Antimicrobial Activity and Urease Inhibition of Schiff Bases Derived from Isoniazid and Fluorinated Benzaldehydes and of Their Copper(II) Complexes

Molecules. 2016 Dec 17;21(12):1742. doi: 10.3390/molecules21121742.

Abstract

In order to evaluate the influence of substitution on biological properties of Schiff bases and their metal complexes, a series of differently substituted fluorine-containing Schiff bases starting from the drug isoniazid (isonicotinylhydrazide) were prepared and their structures were established by single-crystal X-ray diffraction. Also, four copper(II) complexes of these Schiff bases were synthesized. The prepared compounds were evaluated for their antimicrobial activity and urease inhibition. Two of the Schiff bases exerted activity against C. albicans. All copper(II) complexes showed excellent inhibitory properties against jack bean urease, considerably better than that of the standard inhibitor acetohydroxamic acid.

Keywords: antimicrobial activity; copper(II) complexes; fluorine; isoniazid; urease inhibitors.

MeSH terms

  • Anti-Infective Agents / pharmacology
  • Benzaldehydes
  • Coordination Complexes / chemical synthesis
  • Coordination Complexes / chemistry*
  • Coordination Complexes / pharmacology
  • Copper
  • Crystallography, X-Ray
  • Escherichia coli
  • Halogenation
  • Inhibitory Concentration 50
  • Isoniazid
  • Molecular Structure
  • Schiff Bases / chemistry*
  • Schiff Bases / pharmacology
  • Structure-Activity Relationship
  • Urease / antagonists & inhibitors
  • X-Ray Diffraction

Substances

  • Anti-Infective Agents
  • Benzaldehydes
  • Coordination Complexes
  • Schiff Bases
  • Copper
  • Urease
  • Isoniazid