Infection Control Research Center, Korea Research Institute of Bioscience and Biotechnology, Jeongeup 580-185, Republic of Korea.
Bioorg Med Chem. 2013 Jul 1;21(13):3730-7. doi: 10.1016/j.bmc.2013.04.026. Epub 2013 Apr 22.
SARS-CoV 3CL(pro) plays an important role in viral replication. In this study, we performed a biological evaluation on nine phlorotannins isolated from the edible brown algae Ecklonia cava. The nine isolated phlorotannins (1-9), except phloroglucinol (1), possessed SARS-CoV 3CL(pro) inhibitory activities in a dose-dependently and competitive manner. Of these phlorotannins (1-9), two eckol groups with a diphenyl ether linked dieckol (8) showed the most potent SARS-CoV 3CL(pro) trans/cis-cleavage inhibitory effects (IC(50)s = 2.7 and 68.1 μM, respectively). This is the first report of a (8) phlorotannin chemotype significantly blocking the cleavage of SARS-CoV 3CL(pro) in a cell-based assay with no toxicity. Furthermore, dieckol (8) exhibited a high association rate in the SPR sensorgram and formed extremely strong hydrogen bonds to the catalytic dyad (Cys145 and His41) of the SARS-CoV 3CL(pro).
SARS-CoV 3CL(pro) 在病毒复制中发挥重要作用。在这项研究中,我们对从食用褐藻昆布中分离得到的 9 种岩藻多酚进行了生物学评价。除焦性没食子酚(1)外,这 9 种分离得到的岩藻多酚(1-9)均以剂量依赖和竞争的方式表现出对 SARS-CoV 3CL(pro)的抑制活性。在这些岩藻多酚(1-9)中,两个具有二苯醚连接的二岩藻素基团的 Eckol(8)显示出最强的 SARS-CoV 3CL(pro)转/顺式切割抑制作用(IC50 分别为 2.7 和 68.1 μM)。这是首次报道一种(8)岩藻多酚化学型在细胞测定中显著阻断 SARS-CoV 3CL(pro)的切割,且无毒性。此外,二岩藻素(8)在 SPR 传感器图谱中表现出高结合率,并与 SARS-CoV 3CL(pro)的催化二联体(Cys145 和 His41)形成极强的氢键。