聚酮
真菌
立体化学
子囊菌纲
化学
生物
核磁共振波谱
绝对构型
生药学
二维核磁共振波谱
生物活性
去肽
分子构象
生物合成
生物化学
聚酮合酶
立体异构
基因组
分子模型
真菌不全
作者
Tzu-Yi Ke,Shih-Wei Wang,Zheng-Yu Lin,Govindarajan Ganesan,Cheng-Ta Lai,Juei Yu Yen,Tian-Huei Chu,Yu Chi Lin,Yuan-Bin Cheng,Tzu-Yi Ke,Shih-Wei Wang,Zheng-Yu Lin,Govindarajan Ganesan,Cheng-Ta Lai,Juei Yu Yen,Tian-Huei Chu,Yu Chi Lin,Yuan-Bin Cheng
标识
DOI:10.1021/acs.jnatprod.5c01132
摘要
Integrating genome mining with LC-MS/MS-based molecular networking analysis has revealed that the extract of the endophytic fungus Penicillium sclerotiorum represents a promising source for the discovery of new azaphilone analogues. Two rare polyketide derivatives (1 and 2), along with 11 new sclerotiorin-type azaphilones (3-13) and eight known compounds (14-21), were isolated from the macroalga-associated fungus P. sclerotiorum. The structural elucidation of these compounds was achieved using ECD, HR-ESI-MS, and NMR spectroscopic analyses. The absolute configurations of compounds 1 and 2 were determined through X-ray single-crystal diffraction. The antilymphangiogenic potential of these isolates was assessed in vitro using human lymphatic endothelial cells (LECs). Compounds 4 and 14, both nitrogenated azaphilones, exhibited significant inhibitory activity, displaying IC50 values of 5.7 ± 0.2 and 5.8 ± 0.2 μg/mL, respectively.
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