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首页> 外文期刊>Acta Chimica Slovenica >Synthesis and in vitro Anticancer Activity of Novel Heterocycles Utilizing Thiophene Incorporated Thioureido Substituent as Precursors
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Synthesis and in vitro Anticancer Activity of Novel Heterocycles Utilizing Thiophene Incorporated Thioureido Substituent as Precursors

机译:利用噻吩掺入硫代内酯的新杂环的合成和体外抗癌活性作为前体

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Ethyl 2-(3-allylthioureido)-4,5,6,7-tetrahydrobenzo[ b ]thiophene-3-carboxylate ( 1 ) was used as a building block for synthesis of new heterocycles. Pyrimidine and thiazole moieties were achieved upon condensation of compound 1 with various reagents such as chloroacetic acid, dietyl malonate, ninhydrin, 2,3-epoxy-2,3-dihydro-1,4-naphthoquinone, and hydrazine hydrate. The structures of the newly synthesized compounds were confirmed using spectral measurements. The prepared products were evaluated for their anticancer activity against colon HCT-116 human cancer cell line. Compounds 6 , 9 , 10a , 11 , 12 , 15 have displayed potent activity.
机译:将2-(3-烯丙基硫脲)-4,5,6,7-四氢苯并[B]噻吩-3-羧酸盐(1)用作合成新杂环的结构块。通过各种试剂如氯代乙酸,尿酸亚酮酸,茚三酮,2,3-环氧-2,3-二氢-1,4-萘醌和肼水合物在化合物1的缩合时实现嘧啶和噻唑部分。使用光谱测量确认新合成化合物的结构。评估制备的产物对抗结肠HCT-116人癌细胞系的抗癌活性。化合物6,9,10a,11,12,15显示出效率活性。

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