Chemistry Research Laboratories, Dainippon Sumitomo Pharma Co., Ltd, Konohana-ku, Osaka, Japan.
Bioorg Med Chem Lett. 2011 Mar 1;21(5):1456-8. doi: 10.1016/j.bmcl.2011.01.012. Epub 2011 Jan 8.
A series of novel 2-substituted-5-hydroxyindoles were synthesized and evaluated for their inhibitory activity against CaMKII. Structure and activity relationship results indicated that potent inhibitory activity could be achieved by modification at the para-position of the phenyl ring of the high throughput screening hit compound 2. Among the prepared compounds, we identified 14 as a novel CaMKII inhibitor with an activity stronger than that of KN-93, a known CaMKII inhibitor.
我们合成了一系列新型 2-取代-5-羟基吲哚,并对它们抑制 CaMKII 的活性进行了评估。结构与活性关系研究结果表明,对高通量筛选命中化合物 2 的苯环对位进行修饰可以获得较强的抑制活性。在所制备的化合物中,我们发现 14 是一种新型的 CaMKII 抑制剂,其活性强于已知的 CaMKII 抑制剂 KN-93。