Rega Institute for Medical Research, Katholieke Universiteit Leuven, Leuven, Belgium.
J Med Chem. 2009 Mar 12;52(5):1486-90. doi: 10.1021/jm801240d.
For establishment of the structure-activity relationship, 19 heterobicycle-coumarin conjugated compounds with the -SCH(2)- linker were synthesized and found to possess significant antiviral activities. Prominent examples included imidazopyridine-coumarin 12c, purine-coumarin 12d, and benzoxazole-coumarin 14c, which inhibited HCV replication at an EC(50) of 6.8, 2.0, and 12 microM, respectively. The heteroatoms in bicycles and the substituent effect on coumarin played essential roles.
为了建立构效关系,合成了 19 种带有-SCH(2)-连接基团的杂环香豆素共轭化合物,发现它们具有显著的抗病毒活性。突出的例子包括咪唑并吡啶香豆素 12c、嘌呤香豆素 12d 和苯并恶唑香豆素 14c,它们分别以 6.8、2.0 和 12 μM 的 EC(50)抑制 HCV 复制。杂环中的杂原子和香豆素上取代基的效应对其发挥了重要作用。