Isatin Bis-Indole and Bis-Imidazothiazole Hybrids: Synthesis and Antimicrobial Activity

被引:8
|
作者
Bonvicini, Francesca [1 ]
Locatelli, Alessandra [2 ]
Morigi, Rita [2 ]
Leoni, Alberto [2 ]
Gentilomi, Giovanna Angela [1 ,3 ]
机构
[1] Alma Mater Studiorum Univ Bologna, Dept Pharm & Biotechnol, Via Massarenti 9, I-40138 Bologna, Italy
[2] Alma Mater Studiorum Univ Bologna, Dept Pharm & Biotechnol, Via Belmeloro 6, I-40126 Bologna, Italy
[3] IRCCS Azienda Osped Univ Bologna, Div Microbiol, Via Massarenti 9, I-40138 Bologna, Italy
来源
MOLECULES | 2022年 / 27卷 / 18期
关键词
isatin; indole; imidazo[2; 1-b]thiazole; antimicrobial agents; cytotoxicity; ANTIPROLIFERATIVE EVALUATION; EFFICIENT SYNTHESIS; DESIGN; ANTIBACTERIAL; DERIVATIVES; ANTIFUNGAL; ANALOGS; BEARING;
D O I
10.3390/molecules27185781
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
Isatin and its derivatives are important heterocycles found in nature and present in numerous bioactive compounds which possess various biological activities. Moreover, it is an essential building block in organic synthesis. The discovery of novel compounds active against human pathogenic bacteria and fungi is an urgent need, and the isatin may represent the suitable scaffold in the design of biologically relevant antimicrobials. A small library of 18 isatin hybrids was synthetized and evaluated for their antimicrobial potential on three reference strains: S. aureus, E. coli, both important human pathogens infamous for causing community- and hospital-acquired severe systemic infections; and C. albicans, responsible for devastating invasive infections, mainly in immunocompromised individuals. The study highlighted two lead compounds, 6k and 6m, endowed with inhibitory activity against S. aureus at very low concentrations (39.12 and 24.83 mu g/mL, respectively).
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页数:12
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