首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis of novel pyrazolo(1,5-a)pyrazin-4(5H)-one derivatives and their inhibition against growth of A549 and H322 lung cancer cells.
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Synthesis of novel pyrazolo(1,5-a)pyrazin-4(5H)-one derivatives and their inhibition against growth of A549 and H322 lung cancer cells.

机译:新型吡唑并(1,5-a)吡嗪-4(5H)-one衍生物的合成及其对A549和H322肺癌细胞生长的抑制作用。

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摘要

A series of substituted pyrazolo[1,5-a]pyrazin-4(5H)-one was synthesized by the reaction of ethyl 1-(2-oxo-2-phenylethyl)-3-phenyl-1H-pyrazole-5-carboxylate derivatives and 2-(2-aminoethoxy)ethanol or 2-morpholinoethanamine in the condition of microwave-assisted one-step and solvent-free in a good yield. The structures of the compounds were determined by IR, (1)H NMR and mass spectroscopy. In addition, a representative single-crystal structure was characterized by using X-ray diffraction analysis. Preliminary biological evaluation showed that the compounds could inhibit the growth of A549 and H322 cells in dosage-dependent manners.
机译:通过1-(2-氧代-2-苯基乙基)-3-苯基-1H-吡唑-5-羧酸乙酯的反应合成了一系列取代的吡唑并[1,5-a]吡嗪-4(5H)-微波辅助一步法,无溶剂的条件下,其衍生物和2-(2-氨基乙氧基)乙醇或2-吗啉代乙胺具有良好的收率。化合物的结构通过IR,(1)H NMR和质谱确定。另外,通过使用X射线衍射分析来表征代表性的单晶结构。初步生物学评估表明,该化合物可以剂量依赖的方式抑制A549和H322细胞的生长。

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