A Novel Class of Cationic and Non-Peptidic Small Molecules as Hits for the Development of Antimicrobial Agents

被引:7
作者
Jimenez, Aranza [1 ,4 ]
Garcia, Pablo [2 ]
de la Puente, Sofia [1 ]
Madrona, Andres [1 ,5 ]
Jose Camarasa, Maria [1 ]
Perez-Perez, Maria-Jesus [1 ]
Quintela, Jose-Carlos [3 ]
Garcia-del Portillo, Francisco [2 ]
San-Felix, Ana [1 ]
机构
[1] CSIC, Inst Quim Med, Juan Cierva 3, E-28006 Madrid, Spain
[2] CSIC, CNB, Lab Patogenos Bacterianos Intracelulares, Darwin 3, Madrid 28049, Spain
[3] Natac Biotech SL, Parque Cient Madrid,Campus Cantoblanco, Madrid 28049, Spain
[4] Agencia Espanola Medicamentos & Prod Sanitario, Campezo 1,Edificio 8, Madrid 28022, Spain
[5] Novartis Farmaceut SA, Gran Via Corts Catalanes 764, Barcelona 08013, Spain
来源
MOLECULES | 2018年 / 23卷 / 07期
关键词
antimicrobial agents; antibiotic resistance; antimicrobial peptides; HOST-DEFENSE PEPTIDES; UNITED-STATES; RESISTANCE; MECHANISMS;
D O I
10.3390/molecules23071513
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cationic and non-peptide small molecules containing a total of six positive charges arranged on one side and a long aliphatic tail on the other have been synthesized and tested against Gram-positive and Gram-negative bacteria. The positive charges have been contributed by two aminophenol residues. These molecules have showed remarkable antimicrobial activity against Gram-positive bacteria including multidrug-resistant strains. Our structure-activity relationship studies demonstrated the importance of the length and flexibility of the hydrophobic tail for the antimicrobial activity. Importantly, these compounds are non-toxic to eukaryotic cells at the concentration affecting growth in bacteria, reflecting an acceptable margin of safety. The small size and easy synthetic accessibility of our molecules can be of interest for the further development of novel antimicrobials against Gram-positive bacterial pathogens, including multidrug-resistant strains.
引用
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页数:18
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