DFT vibrational assignments, in vitro antifungal activity, genotoxic and acute toxicity determinations of the [Zn(phen)2(cnge)(H2O)](NO3)2·H2O complex

• Molecular DFT calculations of two Zn-coordinated cyanoguanidine tautomers.
• FTIR and Raman assignments assisted by DFT, in agreement with experimental.
• Improvement of the antifungal activity of cyanoguanidine by complexation.
• Improvement of the post antifungal effect of the ligand phenanthroline.
• Safety evaluation: non-mutagenic and non-toxic compound.

Calculations based on density functional methods were carried out for the [Zn(phen)2(cnge)(H2O)](NO3)2·H2O complex taking into account the presence of two different conformers for the cyanoguanidine ligand. The calculated geometrical parameters and the vibrational IR and Raman spectra were in agreement with the experimental data. On the other hand, the activities of the complex, the ligands and the metal against fungal strains have been measured. The complexation increased the antifungal activity of the metal and the ligand cyanoguanidine, and slightly decreased the antifungal activity of the ligand 1,10-phenanthroline against Candida albicans, C. albicans ATCC 10231 and Candida krusei (not against the others strains of Candida). The ligand 1,10-phenanthroline and the zinc complex showed in some cases higher activity than the common antifungal drug fluconazole. The complexation also increased the post-antifungal effect in the tested strains, except for Candida parapsilosis, even with a better efficiency than those of some conventional antifungal agents. Antifungal studies were coupled with safety evaluations using the Artemia salina and the Ames tests. The zinc complex behaved as a non-mutagenic and non-toxic compound at the tested concentrations. Moreover, the zinc complex could be safer than the ligand when used as an antifungal agent. Therefore, the interaction of zinc(II) with N-containing ligands may provide a promising strategy for the development of novel and more secure drugs with antifungal activity.

FTIR and Raman assignments have been assisted by DFT calculations of the vibrational behavior of the two Zn-coordinated cyanoguanidine tautomers. The complex showed higher antifungal activity than the common antifungal drug fluconazole behaving as a non-mutagenic and non-toxic compound at the tested concentrations.Figure optionsDownload as PowerPoint slide