Tetrahedral copper(II) and zinc(II) coordination compounds from 5-nitroimidazole derivatives, viz. 1-(2-chloroethyl)-2-methyl-5-nitroimidazole (cenz) and ornidazole 1-(3-chloro-2-hydroxypropyl)-2-methyl-5-nitroimidazole (onz), were synthesized and spectroscopically characterized. Their molecular structures were determined by X-ray diffraction studies. The complexes [Cu(onz)X], [Zn(onz)X], [Cu(cenz)X] and [Zn(cenz)X] (X = Cl, Br), are stable in solution and exhibit positive LogD values that are in the range for molecules capable of crossing the cell membrane via passive difussion. Their biological activity against Toxoplasma gondi was investigated, and IC and lethal dose (LD) values were determined. The ornidazole copper(II) compounds showed very good antiparasitic activity in its tachyzoite morphology. The interaction of the coordination compounds with DNA was examined by circular dichroism, fluorescence (using intercalating ethidium bromide and minor groove binding Hoechst 33258) and UV-Vis spectroscopy. The copper(II) compounds interact with the minor groove of the biomolecule, whereas weaker electrostatic interactions take place with the zinc(II) compounds. The spectroscopic data achieved for the two series of complexes (namely with copper(II) and zinc(II) as metal center) agree with the respective DNA-damage features observed by gel electrophoresis.
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http://dx.doi.org/10.1007/s00775-023-02029-7 | DOI Listing |
ACS Omega
December 2024
Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam 781 039, India.
In a quest to explore interconvertible assemblies of hydrates of cobalt(II), copper(II), and zinc(II) 2,6-pyridinedicarboxylate (), complexes having cation of a chloro-substituted analogue N-{(10-chloroanthracen-9-yl)methyl}-3-(1H-imidazol-1-yl)propan-1-amine were investigated. In the case of cobalt and copper complexes, a crystallized stable hydrate and a less stable methanol hydrate were guided by concentration-dependent crystallizations. The unit-cells of the crystals of the methanol hydrates of the two cobalt and copper complexes each belong to the P1̅ space group but have different stoichiometries as well as large differences in packing.
View Article and Find Full Text PDFJ Inorg Biochem
November 2024
Department of Inorganic Chemistry, Faculty of Science, Palacký University, 17. listopadu 12, CZ-779 00 Olomouc, Czech Republic. Electronic address:
The copper(II), cobalt(II), and zinc(II) complexes with 2-(1H-benzimidazol-2-ylmethylsulfanylmethyl)-1H-benzimidazole (tbb) and 2-[2-[2-(1H-benzimidazol-2-yl)ethylsulfanyl]ethyl]-1H-benzimidazole (tebb), [Cu(tbb)Cl] (1), [Co(tbb)Cl] (2), [Zn(tbb)Cl] (3), [Cu(tebb)Cl(HO)]Cl (4), [Co(tebb)Cl]·nCHOH (5) and [Zn(tebb)Cl(HO)]Cl (6), have been prepared and evaluated for antiproliferative activity. The structure of (4) was proved by X-ray diffraction crystallography. The coordination compounds were tested for their cytotoxic activities in cancer cell lines in vitro.
View Article and Find Full Text PDFJ Inorg Biochem
February 2025
Faculty of Chemistry, University of Wroclaw, F. Joliot-Curie 14, 50-383 Wroclaw, Poland; Chemistry and Biochemistry, Florida International University, 11200 SW 8th St, Miami, FL 33199, United States. Electronic address:
Metal ion coordination is crucial in bacterial metabolism, while divalent metal ions serve as essential cofactors for various enzymes involved in cellular processes. Therefore, bacteria have developed sophisticated regulatory mechanisms to maintain metal homeostasis. These involve protein interactions for metal ion uptake, efflux, intracellular transport, and storage.
View Article and Find Full Text PDFACS Catal
November 2024
Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
The air-stable copper(II) catalyst [Cu(FOX-L1)(MeCN)][OTf] () is prepared from a fused meso-dipyridylbisoxazolidine (FOX-L1) and CuBr, followed by treatment with AgOTf. The compound is a catalyst for the dehydration of 1-phenylethanol to styrene (+HO) in over 95% yield at 1 mol % catalyst loading. Other alcohols (benzylic, tertiary, or allylic) are also efficiently dehydrated by this catalyst.
View Article and Find Full Text PDFSci Rep
October 2024
Department of Chemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.
This study introduces a novel ion-imprinted polymer for the ultrasensitive detection of mercury(II) in water. The ion-imprinted polymer was synthesized via a simple bulk polymerization process using methacrylic acid as the functional monomer, ethylene glycol dimethacrylate as the cross-linker, morpholine-4-carbodithioic acid phenyl ester as the chelating agent, and ammonium persulfate as the initiator. The electrochemical mercury(II) sensing capability of the ion-imprinted polymer was studied via the modification of a cost-effective carbon paste electrode.
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