Zhang Kai, Wang Peng, Xuan Li-Na, Fu Xiao-Yun, Jing Fen, Li Sha, Liu Yu-Ming, Chen Bao-Quan
Department of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, PR China.
Department of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, PR China.
Bioorg Med Chem Lett. 2014 Nov 15;24(22):5154-6. doi: 10.1016/j.bmcl.2014.09.086. Epub 2014 Oct 5.
A series of novel hybrid molecules containing 1,3,4-oxadiazole and 1,3,4-thiadiazole bearing Schiff base moiety were designed, synthesized and evaluated for their in vitro antitumor activities against SMMC-7721, MCF-7 and A549 human tumor cell lines by CCK-8 assay. The bioassay results demonstrated that most of the tested compounds showed potent antitumor activities, and some compounds exhibited stronger effects than positive control 5-fluorouracil (5-FU) against various cell lines. Among these compounds, compound 8d showed the best inhibitory effect against SMMC-7721 cells, with IC50 value of 2.84 μM. Compounds 8k and 8 n displayed highly effective antitumor activities against MCF-7 cells, with IC50 values of 4.56 and 4.25 μM, respectively. Compounds 8a and 8 n exhibited significant antiproliferative activity against A549 cells, with IC50 values of 4.11 and 4.13 μM, respectively. The pharmacological results suggest that the substituents of phenyl ring on the 1,3,4-oxadiazole are vital for modulating antiproliferative activities against various tumor cell lines.
设计、合成了一系列含有1,3,4-恶二唑和1,3,4-噻二唑并带有席夫碱部分的新型杂化分子,并通过CCK-8法评估了它们对SMMC-7721、MCF-7和A549人肿瘤细胞系的体外抗肿瘤活性。生物测定结果表明,大多数测试化合物显示出较强的抗肿瘤活性,并且一些化合物对各种细胞系表现出比阳性对照5-氟尿嘧啶(5-FU)更强的作用。在这些化合物中,化合物8d对SMMC-7721细胞显示出最佳抑制效果,IC50值为2.84 μM。化合物8k和8n对MCF-7细胞表现出高效抗肿瘤活性,IC50值分别为4.56和4.25 μM。化合物8a和8n对A549细胞表现出显著的抗增殖活性,IC50值分别为4.11和4.13 μM。药理结果表明,1,3,4-恶二唑上苯环的取代基对于调节对各种肿瘤细胞系的抗增殖活性至关重要。