Synthesis, structures and urease inhibitory activity of cobalt(III) complexes with Schiff bases
[Display omitted] A series of new cobalt(III) complexes were prepared. They are [CoL1(py)3]·NO3 (1), [CoL2(bipy)(N3)]·CH3OH (2), [CoL3(HL3)(N3)]·NO3 (3), and [CoL4(MeOH)(N3)] (4), where L1, L2, L3 and L4 are the deprotonated form of N′-(2-hydroxy-5-methoxybenzylidene)-3-methylbenzohydrazide, N′-(2-h...
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Veröffentlicht in: | Bioorganic & medicinal chemistry 2016-01, Vol.24 (2), p.270-276 |
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Sprache: | eng |
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A series of new cobalt(III) complexes were prepared. They are [CoL1(py)3]·NO3 (1), [CoL2(bipy)(N3)]·CH3OH (2), [CoL3(HL3)(N3)]·NO3 (3), and [CoL4(MeOH)(N3)] (4), where L1, L2, L3 and L4 are the deprotonated form of N′-(2-hydroxy-5-methoxybenzylidene)-3-methylbenzohydrazide, N′-(2-hydroxybenzylidene)-3-hydroxylbenzohydrazide, 2-[(2-dimethylaminoethylimino)methyl]-4-methylphenol, and N,N′-bis(5-methylsalicylidene)-o-phenylenediamine, respectively, py is pyridine, and bipy is 2,2′-bipyridine. The complexes were characterized by infrared and UV–Vis spectra, and single crystal X-ray diffraction. The Co atoms in the complexes are in octahedral coordination. Complexes 1 and 4 show effective urease inhibitory activities, with IC50 values of 4.27 and 0.35μmolL−1, respectively. Complex 2 has medium activity against urease, with IC50 value of 68.7μmolL−1. While complex 3 has no activity against urease. Molecular docking study of the complexes with Helicobacter pylori urease was performed. |
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ISSN: | 0968-0896 1464-3391 |
DOI: | 10.1016/j.bmc.2015.12.013 |