Synthesis of 3,5-Bis(trifluoromethyl)phenyl-Substituted Pyrazole Derivatives as Potent Growth Inhibitors of Drug-Resistant Bacteria.
Ibrahim S AlkhaibariHansa Raj KcSubrata RoyMohd K Abu-GazlehDavid F GilmoreMohammad Abrar AlamPublished in: Molecules (Basel, Switzerland) (2021)
Enterococci and methicillin-resistant S. aureus (MRSA) are among the menacing bacterial pathogens. Novel antibiotics are urgently needed to tackle these antibiotic-resistant bacterial infections. This article reports the design, synthesis, and antimicrobial studies of 30 novel pyrazole derivatives. Most of the synthesized compounds are potent growth inhibitors of planktonic Gram-positive bacteria with minimum inhibitory concertation (MIC) values as low as 0.25 µg/mL. Further studies led to the discovery of several lead compounds, which are bactericidal and potent against MRSA persisters. Compounds 11, 28, and 29 are potent against S. aureus biofilms with minimum biofilm eradication concentration (MBEC) values as low as 1 µg/mL.
Keyphrases
- staphylococcus aureus
- drug resistant
- methicillin resistant staphylococcus aureus
- multidrug resistant
- gram negative
- molecular docking
- biofilm formation
- acinetobacter baumannii
- anti inflammatory
- candida albicans
- small molecule
- case control
- pseudomonas aeruginosa
- high throughput
- ionic liquid
- helicobacter pylori infection
- structure activity relationship
- helicobacter pylori