New Chlorophenyl Dioxo-Imidazolidines for Bacterial Biofilm

IF 3.5 4区 医学 Q2 CHEMISTRY, MEDICINAL
Shanmugha Samy, Manikandan Alagumuthu, Ooha Dharani Yalamaddi, Milind Shrinivas Dangate
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引用次数: 0

Abstract

Biofilm is a “growing” problem and needs effective remedial agents. Here we report novel methyl 4-((4-(4-chlorophenyl)-2,5-dioxoimidazolidin-1-yl) methyl) benzoate derivatives (5a-l) as antibiofilm and antimicrobial agents evaluated with both in silico and in vitro techniques. When it comes to Gram-positive bacterial strains like Staphylococcus aureus (MTCC 737), MRSA and Streptococcus pneumoniae (MTCC 1936), and Gram-negative bacterial strains like Pseudomonas aeruginosa (MTCC 424) and Escherichia coli (MTCC 443), the minimum inhibitory concentration (MIC), minimum biofilm inhibition concentration (MBIC), and anti-biofilm activity were measured. Out of all the compounds (5a-l), 5b and 5d showed no toxicity to mammalian cells and were equally active against various Gram-positive and Gram-negative bacteria at low concentrations (MIC: 0.1–9.5 µg/mL). Compounds 5b and 5d were also validated for the DNA gyrase inhibition potential as an antimicrobial mechanism of action in vitro. These compounds showed high level DNA gyrase inhibition potentials (IC50 0.025 µM, ≥ 98 relative % activity and 0.24 µM, ≥ 94 relative % activity respectively. In the end, we have identified 5b and 5d as most effective among 5a-l and are considered for further preclinical studies.

用于细菌生物膜的新型氯苯二氧咪唑烷类化合物
生物膜是一个“日益严重”的问题,需要有效的补救剂。在这里,我们报告了新的甲基4-((4-(4-氯苯基)-2,5-二氧基咪唑烷-1-基)甲基)苯甲酸酯衍生物(5a-l)作为抗生素膜和抗菌剂,用硅和体外技术进行了评估。测定革兰氏阳性菌株如金黄色葡萄球菌(MTCC 737)、MRSA和肺炎链球菌(MTCC 1936),革兰氏阴性菌株如铜绿假单胞菌(MTCC 424)和大肠埃希菌(MTCC 443)的最小抑菌浓度(MIC)、最小生物膜抑制浓度(MBIC)和抗生物膜活性。在所有化合物(5a-l)中,5b和5d对哺乳动物细胞没有毒性,并且在低浓度(MIC: 0.1-9.5µg/mL)下对各种革兰氏阳性和革兰氏阴性细菌具有相同的活性。化合物5b和5d在体外也被证实具有抑制DNA回转酶的作用机制。这些化合物显示出高水平的DNA回旋酶抑制潜力(IC50分别为0.025µM,≥98相对%活性和0.24µM,≥94相对%活性)。最后,我们确定5b和5d是5a-l中最有效的,并考虑进行进一步的临床前研究。
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来源期刊
CiteScore
6.40
自引率
2.60%
发文量
104
审稿时长
6-12 weeks
期刊介绍: Drug Development Research focuses on research topics related to the discovery and development of new therapeutic entities. The journal publishes original research articles on medicinal chemistry, pharmacology, biotechnology and biopharmaceuticals, toxicology, and drug delivery, formulation, and pharmacokinetics. The journal welcomes manuscripts on new compounds and technologies in all areas focused on human therapeutics, as well as global management, health care policy, and regulatory issues involving the drug discovery and development process. In addition to full-length articles, Drug Development Research publishes Brief Reports on important and timely new research findings, as well as in-depth review articles. The journal also features periodic special thematic issues devoted to specific compound classes, new technologies, and broad aspects of drug discovery and development.
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