Copyright (c) 2024 Dr.G.PUTHILIBAI GURUSAMY, M. Suganya Puthili
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis, Spectral Characterization, Antibacterial and Anticancer Evaluation of Novel Isoniazid based Schiff Base Ligand derived Transition Metal Complexes
Corresponding Author(s) : M. Suganya
Asian Journal of Chemistry,
Vol. 36 No. 3 (2024): Vol 36 Issue 3, 2024
Abstract
A novel isoniazid based Schiff base ligand was synthesized by the condensation of 5-acetyl-N-(adamantan-2-yl)thiophene-2-carboxamide (1 mmol) and isoniazid (1 mmol). Metal complexes were prepared by reacting the Schiff base with metal(II) chloride (M = Ni2+, Cu2+ and Co2+), formed the novel metal coordination compound. The synthesized ligand and metal complexes were characterized by 1H NMR, mass spectral, UV-visible, IR & EPR spectral studies, themogravimetric analysis, cyclic voltametry and were screened with both Gram-positive and Gram-negative bacterias to evaluate the antibacterial activity by disc diffusion method. The zone of inhibition of the antibacterial assay demonstrated that all the three metal(II) complexes are active against the four bacterias, showed increased activity with increase in concentration and is more active against S. aureas at all concentrations. The systhesized complexes were also evaluated for its anticancer activities, only Ni(II) and Co(II) complexes showed the moderate levels of cytotoxicity activity.
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- A. Bessette and G.S. Hanan, Chem. Soc. Rev., 43, 3342 (2014); https://doi.org/10.1039/C3CS60411J
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References
A. Bessette and G.S. Hanan, Chem. Soc. Rev., 43, 3342 (2014); https://doi.org/10.1039/C3CS60411J
E.V. Suslov, K. Yu Ponomarev, K.P. Volcho and N.F. Salakhutdinov, Russ. J. Bioorg. Chem., 47, 1133 (2021); https://doi.org/10.1134/S1068162021060236
J.M. Cameron, G. Guillemot, T. Galambos, S.S. Amin, E. Hampson, K.M. Haidaraly, G.N. Newton and G. Izzet, Chem. Soc. Rev., 51, 293 (2022); https://doi.org/10.1039/D1CS00832C
A. Ragab, M.S. Abusaif, D.S. AboulMagd, M.M.S. Wassel, G.A.M. Elhagali and Y.A. Ammar, Drug Dev. Res., 83, 1305 (2022); https://doi.org/10.1002/ddr.21960
G. Puthilibai, S. Vasudhevan, S.K. Rani and G. Rajagopal, Spectrochim. Acta A Mol. Biomol. Spectrosc., 72, 796 (2009); https://doi.org/10.1016/j.saa.2008.11.019
D.B. Shinde, R. Pawar, J. Vitore, D. Kulkarni, S. Musale and P.S. Giram, Polym. Adv. Technol., 32, 4204 (2021); https://doi.org/10.1002/pat.5457
R. Shah and P.K. Verma, Chem. Cent. J., 12, 137 (2018); https://doi.org/10.1186/s13065-018-0511-5
T. Boibessot, C.P. Zschiedrich, A. Lebeau, D. Bénimèlis, C. Dunyach-Remy, J.P. Lavigne, H. Szurmant, Z. Benfodda and P. Meffre, J. Med. Chem., 59, 8830 (2016); https://doi.org/10.1021/acs.jmedchem.6b00580
