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Synthesis and antitumor activity of novel N-(5-benzyl-4-(tert-butyl)thiazol-2-yl)-2-(piperazin-1-yl)acetamides

机译:新型N-(5-苄基-4-(叔丁基)噻唑-2-基)-2-(哌嗪-1-基)乙酰胺的合成和抗肿瘤活性

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摘要

A series of novel N-(5-benzyl-4-(tert-butyl) thiazol-2-yl)-2-(piperazin-1yl) acetamides were designed, synthesized and evaluated for their antitumor activities in vitro. The structures of the synthesized compounds were characterized by H-1 NMR, C-13 NMR and elemental analysis. In general, compounds 5a, 5c and 6a showed potent antiproliferative activity against HeLa (human cervical cancer) and A549 (human lung cancer) cell lines. Compound 6a, with the best inhibitory activity against HeLa cells (IC50 = 1.6 +/- 0.8 mu M), was selected to investigate the induced changes of cell morphology in the HeLa cell line by means of acridine orange (AO)/ethidium bromide (EB) double staining and cell cycle analysis using flow cytometry. The results indicated that compound 6a could induce cell apoptosis and cause G1-phase arrest in the cell division cycle.
机译:设计了一系列新的N-(5-苄基-4-(叔丁基)噻唑-2-基)-2-(哌嗪-100)乙酰胺,在体外合成和评估其抗肿瘤活性。 合成化合物的结构的特征在于H-1 NMR,C-13 NMR和元素分析。 通常,化合物5a,5c和6a显示出对Hela(人宫颈癌)和A549(人肺癌)细胞系的有效抗增殖活性。 选择具有对HeLa细胞的最佳抑制活性的化合物6a(IC50 = 1.6 +/-0.8μm),以吖啶橙(AO)/乙锭(AO)/乙锭(AO)/乙锭( EB)使用流式细胞术进行双染色和细胞循环分析。 结果表明,化合物6a可以诱导细胞凋亡并导致细胞分裂周期中的G1相停滞。

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