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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Design and synthesis of biotinylated Hexylselen as a probe to identify KGA allosteric inhibitors by a convenient biomolecular interaction assay
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Design and synthesis of biotinylated Hexylselen as a probe to identify KGA allosteric inhibitors by a convenient biomolecular interaction assay

机译:用方便的生物分子相互作用测定设计和合成鉴定KGA变构抑制剂的探针

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Hexylselen is a novel submicromolar dual KGA/GDH inhibitor, which demonstrates potent inhibition of cancer cells with minimal toxicity. To further investigation its mechanism of action, we designed and synthesized its biotinylated derivative 2 as a novel probe. From commercially available starting material, 2 was obtained in 6 steps with 13.4% overall yield. It is notable that this practical synthetic route give a template for the preparation of unsymmetrical di-benzo[d] [1,2]selenazol-3(2H)-ones. Based on probe 2, we developed a novel biomolecular interaction assay for convenient and reliable test of KGA allosteric inhibitors and confirmed that hexylselen as an allosteric inhibitor of KGA sharing the same binding pocket with BPTES but not with Ebselen via competitive experiments.
机译:己硅硒是一种新型亚微粒摩尔双KGA / GDH抑制剂,其表明毒性最小的癌细胞有效抑制。 进一步调查其作用机制,我们设计并合成了其生物素化衍生物2作为新型探针。 从市售的原料,在6个步骤中获得2个,总产量为13.4%。 值得注意的是,这种实际的合成途径给出了制备非对称二苯并[D] [1,2]硒唑-3(2H)酮的模板。 基于探针2,我们开发了一种新的生物分子相互作用测定,用于kGa变构抑制剂的方便和可靠性测试,并确认己基作为KGA的变构抑制剂与BPTE共享相同的结合口袋,但不通过竞争实验与EBSELEN相同。

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