Copyright (c) 2023 P. Yogalakshm, N. Banumathi
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis, Spectroscopic, Computational Structure Analysis, Molecular Docking, in vitro Antibacterial and in vivo Antipyretic Investigations of Transition Metal(II) Complexes
Corresponding Author(s) : P. Yogalakshmi
Asian Journal of Chemistry,
Vol. 35 No. 12 (2023): Vol 35 Issue 12, 2023
Abstract
Unsymmetrical Schiff base hydrazone complexes of cobalt(II), nickel(II) and zinc(II) were synthesized from oxalic dihydrazide, salicylaldehyde and ethyl acetoacetate. The ligand and its metal(II) complexes were characterized by elemental analysis, UV-visible, FT-IR, molar conductivity. To determine the biological activity, in vivo antipyretic as well as in vitro antibacterial activities were conducted along with molecular docking simulation, HOMO-LUMO and MEP calculations. The findings from the experimental and molecular docking investigations demonstrated that the ligand and all the metal(II) complexes has an ability to interact with E. coli 24kDa domain protein (PDB: 1KZN). Furthermore, these interactions were accompanied by favourable docking score values, indicating potential therapeutic implications. The quantum parameters and geometric optimization of the ligand and complexes were performed using DFT simulations.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- M.A. Malik, O.A. Dar, P. Gull, M.Y. Wani and A.A. Hashmi, Med. Chem. Commun., 9, 409 (2018); https://doi.org/10.1039/C7MD00526A
- A. Soroceanu andA. Bargan, Crystals, 12, 1436 (2022); https://doi.org/10.3390/cryst12101436
- M.S. More, P.G. Joshi, Y.K. Mishra and P.K. Khanna, Mater. Today Chem., 14, 100195 (2019); https://doi.org/10.1016/j.mtchem.2019.100195
- A. Kanwal, B. Parveen, R. Ashraf, N. Haider and K.G. Ali, J. Coord. Chem., 75, 2533 (2022); https://doi.org/10.1080/00958972.2022.2138364
- A.M. Abu-Dief and I.M.A. Mohamed, Beni-Suef Univ. J. Basic Appl. Sci., 4, 119 (2015); https://doi.org/10.1016/j.bjbas.2015.05.004
- R. Khojasteh and S.J. Matin, Russ. J. Appl. Chem., 88, 921 (2015); https://doi.org/10.1134/S107042721506004X
- S. Hou, J. Li, X. Huang, X. Wang, L. Ma, W. Shen, F. Kang and Z.-H. Huang, Appl. Sci., 7, 852 (2017); https://doi.org/10.3390/app7080852
- N. Goswami and D.M. Eichhorn, Inorg. Chim. Acta, 303, 271 (2000); https://doi.org/10.1016/S0020-1693(00)00047-5
- V.P. Singh, S. Singh and D.P. Singh J. Enzyme Inhib. Med. Chem., 27, 319 (2012); https://doi.org/10.3109/14756366.2011.588228
- V.P. Singh, A. Katiyar and S. Singh, Biometals, 21, 491 (2008); https://doi.org/10.1007/s10534-008-9136-9
- V.P. Singh and P. Gupta, J. Coord. Chem., 61, 3922 (2008); https://doi.org/10.1080/00958970802160974
- J.-L. Wang, Y.-Q. Zhao and B.-S. Yang, Inorg. Chim. Acta, 409, 484 (2014); https://doi.org/10.1016/j.ica.2013.09.001
- A.M. Hassan, A.H. Ahmed, H.A. Gumaa, B.H. Mohamed and A.M. Eraky, J. Chem. Pharm. Res., 7, 91 (2015).
- K.K. Narang and R.A. Lal, Curr. Sci., 46, 401 (1977).
- M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, G. A. Petersson, H. Nakatsuji, X. Li, M. Caricato, A. Marenich, J. Bloino, B. G. Janesko, R. Gomperts, B. Mennucci, H. P. Hratchian, J. V. Ortiz, A. F. Izmaylov, J. L. Sonnenberg, D. Williams-Young, F. Ding, F. Lipparini, F. Egidi, J. Goings, B. Peng, A. Petrone, T. Henderson, D. Ranasinghe, V. G. Zakrzewski, J. Gao, N. Rega, G. Zheng, W. Liang, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, K. Throssell, J. A. Montgomery, Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, T. Keith, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, J. M. Millam, M. Klene, C. Adamo, R. Cammi, J. W. Ochterski, R. L. Martin, K. Morokuma, O. Farkas, J. B. Foresman, and D. J. Fox, Gaussian, Inc., Wallingford CT, Gaussian 09, Revision A.02 (2016).
