Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, School of Chemistry, South China Normal University, Guangzhou 510006, China.
Int J Mol Sci. 2024 May 5;25(9):5032. doi: 10.3390/ijms25095032.
One previously undescribed alkaloid, named penifuranone A (), and three known compounds (-) were isolated from the mangrove endophytic fungus SCNU-F0006. The structure of the new alkaloid () was elucidated based on extensive spectroscopic data analysis and single-crystal X-ray diffraction analysis. Four natural isolates and one new synthetic derivative of penifuranone A, compound , were screened for their antimicrobial, antioxidant, and anti-inflammatory activities. Bioassays revealed that penifuranone A () exhibited strong anti-inflammatory activity in vitro by inhibiting nitric oxide (NO) production in lipopolysaccharide-activated RAW264.7 cells with an IC value of 42.2 μM. The docking study revealed that compound exhibited an ideal fit within the active site of the murine inducible nitric oxide synthase (iNOS), establishing characteristic hydrogen bonds.
从红树林内生真菌 SCNU-F0006 中分离得到一个以前未描述的生物碱,命名为 penifuranone A (),以及三个已知化合物 (-)。新生物碱 () 的结构是根据广泛的光谱数据分析和单晶 X 射线衍射分析确定的。对四种天然分离物和一种新的 penifuranone A 的合成衍生物化合物 进行了抗微生物、抗氧化和抗炎活性筛选。生物测定表明,penifuranone A () 通过抑制脂多糖激活的 RAW264.7 细胞中一氧化氮 (NO) 的产生,在体外具有很强的抗炎活性,IC 值为 42.2 μM。对接研究表明,化合物 与小鼠诱导型一氧化氮合酶 (iNOS) 的活性位点具有理想的契合度,建立了特征性氢键。