化学
钴
配体(生物化学)
过渡金属
铜
锌
立体化学
结晶学
对接(动物)
晶体结构
金属
配位复合体
镍
无机化学
有机化学
生物化学
受体
护理部
催化作用
医学
作者
Vinayak Kamat,Dhoolesh G. Kokare,Krishna Naik,Avinash Kotian,S. Naveen,Sheshagiri R. Dixit,N.K. Lokanath,Sangeeta B. Joshi,Vidyanand K. Revankar
出处
期刊:Polyhedron
[Elsevier]
日期:2017-02-21
卷期号:127: 225-237
被引量:11
标识
DOI:10.1016/j.poly.2017.02.010
摘要
Transition metal coordination complexes of Co(II), Ni(II), Cu(II) and Zn(II) with a newly designed ligand, 2-(2-(1H-benzo[d]imidazol-2-yl)hydrazono)propan-1-ol have been synthesized and characterized using various spectro-analytical techniques. The molecular structures of Co(II), Cu(II) and Zn(II) complexes are determined by single-crystal X-ray diffraction method. The metal to ligand stoichiometry has been found to be 1:2 in the case of Cobalt(II), Nickel(II) and Zinc(II) whereas 1:1 in the case of Copper(II) complex. The newly synthesized ligand and complexes have been assessed for their growth inhibiting potencies against H37Rv strain of Mycobacterium tuberculosis. The copper and cobalt complexes have emerged to be potent in vitro growth inhibitors of H37Rv. All the complexes are inhibiting the growth of other tested common microbial flora to a significantly lesser extent, making them selective towards H37Rv in the preliminary analysis. The consensus scores obtained by the docking studies of the molecules to the target protein enoyl acyl carrier protein reductase of M. tuberculosis H37Rv are in good agreement with the obtained MIC values.
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