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      Synthesis, Characterization, Antimicrobial and Antiproliferative Activity Evaluation of Cu(II), Co(II), Zn(II), Ni(II) and Pt(II) Complexes with Isoniazid-Derived Compound

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          Abstract

          Hydrazone complexes of Cu(II), Co(II), Zn(II), Ni(II) and Pt(II) with N-isonicotinoyl- N′-(3-metoxy-2 hydroxybenzaldehyde)-hydrazone ( HL) were synthesized and characterized by different physico-chemical techniques including elemental and thermal analysis, magnetic susceptibility measurements, molar electric conductivity, as well as IR (infrared), 1H-NMR and 13C-NMR (hydrogen and carbon nuclear magnetic resonance, UV-Vis (ultraviolet-visible), FAB (fast atom bombardment), EPR (electron paramagnetic resonance), and mass spectroscopies. The crystal structure of ligand was determined by single crystal X-ray diffraction studies. Spectral data showed that hydrazone behaves as an ONO tridentate ligand through the azomethine nitrogen, phenolate and keto oxygen atoms. For the copper(II) complexes, metal–ligand bonding parameters were evaluated from the EPR spectra. These parameters indicate the presence of in-plane π bonding. In addition, the f values of complexes 14 indicate small distortion from planarity. The effect of these complexes on proliferation of human breast cancer (MCF-7 and SKBR-3), human melanoma (A375), lung adenocarcinoma cells (NCI-H1573) and their antibacterial activity against Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus and Candida albicans strains were studied and compared with those of free ligand. The ligand and complexes 13 showed significant antimicrobial activity against the Gram-positive bacteria Staphylococcus aureus and Candida albicans in comparison to the control drugs. The complexes 24 could be potential antitumor agents, leading to a significant improvement of the cytotoxic activity when compared with HL.

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            Brine shrimp: a convenient general bioassay for active plant constituents.

            A method, utilizing brine shrimp (Artemia salina Leach), is proposed as a simple bioassay for natural product research. The procedure determines LC (50) values in microg/ml of active compounds and extracts in the brine medium. Activities of a broad range of known active compounds are manifested as toxicity to the shrimp. Screening results with seed extracts of 41 species of Euphorbiaceae were compared with 9KB and 9PS cytotoxicities. The method is rapid, reliable, inexpensive, and convenient as an in-house general bioassay tool.
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              The electronic properties and stereochemistry of mono-nuclear complexes of the copper(II) ion

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                Author and article information

                Contributors
                Role: Academic Editor
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
                MDPI
                1420-3049
                19 April 2017
                April 2017
                : 22
                : 4
                : 650
                Affiliations
                [1 ]Inorganic Chemistry Department, Faculty of Pharmacy, University of Medicine and Pharmacy “Carol Davila”, 6 Traian Vuia Street, 020956 Bucharest, Romania
                [2 ]Organic Chemistry Department, Faculty of Pharmacy, University of Medicine and Pharmacy “Carol Davila”, 6 Traian Vuia Street, 020956 Bucharest, Romania
                [3 ]Institute of Macromolecular Chemistry “Petru Poni”, 41A Grigore Ghica Voda Alley, 700487 Iasi, Romania; shova@ 123456icmpp.ro
                [4 ]Environmental and Food Chemistry Department, Faculty of Pharmacy, University of Medicine and Pharmacy “Victor Babeş”, 2nd Eftimie Murgu Sq., 300041 Timişoara, Romania; camelia.sass5@ 123456gmail.com
                [5 ]“Pius Brinzeu” Timișoara County Emergency Clinical Hospital, Oncogen Institute, 156 Liviu Rebreanu, 300723 Timişoara, Romania; genostem@ 123456yahoo.com
                [6 ]Functional Sciences Department, Faculty of Medicine, University of Medicine and Pharmacy “Victor Babeş”, 2 Eftimie Murgu Square, 300041 Timişoara, Romania
                [7 ]Pharmaceutical Botany and Cell Biology Department, Faculty of Pharmacy, University of Medicine and Pharmacy “Carol Davila”, 6 Traian Vuia Street, 020956 Bucharest, Romania; octav_olaru2002@ 123456yahoo.com
                [8 ]Pharmaceutical Biotechnology Department, Faculty of Pharmacy, University of Medicine and Pharmacy “Carol Davila”, 6 Traian Vuia Street, 020956 Bucharest, Romania; flavian_stefan@ 123456yahoo.com
                [9 ]Coordination Chemistry Department, Moldova State University, 60 Mateevici Street, 2009 Chisinau, Moldova; dociu1946@ 123456yahoo.com
                [10 ]Inorganic Chemistry Department, Faculty of Chemistry, University of Bucharest, 23 Dumbrava Rosie Street, 020462 Bucharest, Romania; t_rosu0101@ 123456yahoo.com
                [11 ]Pharmaceutical Physics Department, Faculty of Pharmacy, University of and Pharmacy “Carol Davila”, 6 Traian Vuia Street, 020956 Bucharest, Romania; doinadraganescu@ 123456yahoo.com
                Author notes
                [* ]Correspondence: elenaandmihaela@ 123456yahoo.com (E.P.); ilies_diana@ 123456hotmail.com (D.-C.I.); Tel.: +40-072-247-6215 (E.P.)
                Article
                molecules-22-00650
                10.3390/molecules22040650
                6154339
                28422067
                a1b0ce89-456e-481a-9c1b-1a26b6506713
                © 2017 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 26 March 2017
                : 14 April 2017
                Categories
                Article

                copper(ii),cobalt(ii),zinc(ii),nickel(ii) and platinum(ii) complexes,antimicrobial activity,human breast skbr-3 and mcf-7,human melanoma a375,lung adenocarcinoma cell nci-h1573

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