Biological Activity and Molecular Structures of Bis(benzimidazole) and Trithiocyanurate Complexes
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26053490
PubMed Central
PMC6272323
DOI
10.3390/molecules200610360
PII: molecules200610360
Knihovny.cz E-zdroje
- Klíčová slova
- benzimidazole, biological activity, coordination compounds, single crystal X-ray diffraction, trimercaptotriazine, trithiocyanuric acid,
- MeSH
- antiinfekční látky chemie farmakologie MeSH
- benzimidazoly chemie farmakologie MeSH
- inhibiční koncentrace 50 MeSH
- mikrobiální testy citlivosti MeSH
- molekulární modely MeSH
- molekulární struktura * MeSH
- triaziny chemie farmakologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antiinfekční látky MeSH
- benzimidazoly MeSH
- bis-benzimidazole MeSH Prohlížeč
- triaziny MeSH
- trithiocyanuric acid MeSH Prohlížeč
1-(1H-Benzimidazol-2-yl)-N-(1H-benzimidazol-2-ylmethyl)methanamine (abb) and 2-(1H-benzimidazol-2-ylmethylsulfanylmethyl)-1H-benzimidazole (tbb) have been prepared and characterized by elemental analysis. These bis(benzimidazoles) have been further used in combination with trithiocyanuric acid for the preparation of complexes. The crystal and molecular structures of two of them have been solved. Each nickel atom in the structure of trinuclear complex [Ni3(abb)3(H2O)3(μ-ttc)](ClO4)3·3H2O·EtOH (1), where ttcH3 = trithiocyanuric acid, is coordinated with three N atoms of abb, the N,S donor set of ttc anion and an oxygen of a water molecule. The crystal of [(tbbH2)(ttcH2)2(ttcH3)(H2O)] (2) is composed of a protonated bis(benzimidazole), two ttcH2 anions, ttcH3 and water. The structure is stabilized by a network of hydrogen bonds. These compounds were primarily synthesized for their potential antimicrobial activity and hence their possible use in the treatment of infections caused by bacteria or yeasts (fungi). The antimicrobial and antifungal activity of the prepared compounds have been evaluated on a wide spectrum of bacterial and yeast strains and clinical specimens isolated from patients with infectious wounds and the best antimicrobial properties were observed in strains after the use of ligand abb and complex 1, when at least 80% growth inhibition was achieved.
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