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, 209-214]. Our previous study on AR-1 and its linearderivative showed that disulfide bridge and the amphipat hic â-sheet structure of the AR-1 play important rolesin their biological activities. AR-1 ha s high antibacterial activity but it also displays hemolytic activity againsthuman red blood cells. In order to develop more potent and more bacterial cell selective peptide, we designedand synthesized a new derivative, AR-1-C (RW

Cell Selectivity of Arenicin-1 and Its Derivative with Two Disulfide Bonds