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Novel Alkylaminopyridazine Derivatives: Synthesis and Their Anti-proliferative Effects against MCF-7 Cells

机译:新型烷基氨基哒嗪衍生物:合成及其对MCF-7细胞的抗增殖作用。

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A series of new 3-alkylamino-6-allylthio-pyridazine derivatives was synthesized through allythiolation and amino-de-halogenation and were expected to have anti-proliferative activity. 6-Allylthio-3-chloropyridazine was prepared from the reaction of 3,6-dichloropyridazine with allylmercaptan and sodium hydroxide. The alkylamines such as methylamine and the dialkylamines such as dimethylamine were introduced into the 3- position of the pyridazine ring. These new compounds showed anti-proliferative activities against MCF-7 human breast cancer cells in CCK-8 assays. These compounds are thus promising candidates for chemotherapy of breast cancer. Two compounds, 14 and 15, showed higher potencies for inhibiting growth of breast cancer cells than did 5FU. This suggests the potential anti-proliferative activity of these compounds.
机译:通过烯丙基化和氨基脱卤合成了一系列新的3-烷基氨基-6-烯丙基硫代哒嗪衍生物,并有望具有抗增殖活性。由3,6-二氯哒嗪与烯丙基硫醇和氢氧化钠反应制得6-烯丙基硫基3-氯哒嗪。将烷基胺如甲胺和二烷基胺如二甲胺引入哒嗪环的3-位。这些新化合物在CCK-8分析中显示出对MCF-7人乳腺癌细胞的抗增殖活性。因此,这些化合物是乳腺癌化学疗法的有希望的候选物。 14和15这两种化合物显示出比5FU更高的抑制乳腺癌细胞生长的能力。这表明这些化合物潜在的抗增殖活性。

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