Jing Changling, Wang Cunfang, Yan Kai, Zhao Kedong, Sheng Guihua, Qu Dan, Niu Fang, Zhu Hailiang, You Zhonglu
Department of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, PR China.
School of Life Sciences, Shandong University of Technology, Zibo 255049, PR China.
Bioorg Med Chem. 2016 Jan 15;24(2):270-6. doi: 10.1016/j.bmc.2015.12.013. Epub 2015 Dec 8.
A series of new cobalt(III) complexes were prepared. They are [CoL(1)(py)3]·NO3 (1), [CoL(2)(bipy)(N3)]·CH3OH (2), [CoL(3)(HL(3))(N3)]·NO3 (3), and [CoL(4)(MeOH)(N3)] (4), where L(1), L(2), L(3) and L(4) are the deprotonated form of N'-(2-hydroxy-5-methoxybenzylidene)-3-methylbenzohydrazide, N'-(2-hydroxybenzylidene)-3-hydroxylbenzohydrazide, 2-[(2-dimethylaminoethylimino)methyl]-4-methylphenol, and N,N'-bis(5-methylsalicylidene)-o-phenylenediamine, respectively, py is pyridine, and bipy is 2,2'-bipyridine. The complexes were characterized by infrared and UV-Vis spectra, and single crystal X-ray diffraction. The Co atoms in the complexes are in octahedral coordination. Complexes 1 and 4 show effective urease inhibitory activities, with IC50 values of 4.27 and 0.35 μmol L(-1), respectively. Complex 2 has medium activity against urease, with IC50 value of 68.7 μmol L(-1). While complex 3 has no activity against urease. Molecular docking study of the complexes with Helicobacter pylori urease was performed.
制备了一系列新型钴(III)配合物。它们分别是[CoL(1)(py)3]·NO3(1)、[CoL(2)(bipy)(N3)]·CH3OH(2)、[CoL(3)(HL(3))(N3)]·NO3(3)和[CoL(4)(MeOH)(N3)](4),其中L(1)、L(2)、L(3)和L(4)分别是N'-(2-羟基-5-甲氧基苄叉基)-3-甲基苯甲酰肼、N'-(2-羟基苄叉基)-3-羟基苯甲酰肼、2-[(2-二甲基氨基乙基亚氨基)甲基]-4-甲基苯酚和N,N'-双(5-甲基水杨叉基)-邻苯二胺的去质子化形式,py是吡啶,bipy是2,2'-联吡啶。通过红外光谱、紫外可见光谱和单晶X射线衍射对配合物进行了表征。配合物中的钴原子呈八面体配位。配合物1和4表现出有效的脲酶抑制活性,IC50值分别为4.27和0.35 μmol L(-1)。配合物2对脲酶具有中等活性,IC50值为68.7 μmol L(-1)。而配合物3对脲酶没有活性。对这些配合物与幽门螺杆菌脲酶进行了分子对接研究。