New 2-Phenylthiazoles as Potential Sortase A Inhibitors: Synthesis, Biological Evaluation and Molecular Docking

被引:28
作者
Oniga, Smaranda Dafina [1 ]
Araniciu, Catalin [1 ]
Palage, Mariana Doina [1 ]
Popa, Marcela [2 ,3 ]
Chifiriuc, Mariana Carmen [2 ,3 ]
Marc, Gabriel [1 ]
Pirnau, Adrian [4 ]
Stoica, Cristina Ioana [1 ]
Lagoudis, Ioannis [1 ]
Dragoumis, Theodoros [1 ]
Oniga, Ovidiu [1 ]
机构
[1] Iuliu Hatieganu Univ Med & Pharm, Fac Pharm, 8 Victor Babes St, Cluj Napoca 400012, Romania
[2] Univ Bucharest, Fac Biol, Dept Microbiol, 1-3 Portocalelor St, Bucharest 60101, Romania
[3] Univ Bucharest, Res Inst, ICUB, 91-95 Independentei St, Bucharest 050095, Romania
[4] Natl Inst Res & Dev Isotop & Mol Technol, 67-103 Donat St, Cluj Napoca 400293, Romania
关键词
2-phenylthiazole; thiazole; antimicrobial; anti-biofilm activity; Sortase A inhibitor; enteroccocus; STAPHYLOCOCCUS-AUREUS SORTASE; GRAM-POSITIVE BACTERIA; ENTEROCOCCUS-FAECALIS; 3-DIMENSIONAL STRUCTURES; PROTEINS; DERIVATIVES; RECOGNITION; VALIDATION; RESISTANCE; INFECTION;
D O I
10.3390/molecules22111827
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
Sortase A inhibition is a well establish strategy for decreasing bacterial virulence by affecting numerous key processes that control biofilm formation, host cell entry, evasion and suppression of the immune response and acquisition of essential nutrients. A meta-analysis of structures known to act as Sortase A inhibitors provided the starting point for identifying a new potential scaffold. Based on this template a series of new potential Sortase A inhibitors, that contain the 2-phenylthiazole moiety, were synthesized. The physicochemical characterisation confirmed the identity of the proposed structures. Antibacterial activity evaluation showed that the new compounds have a reduced activity against bacterial cell viability. However, the compounds prevent biofilm formation at very low concentrations, especially in the case of E. faecalis. Molecular docking studies performed estimate that this is most likely due to the inhibition of Sortase A. The new compounds could be used as add-on therapies together with known antibacterial agents in order to combat multidrug-resistance enterococcal infections.
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页数:18
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