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Synthesis,spectral characterization,theoretical, antimicrobial,DNA interaction and in vitro anticancer studies of Cu(II) and Zn(II) complexes with pyrimidine-morpholine based Schiff base ligand
Authors:M. Sankarganesh  J. Rajesh  G.G. Vinoth Kumar  M. Vadivel  L. Mitu  R. Senthil Kumar  J. Dhaveethu Raja
Affiliation:1. Chemistry Research Centre, Mohamed Sathak Engineering College, Kilakarai-623 806, Ramanathapuram (Dist), Tamil Nadu, India;2. Department of Nature Sciences, University of Pitesti, Pitesti 110040, Romania;3. Department of Pharmaceutical Chemistry, Swami Vivekanandha College of Pharmacy, Elayampalyam, Trichengode-637 005, Namakkal (Dist), Tamilnadu, India
Abstract:Novel Cu(II) (1) and Zn(II) (2) complexes with 4-(1-(4-morpholinophenyl)ethylideneamino)pyrimidine-5-carbonitrile) (L) have been synthesized and characterized by various spectroscopic and analytical techniques. DFT (density functional theory) studies result confirms that, LMCT mechanism have been done between L and M(II) ions. The antimicrobial studies indicate that the ligand L and complexes 1 & 2 exhibit higher activity against the E. coli bacteria and C. albicans fungi. The groove binding mode of ligand L and complexes 1 & 2 with CT-DNA have been confirmed by electronic absorption, competitive binding, viscometric and cyclic voltammetric studies. The electronic absorption titration of ligand L and complexes 1 & 2 with DNA have been carried out in different buffer solutions (pH 4.0, 7.0 & 10.0). The Kb values of ligand L and complexes 1 & 2 are higher in acidic buffer at pH 4.0 (Kb = 2.42 × 105, L; 2.8 × 105, 1; 2.65 × 105, 2) and the results revealed that, the interaction of synthesized compounds with DNA were higher in the acidic medium than basic and neutral medium. Furthermore, CT-DNA cleavage studies of ligand L and complexes 1 & 2 have been studied. The in vitro anticancer activities results show that complexes 1 & 2 have moderate cytotoxicity against cancer cell lines and low toxicity on normal cell line than ligand L.
Keywords:Pyrimidine  Morpholine  DFT  Antimicrobial  DNA binding  Anticancer studies
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