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首页> 外文期刊>Biological & pharmaceutical bulletin >Anti-Pseudomonas aeruginosa compound, 1,2,3,4-tetrahydro-1,3,5-triazine derivative, exerts its action by primarily targeting MreB
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Anti-Pseudomonas aeruginosa compound, 1,2,3,4-tetrahydro-1,3,5-triazine derivative, exerts its action by primarily targeting MreB

机译:铜绿假单胞菌(Pseudomonas aeruginosa)化合物1,2,3,4-四氢-1,3,5-三嗪衍生物通过主要靶向MreB发挥作用

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摘要

In order to find new anti-Pseudomonas agents, we carried out whole-cell based P. aeruginosa growth assay, and identified 1,2,3,4-tetrahydro-1,3,5- triazine (Compound A). This compound showed anti- Pseudomonas activity against wild as well as pumpless strain equally at a same concentration. Also, this compound was structurally very similar to A22, which is known to inhibit the bacterial actin-like protein MreB. By the analysis of resistant strains, the primary target of this compound in P. aeruginosa was definitely confirmed to be MreB. In addition, these compounds showed a bacteriostatic effect, and induced the morphology changes in P. aeruginosa from rod shape to sphere shape, which leads to be clinically favorable in terms of susceptibility to phagocytosis and release of endotoxin. These results display that Compound A is a very attractive compound which shows anti- P. aeruginosa activity based on inhibition of MreB without being affected by efflux pumps, and could provide a new step toward development of new promising anti- Pseudomonas agents, MreB inhibitors.
机译:为了找到新的抗假单胞菌药物,我们进行了基于全细胞的铜绿假单胞菌生长测定,并鉴定了1,2,3,4-四氢-1,3,5-三嗪(化合物A)。该化合物在相同浓度下对野生和无泵菌株均显示出抗假单胞菌活性。同样,该化合物在结构上与A22非常相似,已知它可以抑制细菌肌动蛋白样蛋白MreB。通过抗药性菌株的分析,该化合物在铜绿假单胞菌中的主要靶点肯定是MreB。另外,这些化合物显示出抑菌作用,并引起铜绿假单胞菌从杆状到球状的形态变化,就吞噬作用和内毒素释放的敏感性而言在临床上是有利的。这些结果表明化合物A是非常有吸引力的化合物,其基于对MreB的抑制而显示出抗铜绿假单胞菌的活性,而不受外排泵的影响,并且可以为开发新的有希望的抗假单胞菌剂MreB抑制剂提供新的步骤。

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