Copyright (c) 2018 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Quinazolinone Platinum Metal Complexes: in silico Design, Synthesis and Evaluation of Anticancer Activity
Corresponding Author(s) : Sanjay D. Sawant
Asian Journal of Chemistry,
Vol. 30 No. 10 (2018): Vol 30 Issue 10, 2018
Abstract
Dihydrofolate reductase (DHFR) has been explored as a target for the development of agents for wide variety of human diseases, including cancer, autoimmune and infectious diseases. Several metal complexes are being used in management of cancer. The square planar Pt(II) complex, cis PtCl2(NH3)2 turned out to be even more effective at forcing filamentous growth. Cisplatin is an inorganic heavy metal complex that has activity similar to cell-cycle-phase-nonspecific alkylating agents such as cyclophosphamide and some other Ni and Cu metal complexes. It produces intrastrand DNA cross-link and form DNA adducts, thus inhibiting the synthesis of DNA, RNA and proteins preferentially. in silico Screening of platinum metal complexes was performed by Vlife MDS 4.3 software. In this procedure, selection of molecule, selection of PDB, optimization of PDB and docking of molecules was carried out. Synthesis of metal complexes was done by multi component reaction method. Platinum metal complexes of quinazolinone Schiff bases prioritized by in silico studies were characterized by IR, TLC, NMR, XRD, FESEM and some physico-chemical parameters. Prioritized molecules were further evaluated by in vitro anticancer cell line assay on ten cell lines with adriamycin as standard. The results showed that the platinum metal complexes of qunazolinone Schiff bases can be potential anticancer agents through DHFR inhibitory mechanism.
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- A.G. Nerkar and M. Sahu, J. Pharm. Pharm. Sci., 6, 509 (2014).
- National Cancer Control Programmes, Policies and Managerial Guidelines, World Health Organization, Geneva, edn 2 (2002).
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References
A.G. Nerkar and M. Sahu, J. Pharm. Pharm. Sci., 6, 509 (2014).
National Cancer Control Programmes, Policies and Managerial Guidelines, World Health Organization, Geneva, edn 2 (2002).
K.A. Dinshaw, D.N. Rao and B. Ganesh, Tata Memorial Hospital Cancer Registry Annual Report, Mumbai, India (1999).
H.-L. Ng, X. Ma, E.-H. Chew and W.-K. Chui, J. Med. Chem., 60, 1734 (2017); https://doi.org/10.1021/acs.jmedchem.6b01253.
J. Jolivet, K.H. Cowan, G.A. Curt, N.J. Clendninn and B.A. Chabner, N. Engl. J. Med., 309, 1094 (1983); https://doi.org/10.1056/NEJM198311033091805.
Y. Takemura, H. Kobayashi and H. Miyachi, Anticancer Drugs, 10, 677 (1999); https://doi.org/10.1097/00001813-199908000-00008.
N. Gonen and Y.G. Assaraf, Drug Resist. Updat., 15, 183 (2012); https://doi.org/10.1016/j.drup.2012.07.002.
E. Hamel, C.M. Lin, J. Plowman, H.-K. Wang, K.-H. Lee and K. D. Paull, Biochem. Pharmacol., 51, 53 (1996); https://doi.org/10.1016/0006-2952(95)02156-6.
K.B. Gudasi, S.A. Patil, M.V. Kulkarni and M. Nethaji, Transition Met. Chem., 34, 325 (2009); https://doi.org/10.1007/s11243-009-9198-8.
N. Farrell, Drugs Chemother Agents, 11, 809 (1989).
P.R. Mitchell and H. Sigel, Eur. J. Biochem., 88, 149 (1978); https://doi.org/10.1111/j.1432-1033.1978.tb12432.x.
http://nihserver.mbi.ucla.edu/SAVES.
H.M. Berman, Nucleic Acids Res., 28, 235 (2000); https://doi.org/10.1093/nar/28.1.235.
N.C. Desai, A. Dodiya, N. Shihory, J. Saudi Chem. Soc., 17, 259 (2013); https://doi.org/10.1016/j.jscs.2011.04.001.
A.S. Wheeler and W.M. Oates, J. Am. Chem. Soc., 32, 770 (1910); https://doi.org/10.1021/ja01924a009.
A.G. Nerkar, A.K. Saxena, S.A. Ghone and A.K. Thaker, E-J. Chem., 6(s1), S97 (2009); https://doi.org/10.1155/2009/506576.
K.T. Potts, M. Cipullo, P. Ralli and G. Theodoridis, J. Am. Chem. Soc., 103, 3584 (1981); https://doi.org/10.1021/ja00402a061.
K.S. Prasad, L.S. Kumar, S. Chandan, H.D. Revanasiddappa and B. Vijaya, Anal. Univ. Bucuresti Chim., 20, 7 (2011).
J. Barretina, G, Caponigro, N. Stransky, K. Venkatesan, A.A. Margolin, S. Kim, C.J. Wilson, J. Lehár, G.V. Kryukov, D. Sonkin, A. Reddy, M. Liu, L. Murray, M.F. Berger, J.E. Monahan, P. Morais, J. Meltzer, A. Korejwa, J. Jané-Valbuena, F.A. Mapa, J. Thibault, E. Bric-Furlong, P. Raman, A. Shipway, I.H. Engels, J. Cheng, G.K. Yu, J. Yu, P. Aspesi, Jr., M. de Silva, K. Jagtap, M.D. Jones, L. Wang, C. Hatton, E. Palescandolo, S. Gupta, S. Mahan, C. Sougnez, R.C. Onofrio, T. Liefeld, L. MacConaill, W. Winckler, M. Reich, N. Li, J.P. Mesirov, S.B. Gabriel, G. Getz, K. Ardlie, V. Chan, V.E. Myer, B.L. Weber, J. Porter, M. Warmuth, P. Finan, J.L. Harris, M. Meyerson, T.R. Golub, M.P. Morrissey, W.R. Sellers, R. Schlegel and L.A. Garraway, Nature, 483, 603 (2012); https://doi.org/10.1038/nature11003.
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