- Y. Yang, M.N. Weaver and K.M. Merz Jr., J. Phys. Chem. A, 113, 9843 (2009); https://doi.org/10.1021/jp807643p
- F.T.F. Tsai, O.M.P. Singh, T. Skarzynski, A.J. Wonacott, S. Weston, A. Tucker, R.A. Pauptit, A.L. Breeze, J.P. Poyser, R. O’Brien, J.E. Ladbury and D.B. Wigley, Proteins, 28, 41 (1997); https://doi.org/10.1002/(SICI)1097-0134(199705)28:1<41::AID-PROT4>3.0.CO;2-M
- O. Trott and A.J. Olson, J. Comput. Chem., 31, 455 (2010); https://doi.org/10.1002/jcc.21334
- R. Huey, G.M. Morris and S. Forli, Using AutoDock 4 and AutoDock Vina with AutoDockTools: A Tutorial. The Scripps Research Institute Molecular Graphics Laboratory (2012).
- D.S. Biovia, Discovery Studio Visualizer, San Diego, CA, USA, p. 936 (2017).
- Molinspiration Cheminformatics free web services; https://www.molinspiration.com (Accessed on 22 March 2023).
- M. Balouiri, M. Sadiki and S.K. Ibnsouda, J. Pharm. Anal., 6, 71 (2016); https://doi.org/10.1016/j.jpha.2015.11.005
- C.A. Winter, E.A. Risley and G.W. Nuss, Exp. Biol. Med., 111, 544 (1962); https://doi.org/10.3181/00379727-111-27849
- V.P. Singh, S. Singh, D.P Singh, K. Tiwari and M. Mishra, J. Mol. Struct., 1058, 71 (2014); https://doi.org/10.1016/j.molstruc.2013.10.046
- N. Sathya, G. Raja, N.P. Priya and C. Jayabalakrishnan, Appl. Organometal. Chem., 24, 366 (2010); https://doi.org/10.1002/aoc.1621
- V.P. Singh and P. Gupta, J. Coord. Chem., 61, 3922 (2008); https://doi.org/10.1080/00958970802160974
- B. Oritz and S.M. Park, Bull. Korean Chem. Soc., 21, 405 (2000); https://doi.org/10.5012/bkcs.2000.21.4.405
- M. Shakir, O.S.M. Nasman, A.K. Mohamed and S.P. Varkey, Polyhedron, 15, 1283 (1996); https://doi.org/10.1016/0277-5387(95)00379-7
- L.S. Chen and S.C. Cummings, Inorg. Chem., 17, 2358 (1978); https://doi.org/10.1021/ic50187a005
- R. Atkins, G. Brewer and E. Kokot, G.M. Mockler and E. Sinn, Inorg. Chem., 24, 127 (1985); https://doi.org/10.1021/ic00196a003
- M. Kwiatkowski, E. Kwiatkowski, A. Olechnowicz, D.M. Ho and E. Deutsch, J. Chem. Soc., Dalton Trans., 2497 (1990); https://doi.org/10.1039/DT9900002497
- A.B.P. Lever, Inorganic Electronic Spectroscopy, NewYork: Elsevier edn. 2 (1984).
