首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Synthesis, antitumor activity evaluation of some new N-aroyl-alpha, beta-unsaturated piperidones with fluorescence
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Synthesis, antitumor activity evaluation of some new N-aroyl-alpha, beta-unsaturated piperidones with fluorescence

机译:一些带有荧光的新型N-芳酰基-α,β-不饱和哌啶酮的合成,抗肿瘤活性评估

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摘要

Novel N-aroyl-,-unsaturated piperidones, series 1, series 2 and series 3 (featuring 2-bromo-4,5-dimethoxybenzylidene, 4-dimethylaminobenzylidene and 4-trifluoromethylbenzylidene, respectively), were synthesized as candidate cytotoxins. Most of the compounds displayed potent cytotoxicity against the human neoplastic cell lines SK-BR-3, PG-BE1, NCI-H460, MIA PaCa-2 and SW1990 in vitro, and approximately 64% of the IC50 values were lower than 5M. Among those tested, compound 1b of series 1, 3a, 3d and 3e of series 3 proved to be the most active. Importantly, 1b displayed marked inhibitory effects on tumor growth in vivo and had no apparent toxicity to mice; this was evaluated by a nude mouse PG-BE1 xenograft model. In addition, the fluorescent properties of compounds series 1-3 were investigated. The interesting fluorescence exhibited by these compounds could be useful for their visualization in tumor cells, permitting further studies on these ,-unsaturated piperidones as candidates for novel fluorescent antitumor agents.
机译:合成了新型N-芳酰基-不饱和哌啶酮系列1,系列2和系列3(分别具有2-溴-4,5-二甲氧基亚苄基,4-二甲基氨基亚苄基和4-三氟甲基亚苄基)作为候选细胞毒素。大多数化合物在体外对人瘤细胞SK-BR-3,PG-BE1,NCI-H460,MIA PaCa-2和SW1990均显示出强力的细胞毒性,IC50值的约64%低于5M。在测试的化合物中,系列1、3a,3d和3e的化合物1b被证明是活性最高的。重要的是,1b在体内对肿瘤的生长表现出明显的抑制作用,对小鼠没有明显的毒性。这是通过裸鼠PG-BE1异种移植模型评估的。另外,研究了1-3系列化合物的荧光性质。这些化合物表现出的有趣的荧光可能有助于其在肿瘤细胞中的可视化,从而允许进一步研究这些不饱和哌啶酮作为新型荧光抗肿瘤药物的候选药物。

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