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作 者:Guo Qiang Hu Xiao Kui Wu Guo Qiang Wang Nan Nan Duan Xiao Yi Wen Tie Yao Cao Yin Jun Wang Wei Song Qiang Xie Wen Long Huang
机构地区:[1]Institute of Chemistry&Biology,Henan University,Kaifeng 475001,China [2]China Pharmaceutical University,Nanjing 210009,China
出 处:《Chinese Chemical Letters》2012年第5期515-517,共3页中国化学快报(英文版)
基 金:supported by the National Natural Science Foundation of China(Nos20872028 and 21072045)
摘 要:To further explore an efficient modified route for the shift from an antibacterial fluoroquinolone to an antitumor one,mono-Schiff bases 6a-6h related to ciprofloxacin C3 carbonylhydrazone and bis-Schiff bases 4a-4h corresponding to C3/C7 carbonylhydrazone/hydrazone attached on a skeleton of ciprofloquinolone were designed and synthesized,and their in vitro antitumor activity against CHO,HL60,L1210 cells and antibacterial activity against Staphylococcus aureus and Escherichia coli were also reported.
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