Design of antibacterial peptide-like conjugated molecule with broad spectrum antimicrobial ability
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摘要:
Increasing multidrug-resistant (MDR) superbugs emerge worldwide causing a public health crisis.Consequently,it is urgent to find new antibiotics with efficient broad-spectrum antimicrobial activity.By virtue of versatility in molecular design,a new peptide-like cell membrane-broken molecule,oligo-(7,7'-bifluoren-benzo[c][1,2,5]thiadiazole) (OFBT) possessing a conjugated backbone and eight pendant guanidyl moieties was designed and synthesized.OFBT exhibits favorable broad-spectrum of antimicrobial activity to pathogens including Gram-negative and Gram-positive bacteria,and fungi with the minimum inhibitory concentration (MIC) below 3.0 μM.Moreover,OFBT exhibits high selectivity for pathogens over human cells to make it a promising broad spectrum antimicrobial agent.