Moxifloxacin/Gatifloxacin-1,2,3-triazole-isatin Hybrids with Hydrogen-Bond Donor and Their In Vitro Anticancer Activity

被引:8
作者
Chen, Rongxing [1 ]
Zhang, Hao [2 ]
Ma, Tianwei [1 ]
Xue, Huarui [1 ]
Miao, Thong [1 ]
Chen, Liyan [1 ]
Shi, Xiangkui [1 ]
机构
[1] Xuzhou Women & Childrens Healthcare Hosp, Xuzhou 221009, Jiangsu, Peoples R China
[2] Xuzhou Cent Hosp, Dept Neurosurg, Div 2, Xuzhou 221009, Jiangsu, Peoples R China
关键词
ISATIN HYBRIDS; QUINOLONE DERIVATIVES; DESIGN;
D O I
10.1002/jhet.3670
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of novel moxifloxacin/gatifloxacin-1,2,3-triazole-isatin hybrids (8a-i) were designed, synthesized, and screened for their in vitro anticancer activity in this paper. All of the synthesized hybrids were active against A549 and HepG2 cancer cell lines, whereas the parent drugs moxifloxacin and gatifloxacin were devoid of activity. Among them, hybrid 8i (IC50: 41.1-98.3 mu M) showed considerable activity against A549, HepG2, and MCF-7 cancer cell lines, and it was no inferior to Vorinostat (IC50: 64.32 to >100 mu M) against the three cancer cell lines. Thus, this kind of hybrids has potentiality for discovery of new anticancer candidates for clinical deployment in the control and eradication of cancers.
引用
收藏
页码:2691 / 2694
页数:4
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