[1]
Lou, J.; Liu, Z.; Li, Y.; Zhou, M.; Zhang, Z.; Zheng, S.; Wang, R.; Li, J. Synthesis and anti-tumor activities of N′-benzylidene-2-(4-oxothieno[2,3-d]pyrimidin-3(4H)-yl) acetohydrazone derivatives. Bioorg. Med. Chem. Lett., 2011, 21, 6662-6666.
[2]
Kumar, D.; Kumar, N.M.; Ghosh, S.; Shah, K. Novel bis(indolyl)hydrazide-hydrazones as potent cytotoxic agents. Bioorg. Med. Chem. Lett., 2012, 22, 212-215.
[3]
Dandawate, P.; Khan, E.; Padhye, S.; Gaba, H.; Sinha, S.; Deshpande, J.; Swamy, K.V.; Khetmalas, M.; Ahmad, A.; Sarkar, F.H. Synthesis, characterization, molecular docking and cytotoxic activity of novel plumbagin hydrazones against breast cancer cells. Bioorg. Med. Chem. Lett., 2012, 22, 3104-3108.
[4]
Islam, R.; Koizumi, F.; Kodera, Y.; Inoue, K.; Okawara, T.; Masutanid, M. Design and synthesis of phenolic hydrazide hydrazones as potent poly(ADP-ribose) glycohydrolase (PARG) inhibitors. Bioorg. Med. Chem. Lett., 2014, 24, 3802-3806.
[5]
Wei-Yong, L.; Hai-Ying, L.; Bao-Xiang, Z.; Dong-Soo, S.; Song, L.; Jun-Ying, M. Synthesis of novel ribavirin hydrazone derivatives and anti-proliferative activity against A549 lung cancer cells. Carbohydr. Res., 2009, 344, 1270-1275.
[6]
Altıntop, M.D.; Özdemir, A.; Turan-Zitouni, G.; Ilgın, S.; Atlı, Ö.; Işcan, G.; Kaplancıklı, Z.A. Synthesis and biological evaluation of some hydrazone derivatives as new anticandidal and anticancer agents. Eur. J. Med. Chem., 2012, 58, 299-307.
[7]
Nasr, T.; Bondock, S.; Youns, M. Anticancer activity of new coumarin substituted hydrazide-hydrazone derivatives. Eur. J. Med. Chem., 2014, 76, 539-548.
[8]
Congiu, C.; Onnis, V. Synthesis and biological evaluation of novel acylhydrazone derivatives as potential antitumor agents. Bioorg. Med. Chem. Lett., 2013, 20, 6592-6599.
[9]
Mishraa, M.; Tiwari, K.; Shukla, S.; Mishra, R.; Singh, V.P. Synthesis, structural investigation, DNA and protein binding study of some 3D-metal complexes with N′-(phenyl-pyridin-2-yl-methylene)-thiophene-2-carboxylic acid hydrazide. Spectrochim. Acta Part A Mol. Biomol. Spectrosc., 2014, 132, 452-464.
[10]
Chitrapriyaa, N.; Kamatchi, T.S.; Zeller, M.; Leea, H.; Natarajan, K. Synthesis, spectroscopic, crystal structure and DNA binding of Ru (II) complexes with 2-hydroxy-benzoic acid [1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-ethylidene]-hydrazide. Spectrochim. Acta Part A Mol. Biomol. Spectrosc., 2011, 81, 128-134.
[11]
El-Morsy, F.A.; Jean-Claude, B.J.; Butler, I.S.; El-Sayed, S.A.; Mostafa, S.I. Synthesis, characterization and anticancer activity of new zinc(II), molybdate(II), palladium(II), silver(I), rhodium(III), ruthenium(II) and platinum(II) complexes of 5,6-diamino-4-hydroxy-2-mercaptopyrimidine. Inorg. Chim. Acta, 2014, 423, 144-155.
[12]
Mahalingam, V.; Chitrapriya, N.; Fronczek, F.R.; Natarajan, K. New Ru(II)-dmso complexes with heterocyclic hydrazone ligands towards cancer chemotherapy. Polyhedron, 2008, 27, 1917-1924.
[13]
Jayanthi, E.; Kalaiselvi, S.; Padma, V.V.; Bhuvanesh, N.S.P.; Dharmaraj, N. Synthesis, characterization, DNA/protein binding and in vitro cytotoxic evaluation of new Ru(III) complexes containing aroylhydrazone ligands: Does hydrogen bonding influence the coordination behavior of hydrazones? Inorg. Chim. Acta, 2015, 429, 148-159.
