This work is licensed under a Creative Commons Attribution 4.0 International License.
DNA Binding Potency and Antimicrobial Analysis of New Indole and Pyrazolone Based Transition Metal(II) Complexes
Corresponding Author(s) : Murugan Selvamariammal
Asian Journal of Chemistry,
Vol. 32 No. 8 (2020): Vol 32 Issue 8, 2020
Abstract
Some novel series of 5-chloro isatin and 4-aminoantipyrine based Schiff bases with transition metal(II) complexes of (Cu, Co, Ni and Zn) have been prepared and characterized by physical, analytical and spectral data. The synthesized ligand behaves as a neutral tridentate is confirmed by spectral techniques. During the complexation, the stoichiometry ratio 1:2 (metal:ligand) is followed and an octahedral arrangement is adopted by all the metal complexes. The calf-thymus DNA interacts with complexes via an intercalative mode is studied by electronic absorption titration. Moreover, all these synthesized metal(II) complexes were tested against a set of bacterial and fungal strains reveals that complexes exhibit better activity than free ligand.
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- B.G. Tweedy, Phytopathology, 25, 910 (1964).
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- N. Raman, T. Chandrasekar, G. Kumaravel and L. Mitu, Appl. Organomet. Chem., 32, e3922 (2017);https://doi.org/10.1002/aoc.3922
- Y. Anjaneyulu and R.P. Rao, Synth. React. Inorg. Org. Chem., 16, 257 (1986); https://doi.org/10.1080/00945718608057530
References
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R. McRae, P. Bagchi, S. Sumalekshmy and C.J. Fahrni, Chem. Rev., 109, 4780 (2009); https://doi.org/10.1021/cr900223a
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S. Biswal, U. Sahoo, S. Sethy, H.K.S. Kumar and M. Banerjee, Asian J. Pharm. Clin. Res., 5, 1 (2012).
F. Lebon, N. Boggetto, M. Ledecq, F. Durant, Z. Benatallah, S. Sicsic, R. Lapouyade, O. Kahn, A. Mouithys-Mickalad, G. Deby-Dupont and M. Reboud-Ravaux, Biochem. Pharmacol., 63, 1863 (2002); https://doi.org/10.1016/S0006-2952(02)00918-8
J.E. Weder, C.T. Dillon, T.W. Hambley, B.J. Kennedy, P.A. Lay, J.R. Biffin, H.L. Regtop and N.M. Davies, Coord. Chem. Rev., 232, 95 (2002); https://doi.org/10.1016/S0010-8545(02)00086-3
F. Tisato, C. Marzano, M. Porchia, M. Pellei and C. Santini, Med. Res. Rev., 30, 708 (2010);https://doi.org/10.1002/med.20174
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G. Turan-Zitouni, M. Sivaci, F.S. Kiliç and K. Erol, Eur. J. Med. Chem., 36, 685 (2001); https://doi.org/10.1016/S0223-5234(01)01252-1
A.N. Lutsevich, K.I. Bender and O.V. Reshetko, Eksp. Klin. Farmakol., 58, 51 (1995).
S. Bondock, R. Rabie, H.A. Etman and A.A. Fadda, Eur. J. Med. Chem., 43, 2122 (2008); https://doi.org/10.1016/j.ejmech.2007.12.009
L. Kelland, Nat. Rev. Cancer, 7, 573 (2007); https://doi.org/10.1038/nrc2167
M.J. Hannon, Pure Appl. Chem., 79, 2243 (2007); https://doi.org/10.1351/pac200779122243
S.P. Fricker, Dalton Trans., 43, 4903 (2007); https://doi.org/10.1039/b705551j
Y. Xiong and L.N. Ji, Coord. Chem. Rev., 185-186, 711 (1999);https://doi.org/10.1016/S0010-8545(99)00019-3
V. Rajendiran, M. Murali, E. Suresh, S. Sinha, K. Somasundaram and M. Palaniandavar, Dalton Trans., 1, 148 (2008); https://doi.org/10.1039/B710578A
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P. Kalyani, M.M. Prakash, S. Kinthada and M. Adharvanachary, Int. J. Pharma Bio Sci., 3, 70 (2012).
G.S. Kurdekar, M.P. Sathisha, S. Budagumpi, N.V. Kulkarni, V.K. Revankar and D.K. Suresh, Med. Chem. Res., 21, 2273 (2012); https://doi.org/10.1007/s00044-011-9749-3
D. Poonam, R.Y. Amit, N.B. Jayshree and S.A. Anand, World Appl. Sci. J., 9, 1301 (2010).
T.M. Bhagat, D.K. Swamy and M.N. Deshpande, J. Chem. Pharm. Res., 4, 100 (2012).
R. Gomathi, A. Ramu and A. Murugan, Int. J. Innov. Res. Sci. Eng. Technol., 2, 5156 (2013).
R. Paulpandiyan, A. Arunadevi and N. Raman, Appl. Organomet. Chem., 31, e3792 (2017); https://doi.org/10.1002/aoc.3792
R. Rao, K.R. Reddy and K.N. Mahendra, Chem. Sci. Trans., 2, 1063 (2013);https://doi.org/10.7598/cst2013.527
E.C. Long and J.K. Barton, Acc. Chem. Res., 23, 271 (1990); https://doi.org/10.1021/ar00177a001
V.M. Manikandamathavan and B. Unni Nair, Eur. J. Med. Chem., 68, 244 (2013); https://doi.org/10.1016/j.ejmech.2013.07.051
S.K. Mal, M. Mitra, G. Kaur, V.M. Manikandamathavan, M.S. Kiran, A.R. Choudhury, B.U. Nair and R. Ghosh, RSC Adv., 4, 61337 (2014); https://doi.org/10.1039/C4RA09448D
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A. Wolfe, G.H. Shimer Jr. and T. Meehan, Biochemistry, 26, 6392 (1987); https://doi.org/10.1021/bi00394a013
Y.J. Liu, X.Y. Wei, W.J. Mei and L.X. He, Transition Met. Chem., 32, 762 (2007); https://doi.org/10.1007/s11243-007-0246-y
G.G. Mohamed, Spectrochim. Acta A Mol. Biomol. Spectrosc., 64, 188 (2006); https://doi.org/10.1016/j.saa.2005.05.044
M. Selvaganapathy and N. Raman, Inorg. Chem. Commun., 20, 238 (2012); https://doi.org/10.1016/j.inoche.2012.03.016
B.G. Tweedy, Phytopathology, 25, 910 (1964).
E.L. Chang, C. Simmers and D.A. Knight, Pharmaceuticals, 3, 1711 (2010); https://doi.org/10.3390/ph3061711
N. Raman, T. Chandrasekar, G. Kumaravel and L. Mitu, Appl. Organomet. Chem., 32, e3922 (2017);https://doi.org/10.1002/aoc.3922
Y. Anjaneyulu and R.P. Rao, Synth. React. Inorg. Org. Chem., 16, 257 (1986); https://doi.org/10.1080/00945718608057530