- W.J. Geary, Coord. Chem. Rev., 7, 122 (1971); https://doi.org/10.1016/S0010-8545(00)80009-0
- V.P. Singh, S. Singh, D.P. Singh, K. Tiwari and M. Mishra, J. Mol. Struct., 1058, 71 (2014); https://doi.org/10.1016/j.molstruc.2013.10.046
- A. Amiri, M. Amirnasr, S. Meghdadi, K. Mereiter, V. Ghodsi and A. Gholami, Inorg. Chim. Acta, 362, 3934 (2009); https://doi.org/10.1016/j.ica.2009.05.020
- V.P. Singh, Spectrochim. Acta A Mol. Biomol. Spectrosc., 71, 17 (2008); https://doi.org/10.1016/j.saa.2007.11.004
- D.H. Pereira, F.A.L. Porta, R.T. Santiago, D.R. Garcia and T.C. Ramalho, Revista Virtual de Quimica, 8, 425 (2016); https://doi.org/10.5935/1984-6835.20160032
- D. Shin and Y. Jung, Phys. Chem. Chem. Phys., 24, 25740 (2022); https://doi.org/10.1039/D2CP03244A
- S. Murugavel, S. Deepa, C. Ravikumar, R. Ranganathan and P. Alagusundaram, J. Mol. Struct., 1222, 128961 (2020); https://doi.org/10.1016/j.molstruc.2020.128961
References
M.A. Malik, O.A. Dar, P. Gull, M.Y. Wani and A.A. Hashmi, Med. Chem. Commun., 9, 409 (2018); https://doi.org/10.1039/C7MD00526A
A. Soroceanu andA. Bargan, Crystals, 12, 1436 (2022); https://doi.org/10.3390/cryst12101436
M.S. More, P.G. Joshi, Y.K. Mishra and P.K. Khanna, Mater. Today Chem., 14, 100195 (2019); https://doi.org/10.1016/j.mtchem.2019.100195
A. Kanwal, B. Parveen, R. Ashraf, N. Haider and K.G. Ali, J. Coord. Chem., 75, 2533 (2022); https://doi.org/10.1080/00958972.2022.2138364
A.M. Abu-Dief and I.M.A. Mohamed, Beni-Suef Univ. J. Basic Appl. Sci., 4, 119 (2015); https://doi.org/10.1016/j.bjbas.2015.05.004
R. Khojasteh and S.J. Matin, Russ. J. Appl. Chem., 88, 921 (2015); https://doi.org/10.1134/S107042721506004X
S. Hou, J. Li, X. Huang, X. Wang, L. Ma, W. Shen, F. Kang and Z.-H. Huang, Appl. Sci., 7, 852 (2017); https://doi.org/10.3390/app7080852
N. Goswami and D.M. Eichhorn, Inorg. Chim. Acta, 303, 271 (2000); https://doi.org/10.1016/S0020-1693(00)00047-5
V.P. Singh, S. Singh and D.P. Singh J. Enzyme Inhib. Med. Chem., 27, 319 (2012); https://doi.org/10.3109/14756366.2011.588228
V.P. Singh, A. Katiyar and S. Singh, Biometals, 21, 491 (2008); https://doi.org/10.1007/s10534-008-9136-9
V.P. Singh and P. Gupta, J. Coord. Chem., 61, 3922 (2008); https://doi.org/10.1080/00958970802160974
J.-L. Wang, Y.-Q. Zhao and B.-S. Yang, Inorg. Chim. Acta, 409, 484 (2014); https://doi.org/10.1016/j.ica.2013.09.001
A.M. Hassan, A.H. Ahmed, H.A. Gumaa, B.H. Mohamed and A.M. Eraky, J. Chem. Pharm. Res., 7, 91 (2015).
K.K. Narang and R.A. Lal, Curr. Sci., 46, 401 (1977).
M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, G. A. Petersson, H. Nakatsuji, X. Li, M. Caricato, A. Marenich, J. Bloino, B. G. Janesko, R. Gomperts, B. Mennucci, H. P. Hratchian, J. V. Ortiz, A. F. Izmaylov, J. L. Sonnenberg, D. Williams-Young, F. Ding, F. Lipparini, F. Egidi, J. Goings, B. Peng, A. Petrone, T. Henderson, D. Ranasinghe, V. G. Zakrzewski, J. Gao, N. Rega, G. Zheng, W. Liang, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, K. Throssell, J. A. Montgomery, Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, T. Keith, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, J. M. Millam, M. Klene, C. Adamo, R. Cammi, J. W. Ochterski, R. L. Martin, K. Morokuma, O. Farkas, J. B. Foresman, and D. J. Fox, Gaussian, Inc., Wallingford CT, Gaussian 09, Revision A.02 (2016).
