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首页> 外文期刊>Molecules >Utilization of Cyanoacetohydrazide and Oxadiazolyl Acetonitrile in the Synthesis of Some New Cytotoxic Heterocyclic Compounds
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Utilization of Cyanoacetohydrazide and Oxadiazolyl Acetonitrile in the Synthesis of Some New Cytotoxic Heterocyclic Compounds

机译:氰基乙酰肼和恶二唑基乙腈在一些新的细胞毒性杂环化合物合成中的应用

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摘要

A (pyridazinyl)acetate derivative was reacted with thiosemicarbazide and hydrazine hydrate to yield spiropyridazinone and acetohydrazide derivatives, respectively. The acetohydrazide derivative was used as a starting material for synthesizing some new heterocyclic compounds such as oxoindolinylidene, dimethylpyrazolyl, methylpyrazolyl, oxopyrazolyl, cyanoacetylacetohydrazide and oxadiazolylacetonitrile derivatives. The behavior of the cyanoacetylacetohydrazide and oxadiazolylacetonitrile derivatives towards nitrogen and carbon nucleophiles was investigated. The assigned structures of the prepared compounds were elucidated by spectral methods (IR, 1H-NMR 13C-NMR and mass spectroscopy). Some of the newly prepared compounds were tested in vitro against a panel of four human tumor cell lines, namely hepatocellular carcinoma (liver) HePG-2, colon cancer HCT-116, human prostate cancer PC3, and mammary gland breast MCF-7. Also they were tested as antioxidants. Almost all of the tested compounds showed satisfactory activity. View Full-Text
机译:使(哒嗪基)乙酸酯衍生物与硫代氨基脲和水合肼反应,分别得到螺并哒嗪酮和乙酰肼衍生物。乙酰肼衍生物用作合成一些新的杂环化合物的起始原料,例如氧代吲哚基亚烷基,二甲基吡唑基,甲基吡唑基,氧代吡唑基,氰基乙酰基乙酰肼和恶二唑基乙腈衍生物。研究了氰基乙酰乙酰肼和恶二唑基乙腈衍生物对氮和碳亲核试剂的行为。通过光谱方法(IR,1 H-NMR,13 C-NMR和质谱)阐明了制备的化合物的指定结构。在体外针对一组四种人类肿瘤细胞系(即肝细胞癌(肝)HePG-2,结肠癌HCT-116,人类前列腺癌PC3和乳腺乳腺癌MCF-7)测试了一些新制备的化合物。他们也被测试为抗氧化剂。几乎所有测试的化合物均显示令人满意的活性。查看全文

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