutics Zhongguo Zhongyao Zazhi Pub Date : 2024-07-01 DOI:10.19540/j.cnki.cjcmm.20240405.202
Xian-Lei Lao, Mei-Zhu Wu, Ting Zheng, Guang-Ying Chen, Cai-Juan Zheng, Ya-Lin Chen, Jin-Qi Zhou, Shuo Feng, Xue-Ming Zhou, Xin-Ming Song
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Abstract

An OSMAC strategy was used to study secondary metabolites and anti-inflammatory activities of the endophytic fungus Penicillium herquei JX4 hosted in Ceriops tagal. The PDB ferment of fungus P. herquei JX4 was isolated, purified, and identified by using silica gel column chromatography, gel column chromatography, octadecylsilyl(ODS) column chromatography, and semi-preparative high-performance liquid chromatography. Two new pinophol derivatives, pinophol H(1) and pinophol I(2) were isolated and identified, and they were evaluated in terms of the inhibitory activities against the nitric oxide(NO) production induced by lipopolysaccharide(LPS) in mouse macrophage RAW264.7 cells. The results showed that compound 1 had significant inhibitory activity on NO production, with an IC_(50) value of 8.12 μmol·L~(-1).

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[来自寄生于 Ceriops tagal 的内生真菌 Penicillium herquei JX4 的两种新松酚衍生物]。
采用 OSMAC 策略研究了寄生在 Ceriops tagal 中的内生真菌 Herquei Penicillium JX4 的次生代谢物和抗炎活性。利用硅胶柱层析、凝胶柱层析、十八烷基硅烷基(ODS)柱层析和半制备高效液相色谱法分离、纯化和鉴定了真菌 P. herquei JX4 的 PDB 发酵产物。分离鉴定了两种新的松脂醇衍生物--松脂醇 H(1)和松脂醇 I(2),并评估了它们对小鼠巨噬细胞 RAW264.7 中脂多糖(LPS)诱导的一氧化氮(NO)生成的抑制活性。结果表明,化合物 1 对一氧化氮的产生具有显著的抑制活性,IC_(50) 值为 8.12 μmol-L~(-1)。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
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0.00%
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581
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