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首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >Microwave synthesis of new 3-(3-aminopropyl)-5-arylidene-2-thioxo-1,3-thiazolidine-4-ones as potential Ser/Thr protein kinase inhibitors
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Microwave synthesis of new 3-(3-aminopropyl)-5-arylidene-2-thioxo-1,3-thiazolidine-4-ones as potential Ser/Thr protein kinase inhibitors

机译:微波合成新的3-(3-氨基丙基)-5-亚芳基-2-硫代x-1,3-噻唑烷-4-酮类化合物作为潜在的Ser / Thr蛋白激酶抑制剂

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摘要

The synthesis of a series of new 3-(3-aminopropyl)-5-arylidene-2-thioxo-1,3-thiazolidine-4-ones hydrochlorides was reported. The key step of this synthetic approach involved a "one-pot two-step" protocol under microwave dielectric heating with good stereocontrol of the Knoevenagel condensation for all these new 5-arylidene rhodanines. The 18 new compounds were evaluated for their in vitro cell proliferation inhibition and also for their kinase inhibitory potencies against seven protein kinases. Two compounds (7f and 7r) were identified as potential protein kinase inhibitors.
机译:据报道合成了一系列新的3-(3-氨基丙基)-5-亚芳基-2-硫代-1,3-噻唑烷-4-酮盐酸盐。这种合成方法的关键步骤涉及在微波介电加热下进行的“一锅两步”方案,并对所有这些新的5-芳基罗丹丹酮的Knoevenagel缩合进行良好的立体控制。对18种新化合物的体外细胞增殖抑制作用以及对7种蛋白激酶的激酶抑制效力进行了评估。确定了两种化合物(7f和7r)是潜在的蛋白激酶抑制剂。

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