Synthesis, ADMET Properties, and In Vitro Antimicrobial and Antibiofilm Activity of 5-Nitro-2-thiophenecarbaldehyde N-((E)-(5-Nitrothienyl)methylidene)hydrazone (KTU-286) against <i>Staphylococcus aureus</i> with Defined Resistance Mechanisms

The emergence of drug-resistant <i>Staphylococcus aureus</i> is responsible for high morbidity and mortality worldwide. New therapeutic options are needed to fight the increasing antimicrobial resistance among <i>S. aureus</i> in the clinical setting. We, therefore, character...

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Main Authors: Povilas Kavaliauskas (Author), Birute Grybaite (Author), Vytautas Mickevicius (Author), Ruta Petraitiene (Author), Ramune Grigaleviciute (Author), Rita Planciuniene (Author), Philip Gialanella (Author), Alius Pockevicius (Author), Vidmantas Petraitis (Author)
Format: Book
Published: MDPI AG, 2020-09-01T00:00:00Z.
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Summary:The emergence of drug-resistant <i>Staphylococcus aureus</i> is responsible for high morbidity and mortality worldwide. New therapeutic options are needed to fight the increasing antimicrobial resistance among <i>S. aureus</i> in the clinical setting. We, therefore, characterized the in silico absorption, distribution, metabolism, elimination, and toxicity (ADMET) and in vitro antimicrobial activity of 5-nitro-2-thiophenecarbaldehyde N-((E)-(5-nitrothienyl)methylidene)hydrazone (KTU-286) against drug-resistant <i>S. aureus</i> strains with genetically defined resistance mechanisms. The antimicrobial activity of KTU-286 was determined by CLSI recommendations. The ADMET properties were estimated by using in silico modeling. The activity on biofilm integrity was examined by crystal violet assay. KTU-286 demonstrated low estimated toxicity and low skin permeability. The highest antimicrobial activity was observed among pan-susceptible (Pan-S) <i>S. aureus</i> (minimal inhibitory concentration (MIC) 0.5-2.0 µg/mL, IC<sub>50</sub> = 0.460 µg/mL), followed by vancomycin resistant <i>S. aureus</i> (VRSA) (MIC 4.0 µg/mL, IC<sub>50</sub> = 1.697 µg/mL) and methicillin-resistant <i>S. aureus</i> (MRSA) (MIC 1.0-16.0 µg/mL, IC<sub>50</sub> = 2.282 µg/mL). KTU-286 resulted in significant (<i>p</i> < 0.05) loss of <i>S. aureus</i> biofilm integrity in vitro. Further studies are needed for a better understanding of safety, synergistic relationship, and therapeutic potency of KTU-286.
Item Description:10.3390/antibiotics9090612
2079-6382