Wei Fang, Zhao Bao-Xiang, Huang Bin, Zhang Lu, Sun Chun-Hui, Dong Wen-Liang, Shin Dong-Soo, Miao Jun-Ying
Institute of Organic Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.
Bioorg Med Chem Lett. 2006 Dec 15;16(24):6342-7. doi: 10.1016/j.bmcl.2006.09.008. Epub 2006 Sep 26.
We synthesized a series of novel small molecules, ethyl 1-(2'-hydroxy-3'-aroxypropyl)-3-aryl-1H-pyrazole-5-carboxylate derivatives 3a-3o, by the reaction of ethyl 3-aryl-1H-pyrazole-5-carboxylate with 2-aryloxymethylepoxide in the presence of potassium carbonate at refluxing in acetonitrile in moderate or excellent yields. We investigated the effects of all the compounds on A549 cell growth. The results showed that 15 compounds could suppress A549 lung cancer cell growth. Among them, compound 3i was the most effective small molecule in inhibiting A549 cell growth. Compound 3f might most effectively induce A549 cell differentiation. Compound 3g remarkably induced cellular vacuolation.
我们通过3-芳基-1H-吡唑-5-羧酸乙酯与2-芳氧基甲基环氧乙烷在碳酸钾存在下于乙腈中回流反应,以中等或优异的产率合成了一系列新型小分子,即1-(2'-羟基-3'-芳氧基丙基)-3-芳基-1H-吡唑-5-羧酸乙酯衍生物3a - 3o。我们研究了所有化合物对A549细胞生长的影响。结果表明,15种化合物可抑制A549肺癌细胞生长。其中,化合物3i是抑制A549细胞生长最有效的小分子。化合物3f可能最有效地诱导A549细胞分化。化合物3g显著诱导细胞空泡化。