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一种针对 细胞壁生物合成的芳基砜酰胺。

An arylsulfonamide that targets cell wall biosynthesis in .

机构信息

Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, Washington, USA.

Lgenia, Fortville, Indiana, USA.

出版信息

Antimicrob Agents Chemother. 2024 Nov 6;68(11):e0103724. doi: 10.1128/aac.01037-24. Epub 2024 Sep 26.

Abstract

We investigated the mechanism of action of an arylsulfonamide with whole-cell activity against . We newly synthesized the molecule and confirmed it had activity against both extracellular and intracellular bacilli. The molecule had some activity against HepG2 cells but maintained some selectivity. Bacterial cytological profiling suggested that the mechanism of action was via disruption of cell wall synthesis, with similarities to an inhibitor of the mycolic acid exporter MmpL3. The compound induced expression from the IniB promoter and caused a boost in ATP production but did not induce reactive oxygen species. A mutation in MmpL3 (S591I) led to low-level resistance. Taken together, these data confirm the molecule targets cell wall biosynthesis with MmpL3 as the most probable target.

摘要

我们研究了一种具有抗 全细胞活性的芳基磺胺的作用机制。我们新合成了该分子,并证实其对胞外和胞内分枝杆菌均有活性。该分子对 HepG2 细胞有一定的活性,但保持了一定的选择性。细菌细胞形态学分析表明,其作用机制是通过破坏细胞壁合成,与分枝杆菌酸外排蛋白 MmpL3 的抑制剂相似。该化合物诱导 IniB 启动子表达并增加 ATP 产生,但不诱导活性氧的产生。MmpL3(S591I)突变导致低水平耐药。综上所述,这些数据证实该分子以 MmpL3 为最可能的靶标,靶向细胞壁生物合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4109/11539219/e4e1f226ef82/aac.01037-24.f001.jpg

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