The introduction of fluorine atoms or trifluoromethyl groups in short cationic peptides enhances their antimicrobial activity

The effect of introducing fluorine atoms or trifluoromethyl groups in either the peptidic chain or the C-terminal end of cationic pentapeptides is reported. Three series of amide and ester peptides were synthesised and their antimicrobial properties evaluated. An enhanced activity was found in those derivatives whose structure contained fluorine, suggesting an increase in their hydrophobicity.

The effect of introducing fluorine atoms or trifluoromethyl groups in cationic pentapeptides is reported. An enhanced antimicrobial activity was found suggesting an increase in their hydrophobicity.Figure optionsDownload as PowerPoint slide