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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of some novel benzofuran-2-yl(4,5-dihyro-3,5-substituted diphenylpyrazol-1-yl) methanones and studies on the antiproliferative effects and reversal of multidrug resistance of human MDR1-gene transfected mouse lymphoma cells in vitro.
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Synthesis of some novel benzofuran-2-yl(4,5-dihyro-3,5-substituted diphenylpyrazol-1-yl) methanones and studies on the antiproliferative effects and reversal of multidrug resistance of human MDR1-gene transfected mouse lymphoma cells in vitro.

机译:新型苯并呋喃-2-基(4,5-二氢-3,5-取代的二苯基吡唑-1-基)甲酮的合成及其对人MDR1基因转染的小鼠淋巴瘤细胞的体外抗增殖作用和多药耐药性的逆转研究。

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摘要

A new series of benzofuran-2-yl(4,5-diydro-3,5-substituted diphenylpyrazol-1-yl) methanone derivatives 8a-x by the reaction of the benzofuran-2-carbohydrazides 7 with various chalcone derivatives 3a-x using microwave irradiation has been described. The effect of synthesized compounds 8a-v was studied against human cancer cell lines for their antiproliferative activity and reversal of multidrug resistance on human MDR1-gene transfected mouse lymphoma cells. Among the 24 compounds, the 8c and 8h showed good antiproliferative activity 8b, 8f and 8k were exhibited good MDR reversal activity. The main significance of the process is easy workup process, short reaction time and high yield of the new compounds for biological interest. However, the studies on genetically modified multidrug resistant cancer cells are costly and time consuming.
机译:通过苯并呋喃-2-碳酰肼7与各种查耳酮衍生物3a-x的反应,一系列新的苯并呋喃-2-基(4,5-二吡啶-3,5-取代的二苯基吡唑-1-基)甲酮衍生物8a-x已经描述了使用微波辐射。研究了合成的化合物8a-v对人类癌细胞系的抗增殖活性以及对人类MDR1基因转染的小鼠淋巴瘤细胞多药耐药性的逆转作用。在24种化合物中,8c和8h具有良好的抗增殖活性,而8b,8f和8k具有良好的MDR逆转活性。该方法的主要意义是易于后处理,反应时间短和高产率的新化合物具有生物学意义。但是,对基因修饰的多药耐药癌细胞的研究既昂贵又费时。

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