Rauf Muhammad Khawar, Yaseen Samad, Badshah Amin, Zaib Sumera, Arshad Raffia, Tahir Muhammad Nawaz, Iqbal Jamshed
Department of Chemistry, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
J Biol Inorg Chem. 2015 Apr;20(3):541-54. doi: 10.1007/s00775-015-1239-5. Epub 2015 Jan 22.
A series of N,N,N'-trisubstituted thioureas (1-12) and their Ni(II) complexes (1a-12a) were synthesized and characterized by multinuclear ((1)H and (13)C) NMR, FT-IR spectroscopy and LC-MS techniques in combination with elemental analysis. The crystal structures of both ligands and Ni(II) chelates of type Ni(L-O, S)2 were determined by single crystal X-ray diffraction analysis. All the complexes were adopted to have square planar geometry, where the N,N,N'-trisubstituted thioureas showed bidentate mode of coordination at nickel centre through oxygen and sulfur atoms. The synthesized complexes were screened for potential inhibitors of Jack bean urease. Compounds 1a and 3a were observed as most potent inhibitors of urease exhibiting IC50 values of 1.17 ± 0.12 and 1.19 ± 0.41 µM, respectively. Cytotoxicity assay on lung carcinoma (H-157) and kidney fibroblast (BHK-21) cell showed that compounds were significant anticancer agents. Additionally, the complexes were tested against Leishmania major and found to be potent antileishmanial agents.
合成了一系列N,N,N'-三取代硫脲(1-12)及其镍(II)配合物(1a-12a),并通过多核((1)H和(13)C)核磁共振、傅里叶变换红外光谱和液相色谱-质谱技术结合元素分析对其进行了表征。通过单晶X射线衍射分析确定了Ni(L-O,S)2型配体和镍(II)螯合物的晶体结构。所有配合物均采用平面正方形几何结构,其中N,N,N'-三取代硫脲通过氧和硫原子在镍中心呈现双齿配位模式。对合成的配合物进行了刀豆脲酶潜在抑制剂的筛选。观察到化合物1a和3a是脲酶最有效的抑制剂,其IC50值分别为1.17±0.12和1.19±0.41μM。对肺癌(H-157)和肾成纤维细胞(BHK-21)的细胞毒性试验表明,这些化合物是显著的抗癌剂。此外,对这些配合物进行了抗硕大利什曼原虫测试,发现它们是有效的抗利什曼原虫剂。