Design, Synthesis and Multitarget Biological Evaluation of Perfluoroalkylated Benzoylthiourea Compounds: From Biofilm Disruption to DNA Cleavage

High Resolution Image Download MS PowerPoint Slide In the present study, a series of benzoylthiourea compounds bearing a perfluorinated group (−C 8 F 17 ), namely N -((4-(heptadecafluorooctyl)phenyl)carbamothioyl)benzamide (1) and N -((3-(heptadecafluorooctyl)phenyl)carbamothioyl)benzamide (2) along with their non-fluorinated analogue, N -(phenylcarbamothioyl)benzamide (3), were synthesized and characterized. Subsequently, various biological properties of the thiourea derivatives 1, 2, and 3 were evaluated, with a particular focus on elucidating the effect of the fluorinated group. The free radical scavenging activities of these compounds were evaluated with ascorbic acid and Trolox standards. Antioxidant activity peaked at 84.56% for 1 and 74.22% for 3. While 1 and 2 showed 97.70 and 96.50% inhibitory effects on α-amylase at 6.25 mg/L, 3 demonstrated 74.90% inhibitory effect at 100 mg/L. All compounds also displayed effective DNA nuclease activity. Additionally, antimicrobial and antibiofilm activities of benzoylthiourea compounds were also investigated. The most resistant microorganisms to the tested compounds were found to be Escherichia coli and Pseudomonas aeruginosa . In contrast, the most sensitive microorganisms were found to be Legionella pneumophila subsp. pneumophila and Enterococcus faecalis . The biofilm formation inhibition activities of benzoylthiourea compounds against S. aureus were 71.79, 69.80, and 63.53%, and against P . aeruginosa were 53.52, 63.33, and 70.00%, respectively, at the highest concentration. These findings provide a basis for proposing perfluorinated benzoylthiourea derivatives as potential potent, selective, and multitarget medicinal agents.