首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Novel phenyl(thio)ureas bearing (thio)oxothiazoline group as potential BACE-1 inhibitors: synthesis and biological evaluation
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Novel phenyl(thio)ureas bearing (thio)oxothiazoline group as potential BACE-1 inhibitors: synthesis and biological evaluation

机译:具有潜在的BACE-1抑制剂的新型带有(硫代)氧噻唑啉基的苯基(硫代)脲:合成和生物学评估

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Abstract We report the synthesis and the β-site amyloid precursor protein cleaving enzyme-1 inhibitory properties of novel phenyl(thio)ureas bearing 2-(thio)oxothiazoline derivatives. A library of analogues was prepared according to specific synthetic schemes and the inhibitory activity was monitored using a fluorescence resonance energy transfer assay. Several analogues show potent inhibitory activities ranging between 1 and 0.01 μM and the activity is related to the NH acidity of the (thio)urea motif. Our results illustrate once again the close relationship between molecular recognition, complexation of the active site in enzymatic system, and organocatalysis utilizing explicit hydrogen bonding.
机译:摘要我们报道了带有2-(硫代)氧噻唑啉衍生物的新型苯基(硫代)脲的合成及其β位淀粉样蛋白前体蛋白裂解酶-1的抑制特性。根据特定的合成方案制备类似物文库,并使用荧光共振能量转移测定法监测抑制活性。几种类似物显示出有效的抑制活性,范围在1至0.01μM之间,并且该活性与(硫代)脲基序的NH酸度有关。我们的结果再次说明了分子识别,酶系统中活性位点的络合和利用显式氢键的有机催化之间的密切关系。

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