Design, Synthesis and Biological Activities of Compounds Containing 1,3,4-Oxadiazole or 1,3,4-Thiadiazole

被引:14
作者
Yan, Longjia [1 ]
Li, Yongliang [1 ]
Deng, Minggao [1 ]
Chen, Anchao [1 ]
Du, Zhiyun [1 ]
Dong, Changzhi [1 ,3 ]
Chen, Huixiong [1 ,2 ]
机构
[1] Guangdong Univ Technol, Fac Light Ind & Chem Engn, Guangzhou 510006, Peoples R China
[2] Univ Paris 05, Biomed, Paris 75006, France
[3] Univ Paris Diderot, Paris 75013, France
基金
中国国家自然科学基金;
关键词
1,3,4-oxadiazole; 1,3,4-thiadiazole; anti-cancer; Src inhibitor; CARBONIC-ANHYDRASE INHIBITORS; KINASE; POTENT; DISCOVERY; SRC; SULFONAMIDE; TARGET;
D O I
10.6023/cjoc201907052
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In order to fmd new anti-tumor drugs, a series of novel 1,3,4-oxadiazole and 1,3,4-thiadiazole derivatives were designed and synthesized. The target compounds were evaluated for antitumor activity in vitro on four human cancer cell lines including B-16 (skin melanoma cells), PC-3 (human prostate cancer cells), U87 (human primary glioblastoma cells) and A549 (human non-small cell lung cancer cells). The results displayed that some of the compounds had good activities, especially, 5-((6-(4-(2-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-yl)amino)-N-(2-methoxyphenyl)-1,3,4-thiadiazole-2-carboxamide (8b) and 54(6-(4-(2-hydroxyethyl)piperaz in-1-yl)-2-methyl)pyrimidin-4-yl)amino)-N-(4-methoxy phenyl)-1,3,4-thiadiazole-2-carboxamide (8c) showed high antitumor activities against four cancer cell lines, which was better than dasatinib. These compounds were further studied for their possible target of tumor suppression.
引用
收藏
页码:731 / 739
页数:9
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