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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis of Dihydropyridine Derivatives under Eco-friendly Approach and Investigation of Cytotoxic Activity
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Synthesis of Dihydropyridine Derivatives under Eco-friendly Approach and Investigation of Cytotoxic Activity

机译:生态友好型方法下二氢吡啶衍生物的合成及细胞毒性活性研究

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摘要

In an effort for development of innovative biologically active agents, a sequence of 1,4-dihydropyridine analogues was synthesized through the green synthetic method. In addition, all compounds were evaluated for their cytotoxic activities against three human cancer cell lines and mouse melanoma and figured out the most active compounds. Besides, promoter reusability, easy handling of the chemical reagent, simple reaction process, time minimization, ethanol-water solvent compatibility, and cost reduction reagent are key tools for this fruitful path. Thus, these examinations recommended that dihydropyridine and their derivatives are motivating moieties for the discovery of new anticancer drugs.
机译:在开发创新的生物活性剂的努力中,通过绿色合成方法合成了一系列1,4-二氢吡啶类似物。 此外,对三种人类癌细胞系和小鼠黑色素瘤的细胞毒性,评价所有化合物的所有化合物,并计算出最活跃的化合物。 此外,启动子可重用性,易于处理化学试剂,简单的反应过程,时间最小化,乙醇 - 水溶剂相容性和成本还原试剂是该富有成效的路径的关键工具。 因此,这些考试建议二氢吡啶及其衍生物是用于发现新抗癌药物的部分。

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