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1

Pharmaceutical Chemistry Department, University of Medicine and Pharmacy Carol Davila, Bucharest, Romania

2

Microbiology Department, Faculty of Biology, University of Bucharest, Ale. Portocalelor 1-4, Bucharest 60101, Romania

3

National Institute for Research and Development in Microbiology and Immunology -Cantacuzino-, Spl. Independentei 103, Bucharest 060031, Romania





*

Author to whom correspondence should be addressed.



Abstract A number of acylthioureas, 2-4-methylphenoxymethyl-N-aryl-carbamothioylbenzamides aryl = 3,5-dichlorophenyl, 2,3-dichlorophenyl, 3,4-dichloro-phenyl, 2,4,5-trichlorophenyl, 3,4,5-trichlorophenyl, 2-bromophenyl, 2,4-dibromophenyl, 2,5-dibromophenyl, 2-iodophenyl, 3-fluorophenyl, 2,3,4-trifluorophenyl, 2,4,5-trifluoro-phenyl, 2,4,6-trifluorophenyl have been synthesized, characterized by elemental analysis, IR and NMR spectroscopy and tested for their interaction with bacterial cells in free and adherent state. The anti-pathogenic activity was correlated with the presence of one iodine, bromide or fluorine, and two or three chloride atoms on the N-phenyl substituent of the thiourea moiety, being significant especially on Pseudomonas aeruginosa and Staphylococcus aureus strains, known for their ability to grow in biofilms. Our results demonstrate the potential of these derivatives for further development of novel anti-microbial agents with antibiofilm properties.

Keywords: acylthioureas; benzamides; 2-4-methylphenoxymethylbenzoic acid; antimicrobial activity; bacterial biofilm acylthioureas; benzamides; 2-4-methylphenoxymethylbenzoic acid; antimicrobial activity; bacterial biofilm





Autor: Carmen Limban 1, Luminita Marutescu 2 and Mariana Carmen Chifiriuc 2,3,*

Fuente: http://mdpi.com/



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