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(Z)-1-Aryl-3-arylamino-2-propen-1-ones Highly Active Stimulators of Tubulin Polymerization: Synthesis Structure Activity Relationship (SAR) Tubulin Polymerization and Cell Growth Inhibition Studies

机译:(Z)-1-芳基-3-芳基氨基-2-丙烯-1-酮微管蛋白聚合的高活性刺激物的合成结构活性关系(saR)微管蛋白聚合和细胞生长抑制研究

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摘要

Tubulin, the major structural component of microtubules, is a target for the development of anticancer agents. A series of (Z)-1-Aryl-3-arylamino-2-propen-1-one >(10) were synthesized and evaluated for anti-proliferative activity in cell based assay. The most active compound (Z)-1-(2- bromo-3,4,5-trimethoxyphenyl)-3-(3-hydroxy-4-methoxyphenylamino)-prop-2-en-1-one >(10ae) was tested in 20 tumor cell lines including multidrug resistant phenotype and was found to induce apoptosis in all these cell lines with similar GI50 values. Flow cytometry studies showed that >10ae arrested the cells in G2/M phase of cell cycle. In addition to G2/M block, these compounds caused microtubule stabilization like paclitaxel and induced apoptosis via activation of the caspase family. The observations made in this investigation demonstrate that (Z)-1-Aryl-3- arylamino-2-propen-1-one >(10) represents a new class of microtubule – stabilizing agents.
机译:微管是微管的主要结构组分,是抗癌剂的开发的靶标。合成了一系列(Z)-1-芳基-3-芳基-2-丙烯-2-丙烯-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-酮],并评估细胞基测定中的抗增殖活性。最活性化合物(Z)-1-(2-溴-3,4,5-三甲氧基苯基)-3-(3-羟基-4-甲氧基苯基氨基)-2-烯-1-1-1-1-酮>(10ae )在20个肿瘤细胞系中测试了,包括多药抗性表型,并发现在具有类似的Gi50值的所有这些细胞系中诱导细胞凋亡。流式细胞术研究表明,<浓度> 10ae 在细胞周期的G2 / m相中捕获细胞。除了G2 / M嵌段之外,这些化合物还引起了紫杉醇的微管稳定,并通过激活胱天蛋白酶家族诱导细胞凋亡。本研究中所做的观察结果表明(Z)-1-芳基-3-芳基-2-丙烯-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-1-普隆>(10)代表一类新的微管稳定剂。

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