motifs are frequently used as ATP-mimetic kinase inhibitors. Althought the thieno[2,3-c]pyridine scaffold also meets these criteria its use was limited so far by the availability of synthetic building blocks. Inspired by two X-ray structures of kinase bound thieno[2,3-c]pyridines we prepared a diverse collection of simple thieno[2,3-c]pyridine derivatives that could serve as starting points for future drug
具有氢键供体-受体铰链结合基序的双环杂芳基基序经常用作
ATP 模拟激酶
抑制剂。尽管
噻吩并[2,3- c ]
吡啶支架也符合这些标准,但到目前为止,它的使用受到合成构件的可用性的限制。受激酶结合的
噻吩并[2,3- c ]
吡啶的两种 X 射线结构的启发,我们制备了一系列简单的
噻吩并[2,3- c ]
吡啶衍生物,可作为未来药物发现计划的起点。在我们寻找 GRK2 激酶
抑制剂的过程中,我们还发现了一种带有 thieno[2,3- c]
吡啶部分。在结构驱动的优化过程之后,制备并表征了一系列有效且高效
配体的
抑制剂,这可以构成未来药物发现计划的基础。 图形概要