[14]
Hosseini-Monfared, H.; Bikas, R.; Mahboubi-Anarjan, P.; Blake, A.J.; Lippolis, V.; Arslan, N.B.; Kazak, C. Oxidovanadium(V) complexes containing hydrazone based O,N,O-donor ligands: Synthesis, structure, catalytic properties and theoretical calculations. Polyhedron, 2014, 69, 90-102.
[15]
Ulukaya, E.; Ari, F.; Dimas, K.; Ikitimur, E.I.; Guney, E.; Yilmaz, V.T. Anti-cancer activity of a novel palladium(II) complex on human breast cancer cells in vitro and in vivo. Eur. J. Med. Chem., 2011, 46, 4957-4963.
[16]
Sathyadevi, P.; Krishnamoorthy, P.; Alagesan, M.; Thanigaimani, K.; Thomas, M.P.; Dharmaraj, N. Synthesis, crystal structure, electrochemistry and studies on protein binding, antioxidant and biocidal activities of Ni(II) and Co(II) hydrazone complexes. Polyhedron, 2012, 31, 294-306.
[17]
Mohareb, R.M.; Al-Omran, F. Reaction of pregnenolone with cyanoacetylhydrazine: Novel synthesis of hydrazide-hydrazone, pyrazole, pyridine, thiazole, thiophene derivatives and their cytotoxicity evaluations. Steroids, 2012, 77, 1551-1559.
[18]
Zining, C.; Ying, L.; Yun, L.; Juan, H.; Jingrong, C.; Ruiqing, W.; Xinling, Y. New class of potent antitumor acylhydrazone derivatives containing furan. Eur. J. Med. Chem., 2010, 45, 5576-5584.
[19]
Altıntop, M.D.; Özdemir, A.; Turan-Zitouni, G.; Ilgın, S.; Atlı, Ö.; İşcan, G.; Kaplancıklı, Z.A. Synthesis and biological evaluation of some hydrazone derivatives as new anticandidal and anticancer agents. Eur. J. Med. Chem., 2012, 58, 299-307.
[20]
Kocyigit-Kaymakcioglu, B.; Oruc-Emre, E.E.; Unsalan, S.; Rollas, S. Antituberculosis activity of hydrazones derived from 4-fluorobenzoic acid hydrazide. Med. Chem. Res., 2009, 18, 277-286.
[21]
Krishnamoorthy, P.; Sathyadevi, P.; Cowley, A.H.; Butorac, R.R.; Dhamaraj, N. Evaluation of DNA binding, DNA cleavage, protein binding and in vitro cytotoxic activities of bivalent transition metal hydrazone complexes. Eur. J. Med. Chem., 2011, 46, 3376-3387.
[22]
Dikmen, M.; Ozturk, N.; Ozturk, Y. The antioxidant potency of punica granatum L. fruit peel reduces cell proliferation and induces apoptosis on breast cancer. J. Med. Food, 2011, 14, 1638-1646.
[23]
Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods, 1993, 65, 55-63.
[24]
Bird, C.; Kirstein, S. Real-time, label-free monitoring of cellular invasion and migration with the xCELLigence system. App. Note Nat. Methods, 2009, 6, 622.
[25]
Solly, K.; Wang, X.; Xu, X.; Strulovici, B.; Zheng, W. Application of real-time cell electronic sensing (RT-CES) technology to cell-based assays. Assay Drug Dev. Technol., 2004, 2, 363-372.
[26]
Urcan, E.; Haertel, U.; Styllou, M.; Hickel, R.; Scherthan, H.; Reichl, F.X. Real-time xCELLigence impedance analysis of the cytotoxicity of dental composite components on human gingival fibroblasts. Dent. Mater., 2010, 26, 51-58.
[27]
Ozkay, Y.; Yurttas, L.; Dikmen, M.; Engür, S. Synthesis and antiproliferative activity evaluation of new thiazole-benzimidazole derivatives using real-time cell analysis (RTCA DP). Med. Chem. Res., 2016, 25, 482-493.
[28]
Dikmen, M.; Cantürk, Z.; Engür, S.; Demirtaş, B.; İlhan, S. Antiangiogenic and antiproliferative effects of halotolerant Penicillium chrysogenum var. chrysogenum on the human umblical vein endothelial cells(HUVECs), IEEE, Xplore. Digital Lib., 2013, 4, 1-4.
