Synthesis,structure, and biological evaluation of three Cu(II) and Ni(II) (E)-3-(3,4-dimethoxyphenyl)acrylate complexes with organic diamines as potential urease inhibitors |
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Abstract: | Three new complexes (1–3) have been synthesized and characterized by X-ray single crystal determination and evaluated for inhibitory activity on jack bean urease. All the complexes contained a new cinnamic acid derivative as the ligand (C11H12O4), (E)-3-(3,4-dimethoxyphenyl)acrylic acid, and crystallized in monoclinic C2/c space group. Complex 1 (C11H11O4)4(C3N2H8)2Cu2 (C3N2H8?=?1,2-diaminopropane) was obtained with a?=?20.488(2), b?=?19.596(2), c?=?15.2500(13), β?=?93.502(2)°, V?=?6111.2(10)?Å3, Z?=?4, R 1 ?=?0.0616, and wR 2 ?=?0.2059. Complex 2 (C11H11O4)4(C3N2H8)2Cu2 (C3N2H8=1,3-diaminopropane) was obtained with a?=?20.2494(12), b?=?19.5732(12), c?=?14.8940(8), β?=?96.884(2)°, V?=?5860.6(6)?Å3, Z?=?4, R 1 ?=?0.0409, and wR 2 ?=?0.1107. Complex 3 (C11H11O4)2(C2N2H6)2Ni2·H2O (C2N2H6?=?ethylenediamine) was obtained with a?=?28.359(2), b?=?6.5422(5), c?=?16.8587(14), β?=?101.359(2)°, V?=?3066.5(4)?Å3, Z?=?4, R 1 ?=?0.0422, and wR 2 ?=?0.1190. It was found that copper(II) complexes 1 IC50?=?4.71?μM] and 2 IC50?=?3.15?μM] showed strong inhibitory activity against jack bean urease compared with acetohydroxamic acid IC50?=?10.01?μM] as a positive reference. Unfortunately, 3 exhibited no inhibitory activity. |
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Keywords: | Cinnamic acid ligand Transition metal complexes Crystal structures Urease inhibitors |
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