46
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Synthesis, Structure, Electrochemistry, and Spectral Characterization of Bis-Isatin Thiocarbohydrazone Metal Complexes and Their Antitumor Activity Against Ehrlich Ascites Carcinoma in Swiss Albino Mice

      research-article
      1 , 1 , * , 2
      Metal-Based Drugs
      Hindawi Publishing Corporation

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The synthesis, structure, electrochemistry, and biological studies of Co(II), Ni(II), Cu(II), and Zn(II) complexes of thiocarbohydrazone ligand are described. The ligand is synthesized starting from thiocarbohydrazide and isatin. It is evident from the IR data that in all the complexes, only one part of the ligand is coordinated to the metal ion resulting mononuclear complexes. The ligand coordinates essentially through the carbonyl oxygen of the isatin fragment, the nitrogen atom of the azomethine group, and sulfur atom after deprotonation to give five membered rings. H 1 NMR spectrum of the ligand shows only one set of signals for the aromatic protons, while the NH of isatin and NH of hydrazone give rise to two different singlets in the 11–14 ppm range. The formulations, [Cu(L)Cl] · 2 H 2 O, [Cu(L)(C H 3 COO)] · 2 H 2 O, [Ni(L)Cl], [Ni(L)(C H 3 COO)], [Co( L 2 )], and [Zn( L 2 )] · 2 H 2 O are in accordance with elemental analyses, physical, and spectroscopic measurements. The complexes are soluble in organic solvents. Molar conductance values in DMF indicate the nonelectrolytic nature of the complexes. Copper complex displays quasireversible cyclic voltametric responses with Ep near 0.659 v and 0.504 v Vs Ag/AgCl at the scan rate of 0.1 V/s. Copper(II) complexes show a single line EPR signals. For the observed magnetic moment and electronic spectral data possible explanation has been discussed. From all the available data, the probable structures for the complexes have been proposed. The compounds synthesized in present study have shown promising cytotoxic activity when screened using the in vitro method and at the same time were shown to have good activity when tested using the Ehrlich ascites carcinoma (EAC) model. The antimicrobial screening showed that the cobalt complex possesses enhanced antimicrobial activity towards fungi.

          Related collections

          Most cited references58

          • Record: found
          • Abstract: not found
          • Article: not found

          The use of conductivity measurements in organic solvents for the characterisation of coordination compounds

          W.J. Geary (1971)
            Bookmark
            • Record: found
            • Abstract: not found
            • Book: not found

            Inorganic Electronic Spectroscopy,

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Distortion of fungal hyphae in the presence of certain inhibitors.

                Bookmark

                Author and article information

                Journal
                Met Based Drugs
                MBD
                Metal-Based Drugs
                Hindawi Publishing Corporation
                0793-0291
                1687-5486
                2008
                19 November 2007
                : 2008
                : 362105
                Affiliations
                1P. G. Department of Studies in Chemistry, Karnatak University, Dharwad 580 003, India
                2Department of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal 576 104, India
                Author notes

                Recommended by Jannie C. Swarts

                Article
                10.1155/2008/362105
                2259242
                18320020
                81975731-6e68-4895-93c7-10c3acd16083
                Copyright © 2008 M. P. Sathisha et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 May 2007
                : 7 July 2007
                : 6 August 2007
                Categories
                Research Article

                Pharmacology & Pharmaceutical medicine
                Pharmacology & Pharmaceutical medicine

                Comments

                Comment on this article