Laboratory of Combinatorial Drug Discovery, Department of Applied Chemistry National Chiao Tung University, Hsinchu 300-10, Taiwan.
Org Biomol Chem. 2011 Apr 21;9(8):2925-37. doi: 10.1039/c0ob01126f. Epub 2011 Mar 3.
The synthesis of indoline substituted nitrobenzene on a PEG support and its further elaboration to structurally diverse benzene-fused pyrazino/diazepino indoles is disclosed. A reagent based diversification approach coupled with Pictet-Spengler type condensation reactions furnished these fused polycyclic scaffolds. Microwave irradiation was used as a means of rate acceleration for soluble polymer-supported reactions. The efficiency of these fused heterocyclic molecules to inhibit the vascular endothelial growth factor receptor 3 (VEGFR-3) was examined in vitro using kinase receptor activation enzyme-linked immunosorbant assay (KIRA-ELISA). Based on the preliminary results obtained, a small set of potential drug candidates were identified as novel leads in this therapeutic area to be further explored as anti-metastatic agents.
本文报道了在 PEG 载体上合成吲哚啉取代的硝基苯,并进一步将其拓展为结构多样的苯并吡嗪/二氮杂吲哚。通过基于试剂的多样化方法与皮克特-斯宾格勒(Pictet-Spengler)型缩合反应构建了这些稠合多环骨架。微波辐射被用作加速可溶性聚合物支撑反应的手段。通过激酶受体激活酶联免疫吸附测定(KIRA-ELISA),在体外检测了这些稠合杂环分子抑制血管内皮生长因子受体 3(VEGFR-3)的活性。根据初步结果,确定了一小部分有潜力的候选药物作为该治疗领域的新型先导化合物,以进一步探索作为抗转移剂。