References
- 1. Ł. Popiołek, Hydrazide-hydrazones as potential antimicrobial agents: overview of the literature since 2010, Med. Chem. Res. 26 (2017) 287–301; DOI 10.1007/s00044-016-1756-y
- 2. M. K. Dahlgren, C. E. Zetterström, Å. Gylfe, A. Linusson and M. Elofsson, Statistical molecular design of a focused salicylidene acylhydrazide library and multivariate QSAR of inhibition of type III secretion in the Gram-negative bacterium Yersinia, Bioorg. Med. Chem. 18 (2010) 2686–2703; https://doi.org/10.1016/j.bmc.2010.02.022
- 3. P. V. Bernhardt, P. Chin, P. C. Sharpe and D. R. Richardson, Hydrazone chelators for the treatment of iron overload disorders: iron coordination chemistry and biological activity, Dalton Trans. 30 (2007) 3232–3244; https://doi.org/10.1039/b704102k
- 4. K. Hruskova, P. Kovarikova, P. Bendova, P. Haskova, E. Mackova, J. Stariat, A. Vavrova, K. Vavrova and T. Simunek, Synthesis and initial in vitro evaluations of novel antioxidant aroylhydrazone iron chelators with increased stability against plasma hydrolysis, Chem. Res. Toxicol. 24 (2011) 290–302; https://doi.org/10.1021/tx100359t
- 5. P. Kovaríkova, Z. Mrkvičkova and J. Klimeš, Investigation of the stability of aromatic hydrazones in plasma and related biological material, J. Pharm. Biomed. Anal. 47 (2008) 360–370; https://doi.org/10.1016/j.jpba.2008.01.011
- 6. N. Galić, A. Dijanošić, D. Kontrec and S. Miljanić, Structural investigation of aroylhydrazones in dimethylsulphoxide/water mixtures, Spectrochim. Acta A95 (2012) 347–353; https://doi.org/10.1016/j.saa.2012.03.086
- 7. C. F. Da Costa, A. C. Pinheiro, M. V. De Almeida, M. C. Lourenço and M. V. De Souza, Synthesis and antitubercular activity of novel amino acid derivatives, Chem. Biol. Drug Des. 79 (2012) 216–222; https://doi.org/10.1111/j.1747-0285.2011.01269.x
- 8. M. C. Mandewale, B. Thorat, Y. Nivid, R. Jadhav, A. Nagarsekar and R. Yamgar, Synthesis, structural studies and antituberculosis evaluation of new hydrazone derivatives of quinoline and their Zn(II) complexes, J. Saudi Chem. Soc. 22 (2018) 218–228; https://doi.org/10.1016/j.jscs.2016.04.003
- 9. Y. Ozkay, Y. Tunali, H. Karaca and I. Işikdağ, Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazone moiety, Eur. J. Med. Chem. 45 (2010) 3293–3298; https://doi.org/10.1016/j.ejmech.2010.04.012
- 10. T. Benković, A. Kenđel, J. Parlov-Vuković, D. Kontrec, V. Chiş, S. Miljanić and N. Galić, Multiple dynamics of aroylhydrazone induced by mutual effect of solvent and light - spectroscopic and computational study, J. Mol. Liq. 255 (2018) 18–25; https://doi.org/10.1016/j.saa.2017.09.038
- 11. T. Benković, D. Kontrec, V. Tomišić, A. Budimir and N. Galić, Acid-base properties and kinetics of hydrolysis of aroylhydrazones derived from nicotinic acid hydrazide, J. Solution Chem. 45 (2016) 1227–1245; https://doi.org/10.1007/s10953-016-0504-8
- 12. European Committee for Antimicrobial Susceptibility Testing (EUCAST) of the European Society for Clinical Microbiology and Infectious Diseases (ESCMID), EUCAST Discussion Document E. Dis 5.1, Determination of minimum inhibitory concentrations (MICs) of antibacterial agents by broth dilution, Clin. Microbiol. Infect. 9 (2003) 1–7; https://doi.org/10.1046/j.1469-0691.2003.00790.x
- 13. M. C. Arendrup, J. Meletiadis, J. W. Mouton, K. Lagrou, Petr Hamal, J. Guinea, and the Subcommittee on Antifungal Susceptibility Testing (AFST) of the ESCMID European Committee for Antimicrobial Susceptibility Testing, EUCAST Definitive Document E. Def. 7.3.1. January 2017 - Method for the Determination of Broth Dilution Minimum Inhibitory Concentrations of Antifungal Agents for Yeasts; http://www.eucast.org/ast_of_fungi/methodsinantifungalsusceptibilitytesting/susceptibility_testing_of_yeasts/; last access date December 13, 2018.
- 14. J. Vlainić, I. Kosalec, K. Pavić, D. Hadjipavlou-Litina, E. Pontiki and B. Zorc, Insights into biological activity of ureidoamides with primaquine and amino acid moieties, J. Enzyme Inhib. Med. Chem. 33 (2018) 376–382; https://doi.org/10.1080/14756366.2017.1423067
- 15. S. Purser, P. R. Moore, S. Swallow and V. Gouverneur, Fluorine in medicinal chemistry, Chem. Soc. Rev. 37 (2008) 320–330;