大肠杆菌RecA atp酶活性的新型抑制剂。

Jonathan Z Sexton, Tim J Wigle, Qingping He, Mark A Hughes, Ginger R Smith, Scott F Singleton, Alfred L Williams, Li-An Yeh
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引用次数: 51

摘要

细菌RecA蛋白已被认为是细菌药物靶点,而不是抗菌靶点,而是具有抑制细菌获得耐药性机制的潜在佐剂靶点。为了鉴定抑制RecA/ssDNA核蛋白细丝形成的小分子,我们采用磷酸甘酸蓝atp酶测定法进行高通量筛选,以确定RecA atp酶对33,600种化合物的活性,这些化合物是35万种不同结构的精选代表。四种不同的化学型在40个验证命中。目前正在进行SAR和进一步的化学合成以优化这组抑制剂作为抗菌佐剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Novel Inhibitors of E. coli RecA ATPase Activity.

The bacterial RecA protein has been implicated as a bacterial drug target not as an antimicrobial target, but as an adjuvant target with the potential to suppress the mechanism by which bacteria gain drug resistance. In order to identify small molecules that inhibit RecA/ssDNA nucleoprotein filament formation, we have adapted the phosphomolybdate-blue ATPase assay for high throughput screening to determine RecA ATPase activity against a library of 33,600 compounds, which is a selected representation of diverse structure of 350,000. Four distinct chemotypes were represented among the 40 validated hits. SAR and further chemical synthesis is underway to optimize this set of inhibitors to be used as antimicrobial adjuvant agents.

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