Ly Ta Ngoc, Lan Le My, Tsai Ming-Yu, Chen Yun-Wen, Hung Hsin-Yi
The University of Da Nang-University of Science and Technology, Danang 550000, Vietnam.
School of Pharmacy and Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, Tainan 701, Taiwan.
ACS Omega. 2024 Sep 20;9(39):40897-40906. doi: 10.1021/acsomega.4c06115. eCollection 2024 Oct 1.
The incidence of treatment failure due to multidrug-resistant pathogens elevated over the years; the rate is much higher than new antibiotic drug discovery. Therefore, bromophenol derivatives as potential antibacterial agents on and MRSA were explored in this research via integrating chemistry, microbiology, and pharmacology to address significant knowledge gaps pertaining to the antibacterial activity of bromophenols based on their functional groups. Surprisingly, a simple molecule, 3-bromo-2,6-dihydroxyacetophenone (), exhibited good anti- activity and even MRSA, a drug-resistant strain. In addition, compound also inhibited a common resistant pathway of pathogens, biofilm formation of and MRSA. Moreover, the therapeutic index of is up to 598, which can be viewed as highly selective and having low toxicity to human HEK-293 cells. Although these compounds displayed less effectiveness for the Gram-negative bacterium, , they still manifested some effects on the virulence properties of , such as biofilm formation, pyocyanin production, and swarming motility. analyses of the structure-activity relationship as well as ADMET properties were discussed in the end. This study shed some light on the antibacterial activities of bromophenols.
多年来,由多重耐药病原体导致的治疗失败发生率不断上升;这一比率远高于新抗生素药物的发现率。因此,本研究通过整合化学、微生物学和药理学,探索了溴酚衍生物作为潜在的抗[具体细菌名称未给出]和耐甲氧西林金黄色葡萄球菌(MRSA)的抗菌剂,以填补基于溴酚官能团的抗菌活性方面的重大知识空白。令人惊讶的是,一个简单的分子,3 - 溴 - 2,6 - 二羟基苯乙酮([具体编号未给出]),对[具体细菌名称未给出]甚至对耐药菌株MRSA都表现出良好的抗菌活性。此外,化合物[具体编号未给出]还抑制了病原体的一种常见耐药途径,即[具体细菌名称未给出]和MRSA的生物膜形成。而且,[具体编号未给出]的治疗指数高达598,可被视为对人类HEK - 293细胞具有高度选择性且低毒性。尽管这些化合物对革兰氏阴性菌[具体细菌名称未给出]的效果较差,但它们对[具体细菌名称未给出]的毒力特性,如生物膜形成、绿脓菌素产生和群集运动性,仍表现出一些影响。最后讨论了结构 - 活性关系以及药物代谢动力学、药物代谢和毒性性质(ADMET)的分析。这项研究为溴酚的抗菌活性提供了一些启示。