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首页> 外文期刊>Journal of Molecular Structure >Synthesis, crystal structures, fluorescence and xanthine oxidase inhibitory activity of pyrazole-based 1,3,4-oxadiazole derivatives
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Synthesis, crystal structures, fluorescence and xanthine oxidase inhibitory activity of pyrazole-based 1,3,4-oxadiazole derivatives

机译:吡唑基1,3,4-恶二唑衍生物的合成,晶体结构,荧光和黄嘌呤氧化酶抑制活性

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A series of pyrazole-based 1,3,4-oxadiazole derivatives were rationally designed and synthesized in good yields by following a convenient route. All the newly synthesized molecules were fully characterized by IR, H-1 NMR and elemental analysis. Eight compounds were structurally determined by single crystal Xray diffraction analysis. The fluorescence properties of all the compounds were investigated in dimethyl sulfoxide media. In addition, these newly synthesized compounds were evaluated for in vitro inhibitory activity against commercial enzyme xanthine oxidase (XO) by measuring the formation of uric acid from xanthine. Among the compounds synthesized and tested, 3d and 3e were found to be moderate inhibitory activity against commercial XO with IC50 = 72.4 mu M and 75.6 mu M. The studies gave a new insight in further optimization of pyrazole-based 1,3,4-oxadiazole derivatives with excellent fluorescence properties and XO inhibitory activity. (C) 2015 Elsevier B.V. All rights reserved.
机译:合理设计了一系列吡唑基1,3,4-恶二唑衍生物,并通过一条方便的途径以高收率合成了这些衍生物。所有新合成的分子均通过IR,H-1 NMR和元素分析充分表征。通过单晶X射线衍射分析在结构上确定了八种化合物。在二甲基亚砜介质中研究了所有化合物的荧光性质。此外,通过测量黄嘌呤中尿酸的形成,评估了这些新合成的化合物对商业化酶黄嘌呤氧化酶(XO)的体外抑制活性。在合成和测试的化合物中,发现3d和3e具有对商业XO的中等抑制活性,IC50 = 72.4μM和75.6μM。该研究为进一步优化基于吡唑的1,3,4-提供了新的见解。恶二唑衍生物具有出色的荧光性质和XO抑制活性。 (C)2015 Elsevier B.V.保留所有权利。

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