A Nine-Coordinated Bismuth(III) Complex Derived from Pentadentate 2,6-Diacetylpyridine Bis(4N-methylthiosemicarbazone): Crystal Structure and Both in Vitro and in Vivo Biological Evaluation

被引:75
作者
Li, Ming-Xue [1 ]
Yang, Min [1 ]
Niu, Jing-Yang [1 ]
Zhang, Li-Zhi [1 ]
Xie, Song-Qiang [2 ]
机构
[1] Henan Univ, Polyoxometalates Chem Key Lab Henan Prov, Coll Chem & Chem Engn, Inst Mol & Crystal Engn, Kaifeng 475004, Peoples R China
[2] Henan Univ, Inst Biol Chem, Kaifeng 475004, Peoples R China
基金
中国国家自然科学基金;
关键词
ANTIMICROBIAL ACTIVITIES; DIORGANOTIN(IV) COMPLEXES; COORDINATION CHEMISTRY; BIOINORGANIC CHEMISTRY; SEMICARBAZONE LIGANDS; NICKEL(II) COMPLEXES; SARS CORONAVIRUS; ZN(II) COMPLEXES; METAL-COMPLEXES; FOOD SAMPLES;
D O I
10.1021/ic301959z
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Up to now, bismuth(III) complexes with thiosemicarbazones have been comparatively rare. Few in vivo biological studies have been carried out in comparison to the plentiful in vitro data. Here, an interesting nine-coordinated bismuth(III) complex, [Bi(H2L)(NO3)(2)]NO3 [1; H2L = 2,6-diacetylpyridine bis(N-4-methylthiosemicarbazone)], has been synthesized and structurally characterized. The analytical data reveal the formation of 1:1 (metal/ligand) stoichiometry. In vitro biological studies have indicated that the bismuth complex 1 has shown much higher antibacterial and anticancer activities than its parent ligand, especially with MIC = 10.66 mu M against Bacillus cereus and Salmonella typhimurium and IC50 = 26.8 mu M against K562 leukemia cells, respectively. More importantly, it also evidently inhibits H22 xenograft tumor growth on tumor-bearing mice (10 mg/kg; inhibitory rate = 61.6%). These results indicate that coordination to bismuth(III) might be an interesting strategy in the discovery of new anticancer drug candidates.
引用
收藏
页码:12521 / 12526
页数:6
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