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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and mechanistic studies of diketo acids and their bioisosteres as potential antibacterial agents
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Synthesis and mechanistic studies of diketo acids and their bioisosteres as potential antibacterial agents

机译:Diketo酸及其生物化剂作为潜在抗菌剂的合成与机械研究

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摘要

A series of diketo esters and their pertinent bioisosteres were designed and synthesized as potent antibacterial agents by targeting methionine amino peptidases (MetAPs). In the biochemical assay against purified MetAPs from Streptococcus pneumoniae (SpMetAPla), Mycobacterium tuberculosis (MtMetAP1c), Enterococcus faecalis (EfMetAPla) and human (HsMetAP1b), compounds 3a, 4a and 5a showed more than 85% inhibition of all the tested MetAPs at 100 p.M concentration. Compounds 4a and 5a also exhibited antibacterial potential with MIC values 62.514/mL (S. pneumoniae), 31.25 g/mL (E. faecalis), 62.5 g/mL (Escherichia coli) and 62.5 ggirnL (S. pneumoniae), 62.5 g/mL (E. coli), respectively. Moreover, 5a also significantly inhibited the growth of multidrug resistant E. coli strains at 512 g/ mL conc., while showing no cytotoxic effect towards healthy CHO cells and thus being selected. Growth kinetics study showed significant inhibition of bacterial growth when treated with different conc. of 5a. TEM analysis also displayed vital damage to bacterial cells by 5a at MIC conc. Moreover, significant inhibition of biofilm formation was observed in bacterial cells treated with MIC conc. of 5a as visualized by SEM micrographs. Interestingly, 5a did not cause an alteration in the hemocyte density in Galleria mellonella larvae which is considered in vivo model for antimicrobial studies and was non-toxic up to a conc. of 2.5 mg/mL. (C) 2018 Elsevier Masson SAS. All rights reserved.
机译:通过靶向甲硫氨酸氨基肽酶(MOTAPS)设计并合成一系列Diketo酯及其相关的生物蛋白剂作为有效的抗菌剂。在生化测定中,来自链球菌(Spetapla),结核病(MTMETAP1C),肠球菌(EFMETAPLA)和人(HSEMEDAP1B),化合物3a,4a和5a的纯化测定,表明,在100时显示出所有测试的标记的抑制超过85% PM浓度。化合物4a和5a还表现出抗菌电位,具有MIC值62.514 / ml(S.肺炎),31.25g / ml(大肠杆菌),62.5g / ml(大肠杆菌)和62.5ggirn1(S.肺炎),62.5g /分别为m1(大肠杆菌)。此外,在512g / ml浓度下,5a也显着抑制多药物抗性大肠杆菌菌株的生长,同时显示对健康CHO细胞没有细胞毒性作用,从而选择。生长动力学研究表明用不同浓度处理时对细菌生长的显着抑制。 5a。 TEM分析在MIC COC中,在5A中对细菌细胞的致力损伤。此外,在用麦克风浓度处理的细菌细胞中观察到生物膜形成的显着抑制。由SEM显微照片可视化5A。有趣的是,5A没有引起血细胞密度的血细胞密度的改变,其在体内抗微生物研究中考虑了体内模型,并且无毒地浓缩。 2.5 mg / ml。 (c)2018年Elsevier Masson SAS。版权所有。

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