class='kwd-title'>Keywords: Urease inhibitors, U'/> A review on the development of urease inhibitors as antimicrobial agents against pathogenic bacteria
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A review on the development of urease inhibitors as antimicrobial agents against pathogenic bacteria

机译:脲酶抑制剂作为致病菌抗菌剂的研究进展

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摘要

class="kwd-title">Keywords: Urease inhibitors, Urea, Thiourea, Heterocycles, Phosphorated compounds class="head no_bottom_margin" id="ab010title">AbstractUreases are enzymes that hydrolyze urea into ammonium and carbon dioxide. They have received considerable attention due to their impacts on living organism health, since the urease activity in microorganisms, particularly in bacteria, are potential causes and/or factors contributing to the persistence of some pathogen infections. This review compiles examples of the most potent antiurease organic substances. Emphasis was given to systematic screening studies on the inhibitory activity of rationally designed series of compounds with the corresponding SAR considerations. Ureases of Canavalia ensiformis, the usual model in antiureolytic studies, are emphasized. Although the active site of this class of hydrolases is conserved among bacteria and vegetal ureases, the same is not observerd for allosteric site. Therefore, inhibitors acting by participating in interactions with the allosteric site are more susceptible to a potential lack of association among their inhibitory profile for different ureases. The information about the inhibitory activity of different classes of compounds can be usefull to guide the development of new urease inhibitors that may be used in future in small molecular therapy against pathogenic bacteria.
机译:<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> class =“ kwd-title”>关键字:脲酶抑制剂,尿素,硫脲,杂环,磷化合物 class =“ head no_bottom_margin” id = “ ab010title“>摘要尿素是将尿素水解成铵和二氧化碳的酶。由于它们对活生物体健康的影响,它们受到了相当大的关注,因为微生物(尤其是细菌)中的脲酶活性是导致某些病原体感染持续存在的潜在原因和/或因素。这篇综述汇编了最有效的抗脲酶有机物质的例子。重点是系统地筛选研究了合理设计的一系列化合物的抑制活性,并考虑了相应的SAR。强调了Canavalia ensiformis的尿素,这是抗尿素溶解研究中的常用模型。尽管这类水解酶的活性位点在细菌和植物脲酶之间是保守的,但对于别构位点却没有观察到。因此,通过参与与变构位点的相互作用而起作用的抑制剂更容易在其对不同脲酶的抑制谱之间缺乏关联。有关不同类别化合物抑制活性的信息可用于指导开发新的脲酶抑制剂,这些抑制剂将来可用于针对病原菌的小分子疗法。

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