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Synthesis, Characterization and in vitro Cytotoxicity Studies of Pentadentate Ligand and its Copper(II) Complexes
Corresponding Author(s) : Kannappan Geetha
Asian Journal of Chemistry,
Vol. 30 No. 2 (2018): Vol 30 Issue 2
Abstract
A pentadentate ligand was synthesized by reaction of 4-t-butyl-2,6-bis(chloromethyl)phenol and isonicotinic hydrazide. The ligand was characterized by UV-visible, FT-IR, 1H NMR, 13C NMR and mass spectrascopic techniques. The above ligand was coordinated with various copper precursors to form corresponding copper(II) complexes. The complexes were characterized by UV-visible, FT-IR, molar conductivity and cyclic voltammetry. The in vitro cytotoxicity of the ligand and its copper complexes were studied against Ehrlich ascites carcinoma (EAC) cells.
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References
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A. Decker and E.I. Solomon, Curr. Opin. Chem. Biol., 9, 152 (2005); https://doi.org/10.1016/j.cbpa.2005.02.012.
E.A. Lewis and W.B. Tolman, Chem. Rev., 104, 1047 (2004); https://doi.org/10.1021/cr020633r.
C.J. Grimes, D. Piszkiewicz and E.B. Fleischer, Proc. Natl. Acad. Sci. USA, 71, 1408 (1974); https://doi.org/10.1073/pnas.71.4.1408.
C. Culotta, M. Yang and T.V. O’Halloran, Biochim. Biophys. Acta, 1763, 747 (2006); https://doi.org/10.1016/j.bbamcr.2006.05.003.
C. Marzano, M. Pellei, F. Tisato and C. Santini, Anticancer. Agents Med. Chem., 9, 185 (2009); https://doi.org/10.2174/187152009787313837.
R. Tabti, N. Tounsi, C. Gaiddon, E. Bentouhami and L. Désaubry, Med. Sci., 7, 875 (2017); https://doi.org/10.4172/2161-0444.1000445.
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G. Ambrosi, M. Formica, V. Fusi, L. Giorgi and M. Micheloni, Coord. Chem. Rev., 252, 1121 (2008); https://doi.org/10.1016/j.ccr.2007.09.027.
R.J. Nahi and K.M. Hello, Al-Qadisiya J. Vet. Med. Sci., 7, 1 (2008)
M. Ashram, J. Incl. Phenom. Macrocycl. Chem., 54, 253 (2006); https://doi.org/10.1007/s10847-005-8648-y.
L.J. Daumann, K.E. Dalle, G. Schenk, R.P. McGeary, P.V. Bernhardt, D.L. Ollis and L.R. Gahan, Dalton Trans., 41, 1695 (2012); https://doi.org/10.1039/C1DT11187F.
J. Medvecká, J. Halaska, K. Jomova and J. Moncol, Acta Chim. Slovaca, 5, 15 (2012); https://doi.org/10.2478/v10188-012-0003-5.
S.J. Jenniefer and P.T. Muthiah, Chem. Cent. J., 7, 35 (2013); https://doi.org/10.1186/1752-153X-7-35.
M. Iqbal, S. Ali, N. Muhammad and M. Sohail,Polyhedron, 57, 83 (2013); https://doi.org/10.1016/j.poly.2013.04.020.
M. Iqbal, I. Ahmad, S. Ali, N. Muhammad, S. Ahmed and M. Sohail, Polyhedron, 50, 524 (2013); https://doi.org/10.1016/j.poly.2012.11.037.
G. Negrón-Silva, R. González-Olvera, D. Angeles-Beltrán, N. Maldonado-Carmona, A. Espinoza-Vázquez, M. Palomar-Pardavé, M. Romero-Romo and R. Santillan, Molecules, 18, 4613 (2013); https://doi.org/10.3390/molecules18044613.
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D. Menon K, S. Dharmapal, C.R. Achuthan and T.D. Babu, J. Pharmacogn. Phytochem., 3, 1 (2014).
P.V. Mahadimane and V. Vasudev, Int. J. Life Sci. Pharma Res., 3, L22 (2013).
M. Ozaslan, I.D. Karagoz, I.H. Kilic and M.E. Guldur, Afr. J. Biotechnol., 10, 2375 (2011).
A.F. Abd El-Aziz, M.E. Hefni and A.M. Shalaby, Int. J.Curr. Res. Acad. Rev., 2, 330 (2014).
L. Giri and V.R. Pedireddi, J. Mol. Struct., 1100, 455 (2015); https://doi.org/10.1016/j.molstruc.2015.07.064.
E. Pahontu, D.-C. Ilies, S. Shova, C. Paraschivescu, M. Badea,A. Gulea and T. Rosu, Molecules, 20, 5771 (2015); https://doi.org/10.3390/molecules20045771.
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