[29]
Lee, E.; Koskimaki, J.E.; Pandey, N.B.; Popel, A.S. Inhibition of lymphangiogenesis and angiogenesis in breast tumor xenografts and lymph nodes by a peptide derived from transmembrane protein. Neoplasia, 2013, 15, 112-124.
[30]
Eisenberg, M.C.; Yangjin, K.; Li, R.; Ackerman, W.E.; Kniss, D.A.; Friedman, A. Mechanistic modeling of the effects of myoferlin on tumor cell invasion. Proc. Natl. Acad. Sci., 2011, 108, 20078-20083.
[31]
Liu, W.Y.; Li, H.Y.; Zhao, B.X.; Shin, D.S.; Lian, S.; Miao, J.Y. Synthesis of novel ribavirin hydrazone derivatives and anti-proliferative activity against A549 lung cancer cells. Carbohydr. Res., 2009, 344, 1270-1275.
[32]
Liu, M.; Wang, Y.; Wangyang, W.Z.; Liu, F.; Cui, Y.L.; Duan, Y.S.; Wang, M.; Liu, S.Z.; Rui, C.H. Design, synthesis and insecticidal activities of phtalimides containing a hydrazone substructure. J. Agric. Food Chem., 2010, 58, 6858-6863.
[33]
Ozdemir, Ü.Ö.; Akkaya, N.; Özbek, N. New nickel(II), palladium(II), platinum(II) complexes with aromatic methanesulfonylhydrazone based ligands. Synthesis, spectroscopic characterization and in vitro antibacterial evaluation. Inorg. Chim. Acta, 2013, 400, 13-19.
[34]
Naik, V.M.; Mallur, N.B. Synthesis and characterization of niobium(V) complexes with terdentate ONO donor hydrazones. Indian J. Chem., 2002, 41A, 780-784.
[35]
Jing-lin, W.; Ya-qin, Z.; Bin-sheng, Y. Transition metal complexes of asymmetrical aroyl-hydrazone ligand: Syntheses, structures, DNA binding and cleavage studies. Inorg. Chim. Acta, 2014, 409, 484-496.
[36]
Galal, S.A.; Hegab, K.H.; Kassab, A.S.; Rodriguez, M.L.; Kerwin, S.M.; El-Khamry, A.A.; El Diwani, H.I. New transition metal ion complexes with benzimidazole-5-carboxylic acid hydrazides with antitumor activity. Eur. J. Med. Chem., 2009, 44, 1500-1508.
[37]
Galic, N.; Rubcic, M.; Magdic, ´.K.; Cindric, ´.M.; Tomišic, V. Solution and solid-state studies of complexation of transition-metal cations and Al(III) by aroylhydrazones derived from nicotinic acid hydrazide. Inorg. Chim. Acta, 2011, 366, 98-104.
[38]
Sönmez, M.; Hacıyusufoğlu, M.E. Synthesis, characterization and antimicrobial studies of Cu(II), Co(II), Ni(II) and Zn(II) Schiff base complexes derived from acetylacetone with 1-amino-5-benzoyl-4-phenyl-1H-pyrimidine-2-one. Asian J. Chem., 2006, 18, 2032-2036.
[39]
McCauley, J.; Zivanovic, A.; Skropeta, D. Bioassays for anticancer activities. Methods Mol. Biol., 2013, 1055, 191-205.
[40]
Martinez-Serra, J.; Gutierrez, A.; Muñoz-Capó, S.; Navarro-Palou, M.; Ros, T.; Amat, J.C.; Lopez, B.; Marcus, T.F.; Fueyo, L.; Suquia, A.G.; Gines, J.; Rubio, F.; Ramos, R.; Besalduch, J. xCELLigence system for real-time label-free monitoring of growth and viability of cell lines from hematological malignancies. OncoTargets Ther., 2014, 7, 985-994.
[41]
Moniri, M.R.; Young, A.; Reinheimer, K.; Rayat, J.; Dai, L.J.; Warnock, G.L. Dynamic assessment of cell viability, proliferation and migration using real time cell analyzer system (RTCA). Cytotechnology, 2015, 67, 379-386.
[42]
Dowling, C.; Herranz, M.; Ors, C.; Kiely, P.A. Using real-time impedance-based assays to monitor the effects of fibroblast-derived media on the adhesion, proliferation, migration and invasion of colon cancer cells. Biosci. Rep., 2014, 34, 415-417.
[43]
Moe, B.; Gabos, S.F.; Li, X. Real-time cell-microelectronic sensing of nanoparticle-induced cytotoxic effects. Anal. Chim. Acta, 2013, 789, 83-90.