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Novel Nano-sized bis-indoline Derivatives as Antitumor Agents

机译:新型纳米大小的双吲哚胺衍生物作为抗肿瘤剂

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摘要

A facile access to novel bis-(indoline-2,3-dione) was achieved via reactions of isatin with 1,3-dibromopropane. The utility of the versatile bis-(indoline-2,3-dione) in the design of new multifunctional building blocks using condensation with hydrazine derivatives was demonstrated. Moreover, a new series of bis-thiazoles and bis-thiazol-4(5H)-ones were synthesized by the reaction of bis-thiosemicarbazone derivative with various derivatives of hydrazonoyl halides. The calculations derived from X-ray diffraction patterns indicated the nanosize of the newly designed compounds. The spectral data of the formed compounds were established their structures. Also, the cytotoxic activity of the produced derivatives was screened against line MCF-7 (breast cancer cell). It was found that four derivatives from nine investigated compounds showed activity more potent than the standard drug used by 20 times in some cases.
机译:通过用1,3-二溴丙酮酸的Isatin的反应实现对新型双(吲哚-2,3-二酮)的容易进入。 展示了多功能双(Indoline-2,3-Dione)在使用肼衍生物的结露的新型多功能建筑块设计的效用。 此外,通过双硫代狄唑酮衍生物与氢肼酰卤化物的各种衍生物的反应合成了新的双噻唑和双噻唑-4(5H) - 酮。 源自X射线衍射图案的计算表明了新设计的化合物的纳米尺寸。 建立了形成的化合物的光谱数据。 此外,筛选出生产的衍生物的细胞毒性活性对线MCF-7(乳腺癌细胞)进行筛选。 发现来自九九调查化合物的四种衍生物显示出比在某些情况下使用20次的标准药物的活性。

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