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首页> 外文期刊>Pharmaceutical Chemistry Journal >Antioxidant Activity of Ruthenium(Ii) Complexes Containing Tridentate Triamines and Their Capability to Inhibit Xanthine Oxidase
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Antioxidant Activity of Ruthenium(Ii) Complexes Containing Tridentate Triamines and Their Capability to Inhibit Xanthine Oxidase

机译:含钌(II)络合物的抗氧化活性含有三叶三胺及其抑制黄嘌呤氧化酶的能力

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摘要

Biological activities of organoruthenium complexes [chloro [N,N '-[(2,6-pyridinediyl-kappa N) diethylidyne] bis-[benzenamine-kappa N]] [N-[(2-pyridinyl-kappa N) methylene] benzenesulfonamide-kappa N] ruthenium(II)] chloride (Cmplx 1), [chloro [2,2 '-(2,6-pyridinediyl-kappa N) bis [1H-benzimidazole-kappa N-3]][N-[(2-pyridinyl-kappa N) methylene] benzenesulfonamide-kappa N] ruthenium(II)] chloride (Cmplx 2), and [chloro[2,6-di(1H-pyrazol-3-yl-kappa N-2) pyridine-kappa N] [N-[(2-pyridinyl-kappa N) methylene] [benzenesulfonamide-kappa N] ruthenium(II)] chloride (Cmplx 3) have been studies. The compounds were tested for in vitro biological activity on test models including 2,2-diphenyl-1-picryl-hydrazyl (DPPH) reducing power, superoxide anion radical-scavenging activity, and lipid peroxidation activity by ferric thiocyanate. It is established that Cmplx 2 with benzimidazole ligand displays significant xanthine oxidase inhibitory activity (IC50 = 53.80 +/- 2.69 mu M), DPPH free radical scavenging activity (79.49 +/- 1.59), and superoxide anion radical scavenging activity (75.73 +/- 2.85%). The coordination of benzenamine and benzenesulfanoamine ligands reduces lipid peroxidation as observed in the case of Cmplx 1 (87.17 +/- 3.88%) and the higher reducing power of Cmplx 1 obtained at all concentrations. It was concluded from the test results that organoruthenium complexes showed much better antioxidant activity than expected.
机译:有机丁烯络合物的生物活性[氯[N,N' - [(2,6-吡啶啉基-κNN)二乙基苯基]双 - [苯甲酰氨基-κN] [N - [(2-吡啶基-Kappa N)亚甲基]苯磺胺酰胺-Kappa n]钌(II)]氯化物(CMPLX 1),[氯[2,2' - (2,6-吡啶啉基-Kappa n)双[1H-苯并咪唑-Kappa n-3]] [n - [( 2-吡啶基-κN)亚甲基苯磺酰胺-Kappa N]钌(II)]氯化物(CMPLX 2),和氯化酰氯[2,6-二(1H-吡唑-3-基-Kappa N-2)吡啶 - Kappa N] [N - [(2-吡啶基-Kappa n)亚甲基] [苯磺酰胺-Kappa N]钌(II)]氯化物(CMPLX 3)已经研究。通过铁硫代氰酸酯测试在试验模型上进行体外生物活性的体外生物活性,通过铁硫氰酸酯对等试验模型进行体外生物活性。建立CMPLX 2与苯并咪唑配体显示出显着的黄嘌呤氧化酶抑制活性(IC50 = 53.80 +/-2.69μm),DpPH自由基清除活性(79.49 +/- 1.59)和超氧化物阴离子激进的清除活性(75.73 + / - 2.85%)。本zenamine和苯磺酰胺配体的配位降低了在CMPLX 1(87.17 +/- 3.88%)的情况下观察到的脂质过氧化,并且在所有浓度下获得的CMPLX 1的较高减小功率。从测试结果中得出结论,使得有机素烯核复合物显示比预期更好的抗氧化活性。

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