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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Design, synthesis and antiproliferative activity studies of novel dithiocarbamate-chalcone derivates
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Design, synthesis and antiproliferative activity studies of novel dithiocarbamate-chalcone derivates

机译:新型二硫代氨基甲酸酯-查耳酮衍生物的设计,合成和抗增殖活性研究

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摘要

A series of novel dithiocarbamate-chalcone derivates were designed, synthesized and evaluated for antiproliferative activity against three selected cancer cell lines (EC-109, SK-N-SH and MGC-803). Majority of the synthesized compounds exhibited moderate to potent activity against all the cancer cell lines assayed. Particularly, compounds II2 and II5 exhibited the excellent growth inhibition against SK-N-SH with IC50 values of 2.03 mu M and 2.46 mu M, respectively. Further mechanism studies revealed that compound II2 could obviously inhibit the proliferation of SK-N-SH cells by inducing apoptosis and arresting the cell cycle at G0/G1 phase. (C) 2016 Elsevier Ltd. All rights reserved.
机译:设计,合成和评估了一系列新颖的二硫代氨基甲酸酯-查耳酮衍生物,针对三种选定的癌细胞系(EC-109,SK-N-SH和MGC-803)具有抗增殖活性。大多数合成的化合物对所有测定的癌细胞系均表现出中等至强效的活性。特别地,化合物II2和II5表现出对SK-N-SH的优异的生长抑制,IC 50值分别为2.03μM和2.46μM。进一步的机理研究表明,化合物II2可以通过诱导细胞凋亡并将细胞周期停在G0 / G1期,从而明显抑制SK-N-SH细胞的增殖。 (C)2016 Elsevier Ltd.保留所有权利。

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