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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Design, Synthesis, and Evaluation of Some Novel Heterocycles Bearing Pyrazole Moiety as Potential Anticancer Agents
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Design, Synthesis, and Evaluation of Some Novel Heterocycles Bearing Pyrazole Moiety as Potential Anticancer Agents

机译:一些新型杂环部分的设计,合成和评估吡唑部分作为潜在的抗癌剂

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摘要

> 1,3‐Diphenylpyrazole‐4‐carboxylaldehyde and o ‐hydroxyacetophenone were exploited as starting materials for the synthesis of novel substituted chalconated pyrazole derivative. The proclivity of this compound towards carbon and nitrogen nucleophiles such as malononitrile, diethyl malonate, ethyl cyanoacetate, ethyl acetoacetate, semicarbazide, thiosemicarbazide, and hydroxylamine has been investigated. The structures of all synthesized compounds were ascertained by analytical and spectral data. The antitumor activity of the target synthesized compounds was tested against a panel of two human tumor cell lines, namely, hepatocellular carcinoma (liver) HepG2 and mammary gland breast MCF‐7.
机译:

1,3-二苯基吡唑-4-羧基醛和 o -Hydroxyactophenone被利用为用于合成新型取代的Chalconated的原料 吡唑衍生物。 已经研究了该化合物的促进碳和氮亲核试剂,如亚硝基,丙二酸酯,氰基乙酸乙酯,乙基乙酸乙酯,氨基脲,硫代喹甲酸和羟胺。 通过分析和光谱数据确定所有合成化合物的结构。 将靶合成化合物的抗肿瘤活性针对两种人肿瘤细胞系,即肝细胞癌(肝脏)HepG2和乳腺腺MCF-7的面板进行测试。

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