Targeting the Bacterial Membrane with a New Polycyclic Privileged Structure: A Powerful Tool To Face Staphylococcus aureus Infections

被引:11
作者
Bonvicini, Francesca [1 ]
Manet, Ilse [2 ]
Belluti, Federica [3 ]
Gobbi, Silvia [3 ]
Rampa, Angela [3 ]
Gentilomi, Giovanna Angela [1 ,4 ]
Bisi, Alessandra [3 ]
机构
[1] Univ Bologna, Dept Pharm & Biotechnol, Alma Mater Studiorum, Via Massarenti 9, I-40138 Bologna, Italy
[2] CNR, Natl Res Council, Inst Organ Synth & Photoreact, ISOF, Via Piero Gobetti 101, I-40129 Bologna, Italy
[3] Univ Bologna, Dept Pharm & Biotechnol, Alma Mater Studiorum, Via Belmeloro 6, I-40126 Bologna, Italy
[4] Univ Bologna, St Orsola Malpighi Hosp, Unit Microbiol, Via Massarenti 9, I-40138 Bologna, Italy
来源
ACS INFECTIOUS DISEASES | 2019年 / 5卷 / 09期
关键词
anthracene-maleimide-based compounds; Staphylococcus aureus; membrane-disrupting activity; clinical strains; antibiotic resistance; PHYSICOCHEMICAL PROPERTIES; ANTIBACTERIAL COMPOUNDS; DRUG DISCOVERY; MECHANISMS; BIOFILM;
D O I
10.1021/acsinfecdis.9b00072
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this paper, a small series of anthracene-maleimide-based compounds was prepared and evaluated to assess the antimicrobial potential of this polycyclic core, a scaffold previously unexplored for new antibiotic development. Some of the new compounds showed appreciable anti-Staphylococcus aureus activity, together with good safety profiles. In particular, compound 13 proved to be the most promising of the series, showing remarkable antimicrobial activity toward planktonic and sessile bacterial cells within a mature preformed biofilm. The mechanism of action seems to be related to the ability of this compound to interfere with bacterial membrane functionality, probably through the targeting of key enzymes responsible for membrane redox homeostasis and energy production. The data reported confirm the ability of this polycyclic nucleus to behave as a new "privileged structure", suitable to be further exploited in the antimicrobial field.
引用
收藏
页码:1524 / 1534
页数:21
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