G. Puthilibai, V. Devatarika, B. Haewon, S.S. Behura, H.K. Lautre, V. Subha, P. Sangwan and J. Sunil, Bull. Chem. Soc. Ethiop., 37, 1133 (2023); https://doi.org/10.4314/bcse.v37i5.6
B. Englinger, C. Pirker, P. Heffeter, A. Terenzi, C.R. Kowol, B.K. Keppler and W. Berger, Chem. Rev., 119, 1519 (2018); https://doi.org/10.1021/acs.chemrev.8b00396
M.R. Slobodian, J.D. Petahtegoose, A.L. Wallis, D.C. Levesque and T.J. Merritt, Toxics, 9, 269 (2021); https://doi.org/10.3390/toxics9100269
G Puthilibai, S Vasudhevan, S John Mary, Mater. Today: Proc., 36, 809 (2021); https://doi.org/10.1016/j.matpr.2020.07.008
P. Ghanghas, A. Choudhary, D. Kumar and K. Poonia, Inorg. Chem. Commun., 130, 108710 (2021); https://doi.org/10.1016/j.inoche.2021.108710
G. Puthilibai, A. Lazha, T. Pushpa Malini, S. Chitra Devi, V. Devatarika and S. Vasudhevan, AIP Conf. Proc., 2464, 040003 (2022); https://doi.org/10.1063/5.0083319
O.Q. Munro, S.D. Strydom and C.D. Grimmer, New J. Chem., 28, 34 (2004); https://doi.org/10 .1039/B305946D
C. Fabbro, S. Armani, L.-E. Carloni, F. De Leo, J. Wouters and D. Bonifazi, Eur. J. Org. Chem., 2014, 5487 (2014); https://doi.org/10.1002/ejoc.201402654
M.A. Hadi and I.K. Kareem, Res. J. Adv. Sci., 1, 1 (2020); https://doi.org/10.6084/rjas.v1i1.251
G. Puthilibai, S. Vasudhevan and G. Rajagopal, Acta Crystallogr., E64, o1333 (2008); https://doi.org/10.1107/S1600536808017443
M.A. Manan and M.F. Mohammat, Trends in Sciences, 19, 23 (2022); https://doi.org/10.48048/tis.2022.1500
M. Pervaiz, S. Sadiq, A. Sadiq, U. Younas, A. Ashraf, Z. Saeed, M. Zuber and A. Adnan, Coord. Chem. Rev., 447, 214128 (2021); https://doi.org/10.1016/j.ccr.2021.214128
A. Afrin and P.C. Swamy, Coord. Chem. Rev., 494, 215327 (2023); https://doi.org/10.1016/j.ccr.2023.215327
M.S. Refat, M.Y. El-Sayed and A.M. Adam, J. Mol. Struct., 1038, 62 (2013); https://doi.org/10.1016/j.molstruc.2013.01.059
Y. Song, Z. Xu, Q. Sun, B. Su, Q. Gao, H. Liu and J. Zhao, J. Coord. Chem., 61, 1212 (2008); https://doi.org/10.1080/00958970701509768
A.A. Al-Riyahee, H.H. Hadadd and B.H. Jaaz, Orient. J. Chem., 34, 2927 (2018); https://doi.org/10.13005/OJC%2F340632
M. Kuate, M.A. Conde, E. Ngandung Mainsah, A.G. Paboudam, F.M. Tchieno, K.I. Ketchemen, I. Tonle Kenfack and P.T. Ndifon, J. Chem., 2020, 5238501 (2020); https://doi.org/10.1155/2020/5238501
V.P. Singh, Spectrochim. Acta A Mol. Biomol. Spectrosc., 71, 17 (2008); https://doi.org/10.1016/j.saa.2007.11.004
S. Chandra and Sangeetika, Spectrochim. Acta A Mol. Biomol. Spectrosc., 60, 147 (2004); https://doi.org/10.1016/S1386-1425(03)00220-8
K. Venkateswarlu, N. Ganji, S. Daravath, K. Kanneboina and K. Rangan, Polyhedron, 171, 86 (2019); https://doi.org/10.1016/j.poly.2019.06.048
J. Devi, S. Sharma, S. Kumar, B. Kumar, D. Kumar, D.K. Jindal and S. Das, Appl. Organomet. Chem., 36, 6760 (2022); https://doi.org/10.1002/aoc.6760