Department of Natural Product Chemistry, Key Lab of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences , Shandong University , No. 44 West Wenhua Road , Jinan 250012 , People's Republic of China.
College of Life Sciences , Shandong Normal University , No. 88 East Wenhua Road , Jinan 250014 , People's Republic of China.
J Nat Prod. 2018 Sep 28;81(9):2041-2049. doi: 10.1021/acs.jnatprod.8b00362. Epub 2018 Aug 23.
Eleven new p-terphenyls, floricolins K-U (1-11), together with 13 biosynthetically related known compounds (12-24) were isolated from an endolichenic fungus, Floricola striata. Their structures were elucidated by extensive spectroscopic analyses and single-crystal X-ray diffraction measurements. The newly isolated p-terphenyls inhibited the growth of A2780, MCF-7, and A549 cell lines. Further evaluation for the multidrug resistance (MDR) reversal activity of compound 5 revealed it enhanced the sensitivity of MCF-7/ADR cells toward adriamycin 39-fold at 10 μM through modulating P-glycoprotein-mediated drug exclusion.
从内生真菌 Floricola striata 中分离得到 11 种新的对三联苯类化合物,floricolins K-U(1-11),以及 13 种生物合成相关的已知化合物(12-24)。通过广泛的光谱分析和单晶 X 射线衍射测量确定了它们的结构。新分离的对三联苯类化合物抑制了 A2780、MCF-7 和 A549 细胞系的生长。进一步评价化合物 5 的多药耐药 (MDR) 逆转活性表明,它通过调节 P-糖蛋白介导的药物外排,在 10 μM 时将 MCF-7/ADR 细胞对阿霉素的敏感性提高了 39 倍。