In vitro screening of pentamidine analogs against bacterial and fungal strains

Abstract A series of linear pentamidine analogs exhibiting low cytotoxicity, active against Pneumocystis carinii , were evaluated for in vitro activities against bacterial and fungal strains. The majority of the tested bis-amidines exhibited marked activities against Gram-positive strains. In view of the fact that the highest potency was found for 1,5-bis(4-amidinophenoxy)-3-thiapentane dihydrochloride 1j with the S atom in the middle of the aliphatic linker, four new pentamidines bearing S atoms were synthesized and also evaluated against MRSA strains. N , N ′-Dialkylated pentamidines with S atoms in the linker are the promising lead structures for antimicrobials development.