Synthesis, characterization, and antimicrobial activity of silver carbene complexes derived from 4,5,6,7-tetrachlorobenzimidazole against antibiotic resistant bacteriaElectronic supplementary information (ESI) available. CCDC 845904-845910. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2dt00055e
Silver N -heterocyclic carbene complexes have been shown to have great potential as antimicrobial agents, affecting a wide spectrum of both Gram-positive and Gram-negative bacteria. A new series of three silver carbene complexes (SCCs) based on 4,5,6,7-tetrachlorobenzimidazole has been synthesized,...
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Sprache: | eng |
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Zusammenfassung: | Silver
N
-heterocyclic carbene complexes have been shown to have great potential as antimicrobial agents, affecting a wide spectrum of both Gram-positive and Gram-negative bacteria. A new series of three silver carbene complexes (SCCs) based on 4,5,6,7-tetrachlorobenzimidazole has been synthesized, characterized, and tested against a panel of clinical strains of bacteria. The imidazolium salts and their precursors were characterized by elemental analysis, mass spectrometry,
1
H and
13
C NMR spectroscopy, and single crystal X-ray diffraction. The silver carbene complexes,
SCC32
,
SCC33
, and
SCC34
were characterized by elemental analysis,
1
H and
13
C NMR spectroscopy, and single crystal X-ray diffraction. These complexes proved highly efficacious with minimum inhibitory concentrations (MICs) ranging from 0.25 to 6 μg mL
−1
. Overall, the complexes were effective against highly resistant bacteria strains, such as methicillin-resistant
Staphylococcus aureus
(MRSA), weaponizable bacteria, such as
Yersinia pestis
, and pathogens found within the lungs of cystic fibrosis patients, such as
Pseudomonas aeruginosa, Alcaligenes xylosoxidans
, and
Burkholderia gladioli
.
SCC33
and
SCC34
also showed clinically relevant activity against a silver-resistant strain of
Escherichia coli
based on MIC testing.
Three silver carbene complexes were synthesized and tested against a panel of clinical strains of bacteria. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c2dt00055e |