The in vitro antimycobacterial activity of cobalt(II) and copper(II) complexes of some fluorinated isonicotinoylhydrazones was evaluated in a TB-infected macrophage model; all metalcomplexes exhibited excellent activity against Mycobacterium tuberculosis Erdman growing within macrophages, at concentrations much lower than in culture media. Moreover complexes 1b and 2a displayed EC(99) values lower than that of the parent-drug, isoniazid. In addition, all tested metalchelates significantly inhibited the growth of single-drug-resistant M. tuberculosis strains; complexes 1a and 2a also possessed moderate activity against Mycobacterium avium complex.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.bmcl.2004.09.052 | 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
March 2025
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 PDFInorg Chem
November 2024
Department of Chemistry, University at Buffalo, The State University of New York, Buffalo, New York14260, United States.
Macromolecules
October 2024
Material Research and Technology Department, Luxembourg Institute of Science and Technology, 28 Avenue des Hauts-Fourneaux, 4362 Esch-sur-Alzette, Luxembourg.
Oxidative chemical vapor deposition (oCVD) stands as an attractive approach for the synthesis, engineering, and integration of conjugated polymers for advanced electronic and optoelectronic applications. In oCVD, the oxidant significantly influences the conformational and optoelectronic properties of the resulting conjugated polymer thin films. In this work, triflate salts of iron(III) and copper(II) (Fe(OTf) and Cu(OTf), respectively) are investigated for the first time as suitable alternative oxidants to the widely used iron(III) chloride (FeCl) for the oCVD of conjugated polymers.
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.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!