Antifungal activity of Co(II) and Cu(II) complexes containing 1,3-bis(benzotriazol-1-yl)-propan-2-ol on the growth, virulence traits of fluconazole-resistant Candida: Synthesis, DFT calculations and biological activity

Author:

Murcia-Galán Ricardo A.1,Durán Sandra M.2,Leal Sandra M.2,Roa Martha V.2,Vargas Jose D.2,Herrera Laura V.3,Muñoz-Castro Alvaro4,MacLeod-Carey Desmond5,Naranjo Tonny W.6,Hurtado John J.1

Affiliation:

1. Universidad de los Andes

2. Universidad de Santander

3. Universidad Santo Tomás

4. Universidad San Sebastián

5. Universidad Autónoma de Chile

6. Corporación para Investigaciones Biológicas

Abstract

Abstract Relevant virulence traits in Candida are associated with the dimorphic change and biofilm formation, which became an important target to reduce the antifungal resistance. In this work, Co(II) complexes containing a benzotriazole derivative ligand showed a promising capacity of reduce these virulence traits. These complexes exhibited higher antifungal activities than the free ligands against all the Candida albicans and non-albicans strains tested, where compounds 2 and 4 showed minimum inhibitory concentration values between 15.62 and 125 µg mL− 1. Moreover, four complexes (25) of Co(II) and Cu(II) with benzotriazole ligand were synthesized. These compounds were obtained as air-stable solids and characterized by melting point, thermogravimetric analysis, infrared, Raman and ultraviolet/visible spectroscopy. The analysis of the characterization data allowed to identify that all the complexes had 1:1 (M:L) stoichiometries. Additionally, Density Functional Theory calculations were carried out for 2 and 3 to propose a probable geometry of both compounds. The conformer Da of 2 was the most stable conformer according to the Energy Decomposition Analysis; while the conformers of 3 have a fluxional behavior in this analysis that didn’t allow to recognize the most probable conformer. These results provide an important platform for the design of new compounds with antifungal activities and capacity of attack other target of relevance to reduce the antimicrobial resistance.

Publisher

Research Square Platform LLC

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