Antibacterial and antifungal properties of guanylhydrazones

Vladimir Ajdačić, Jelena Lazić, Marija Mojičević, Sandra Šegan, Jasmina Nikodinović-Runić, Igor Opsenica

Abstract


A series of novel guanylhydrazones were designed, synthesized and characterized. All the compounds were screened for their antibacterial and antifungal activity. Compounds 26 and 27 showed excellent antibacterial activities against Staphylococcus aureus ATCC 25923 and Micrococcus luteus ATCC 379 with minimal inhibitory concentrations of 4 µg/mL, and good antifungal activity against Candida parapsilosis ATCC 22019. These results suggested that selected guanylhydrazones could serve as promising leads for the improved antimicrobial development.


Keywords


guanylhydrazones; iminoguanidines; antibacterial activity; antifungal activity; Candida spp

References


M. Oliveira, I. Serrano, Frontiers in Antimicrobial Agents: The Challenging of Antibiotic Resistance in the Development of New Therapeutics, Bentham Science Publ., Sharjah, 2015

M. A. Pfaller, S. A. Messer, G. J. Moet, R. N. Jones, M. Castanheira, Int. J. Antimicrob. Agents 38 (2011) 65

a) P. Ulrich, A. Cerami, J. Med. Chem. 27 (1984) 35; b) M. N. Borges, J. C. Messeder, J. D. Figueroa-Villar, Eur. J. Med. Chem. 39 (2004) 925; c) Z. Li, M. Khaliq, Z. Zhou, C. B. Post, R. J. Kuhn, M. Cushman, J. Med. Chem. 51 (2008) 4660; d) A. S. Mayhoub, M. Khaliq, C. Botting, Z. Li, R. J. Kuhn, M. Cushman, Bioorg. Med. Chem. 19 (2011) 3845; e) H. Mohammad, A. S. Mayhoub, A. Ghafoor, M. Soofi, R. A. Alajlouni, M. Cushman, M. N. Seleem, J. Med. Chem. 57 (2014) 1609; f) H. Mohammad, P. V. N. Reddy, D. Mon¬teleone, A. S. Mayhoub, M. Cushman, M. N. Seleem, Eur. J. Med. Chem. 94 (2015) 306

V. Ajdačić, L. Senerovic, M. Vranić, M. Pekmezovic, V. Arsic-Arsnijevic, A. Veseli¬no-vic, J. Veselinovic, B. A. Šolaja, J. Nikodinovic-Runic, I. M. Opsenica, Bioorg. Med. Chem. 24 (2016) 1277

V. Ajdačić, S. Stepanović, M. Zlatović, M. Gruden, I. M. Opsenica, Synthesis 48 (2016) 4423

T. Hosoya, H. Aoyama,T. Ikemoto,Y. Kihara,T. Hiramatsu, M. Endo, M. Suzuki, Bioorg. Med. Chem. 11 (2003) 663

J. C. Bussolari, D. C. Rehborn, Org. Lett. 1 (1991) 965

K. L. Milkiewicz, D. J. Parks, T. Lu, Tetrahedron Lett. 44 (2013) 4257




DOI: http://dx.doi.org/10.2298/JSC170213033A

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