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Synthesis, structure and biological properties of benzimidazole-based Cu(II)/Zn(II) complexes

机译:基于苯并咪唑基Cu(II)/ Zn(II)复合物的合成,结构和生物学性质

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Three new complexes formulated as [Cu(mbmb)(2)Cl-2] (1), [Cu(mbmb)(2)(NO3)(2)] (2), and [Zn(mbmb)(2)Cl-2] (3) (mbmb = 1-[(2-methyl-1H-benzoimidazol-1-yl)methyl]-1H-benzotriazole) have been synthesized and characterized. Complexes 1-3 showed mononuclear structures and the central metal ions of complexes 1-3 exhibited a four-coordinated environment. We evaluated the antioxidant activity against DPPH and antidiabetic activity against alpha-amylase of complexes 1-3 and ligand (mbmb) in vitro. The results of DPPH free radical scavenging assay showed that complexes 1 and 2 exhibited higher antioxidant activity among the synthesized compounds and their IC50 values were 43.72 mu g/mL and 43.76 mu g/mL, respectively. The IC50 values in vitro antidiabetic studies of complex 1 (0.74 mg/mL) and complex 2 (1.00 mg/mL) were much smaller than those of standard acarbose (2.34 mg/mL) and the ligand mbmb (39.87 mg/mL), which showed effective inhibition on alpha-amylase. Additionally, the solid-state fluorescent properties of these three complexes and ligand mbmb were investigated at room temperature.
机译:配制为[Cu(MBMB)(2)(2)Cl-2](1),[Cu(MBMB)(2)(2)(2),和[Zn(MBMB)(2)Cl的三种新复合物已经合成并表征了-2](3)(MBMB = 1 - [(2-甲基-1H-苯并咪唑-1-基)甲基] -1H-苯并三唑)。复合物1-3显示单核结构,复合物的中央金属离子1-3表现出四种协调的环境。我们在体外评估对络合物1-3和配体(MBMB)的α-淀粉酶的DPPH和抗糖尿病活性的抗氧化活性。 DPPH自由基清除测定的结果表明,络合物1和2在合成化合物中表现出更高的抗氧化活性,其IC 50值分别为43.72μg和43.76μg/ ml。复合物1(0.74mg / ml)和复合物2(1.00mg / ml)的体外抗糖分能研究的IC 50值远小于标准氨基糖(2.34mg / ml)和配体MBMB(39.87mg / ml),这在α-淀粉酶上显示出有效的抑制作用。另外,在室温下研究了这三种配合物和配体MBMB的固态荧光特性。

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