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Antibacterial and Antifungal Activity of Zinc(II) Carboxylates With/Without N-Donor Organic Ligands

The antibacterial and antifungal activity of zinc(II) carboxylates with composition Zn(RCOO)(2)•nH(2)O(R =H-, CH(3)(-), CH(3)CH(2)CH(2)(-), (CH(3))(2)CH-, XCH(2)(-), X=Cl, Br, I, n=0 or 2), [ZnX(2)(Nia(+)CH(2)COO(-))(2)](Nia=nicotinamide, X=Cl, Br, I) and [Zn(XCH(2)COO)(2)(Caf)(2)]•2H(2)O (Car=caffe...

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Detalles Bibliográficos
Autores principales: Zelenák, V., Györyová, K., Mlynarcík, D.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365280/
https://www.ncbi.nlm.nih.gov/pubmed/18476005
http://dx.doi.org/10.1155/MBD.2002.269
Descripción
Sumario:The antibacterial and antifungal activity of zinc(II) carboxylates with composition Zn(RCOO)(2)•nH(2)O(R =H-, CH(3)(-), CH(3)CH(2)CH(2)(-), (CH(3))(2)CH-, XCH(2)(-), X=Cl, Br, I, n=0 or 2), [ZnX(2)(Nia(+)CH(2)COO(-))(2)](Nia=nicotinamide, X=Cl, Br, I) and [Zn(XCH(2)COO)(2)(Caf)(2)]•2H(2)O (Car=caffeine, X=Cl, Br) is studied against bacterial strains Staphylococcus aureus, Escherichia coli and yeast Candida albicans. The structural types are assigned to the prepared compounds and the influence of (i) carboxylate chain length, (ii) substitution of hydrogen atom of carboxylate by halogen and (iii) presence of N-donor organic ligands on the biological activity is discussed.