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首页> 外文期刊>Chemistry Letters >20S Proteasome Inhibitory Activity of [N-(9-Anthracenylmethyl)-1,3-propanediamine] (2,2 '-Bipyridine) Palladium(II) Chloride
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20S Proteasome Inhibitory Activity of [N-(9-Anthracenylmethyl)-1,3-propanediamine] (2,2 '-Bipyridine) Palladium(II) Chloride

机译:20S蛋白酶体抑制活性[N-(9-蒽基甲基)-1,3-丙二胺](2,2'-β-吡啶)钯(II)氯化物

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摘要

The new palladium(II) complex, [Pd(bpy)(AtC3)](2+), where bpy = 2,2'-bipyridine and AtC3 = N-(9-anthracenylmethyl)-1,3-propanediamine, was synthesized and characterized. The crystal structure of [Pd(bpy)(AtC3)](2+) was determined. An intramolecular p-p stacking interaction was observed between anthracene and bipyridine. [Pd(bpy)(AtC3)](2+) exhibited 20S proteasome inhibitory activity. [Pd(bpy)(AtC3)](2+) also inhibited the proteolytic activity of cathepsin B, but not that of a-chymotripsin. Thus, [Pd(bpy)(AtC3)](2+) showed moderate selectivity for proteases. The binding mode of [Pd(bpy)(AtC3)](2+) to 20S proteasome was shown to be irreversible in a washout assay.
机译:综合新的钯(II)复合物[Pd(BPY)(ATC3)](2+),其中Bpy = 2,2'-Biphyridine和ATC3 = N-(9-蒽基甲基)-1,3-丙二胺。 并表征。 测定[Pd(BPY)(ATC3)](2+)的晶体结构。 在蒽和双吡啶之间观察到分子内P-P堆叠相互作用。 [Pd(BPY)(ATC3)](2+)表现出20S蛋白酶体抑制活性。 [Pd(BPY)(ATC3)](2+)还抑制了组织蛋白酶B的蛋白水解活性,但不是A-ChyMotripsin的蛋白水解活性。 因此,[Pd(BPY)(ATC3)](2+)显示出适度的蛋白酶选择性。 [Pd(BPY)(ATC3)](2+)至20s蛋白酶体的结合模式显示在冲洗测定中是不可逆的。

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