Y. Yang, M.N. Weaver and K.M. Merz Jr., J. Phys. Chem. A, 113, 9843 (2009); https://doi.org/10.1021/jp807643p
F.T.F. Tsai, O.M.P. Singh, T. Skarzynski, A.J. Wonacott, S. Weston, A. Tucker, R.A. Pauptit, A.L. Breeze, J.P. Poyser, R. O’Brien, J.E. Ladbury and D.B. Wigley, Proteins, 28, 41 (1997); https://doi.org/10.1002/(SICI)1097-0134(199705)28:1<41::AID-PROT4>3.0.CO;2-M
O. Trott and A.J. Olson, J. Comput. Chem., 31, 455 (2010); https://doi.org/10.1002/jcc.21334
R. Huey, G.M. Morris and S. Forli, Using AutoDock 4 and AutoDock Vina with AutoDockTools: A Tutorial. The Scripps Research Institute Molecular Graphics Laboratory (2012).
D.S. Biovia, Discovery Studio Visualizer, San Diego, CA, USA, p. 936 (2017).
Molinspiration Cheminformatics free web services; https://www.molinspiration.com (Accessed on 22 March 2023).
M. Balouiri, M. Sadiki and S.K. Ibnsouda, J. Pharm. Anal., 6, 71 (2016); https://doi.org/10.1016/j.jpha.2015.11.005
C.A. Winter, E.A. Risley and G.W. Nuss, Exp. Biol. Med., 111, 544 (1962); https://doi.org/10.3181/00379727-111-27849
V.P. Singh, S. Singh, D.P Singh, K. Tiwari and M. Mishra, J. Mol. Struct., 1058, 71 (2014); https://doi.org/10.1016/j.molstruc.2013.10.046
N. Sathya, G. Raja, N.P. Priya and C. Jayabalakrishnan, Appl. Organometal. Chem., 24, 366 (2010); https://doi.org/10.1002/aoc.1621
V.P. Singh and P. Gupta, J. Coord. Chem., 61, 3922 (2008); https://doi.org/10.1080/00958970802160974
B. Oritz and S.M. Park, Bull. Korean Chem. Soc., 21, 405 (2000); https://doi.org/10.5012/bkcs.2000.21.4.405
M. Shakir, O.S.M. Nasman, A.K. Mohamed and S.P. Varkey, Polyhedron, 15, 1283 (1996); https://doi.org/10.1016/0277-5387(95)00379-7
L.S. Chen and S.C. Cummings, Inorg. Chem., 17, 2358 (1978); https://doi.org/10.1021/ic50187a005
R. Atkins, G. Brewer and E. Kokot, G.M. Mockler and E. Sinn, Inorg. Chem., 24, 127 (1985); https://doi.org/10.1021/ic00196a003
M. Kwiatkowski, E. Kwiatkowski, A. Olechnowicz, D.M. Ho and E. Deutsch, J. Chem. Soc., Dalton Trans., 2497 (1990); https://doi.org/10.1039/DT9900002497
A.B.P. Lever, Inorganic Electronic Spectroscopy, NewYork: Elsevier edn. 2 (1984).
W.J. Geary, Coord. Chem. Rev., 7, 122 (1971); https://doi.org/10.1016/S0010-8545(00)80009-0
V.P. Singh, S. Singh, D.P. Singh, K. Tiwari and M. Mishra, J. Mol. Struct., 1058, 71 (2014); https://doi.org/10.1016/j.molstruc.2013.10.046
A. Amiri, M. Amirnasr, S. Meghdadi, K. Mereiter, V. Ghodsi and A. Gholami, Inorg. Chim. Acta, 362, 3934 (2009); https://doi.org/10.1016/j.ica.2009.05.020
V.P. Singh, Spectrochim. Acta A Mol. Biomol. Spectrosc., 71, 17 (2008); https://doi.org/10.1016/j.saa.2007.11.004
D.H. Pereira, F.A.L. Porta, R.T. Santiago, D.R. Garcia and T.C. Ramalho, Revista Virtual de Quimica, 8, 425 (2016); https://doi.org/10.5935/1984-6835.20160032
D. Shin and Y. Jung, Phys. Chem. Chem. Phys., 24, 25740 (2022); https://doi.org/10.1039/D2CP03244A
S. Murugavel, S. Deepa, C. Ravikumar, R. Ranganathan and P. Alagusundaram, J. Mol. Struct., 1222, 128961 (2020); https://doi.org/10.1016/j.molstruc.2020.128961