Tzu-Yi Ke, Shih‐Wei Wang, Zhengyu Lin, Ganesan Govindarajan, Cheng-Ta Lai, Juei-Yu Yen, Tian‐Huei Chu, Yu‐Chi Lin, Yuan‐Bin Cheng
High Resolution Image Download MS PowerPoint Slide 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 IC 50 values of 5.7 ± 0.2 and 5.8 ± 0.2 μg/mL, respectively.