L. Nemati, H. Keypour, N. Shahabadi et al.
Journal of Molecular Liquids 337 (2021) 116292
copper complexes with calf thymus DNA. Eur. J. Chem. 4 (2006) 502–522.
[5] P.M. Takahara, C.A. Frederick, S.J. Lippard, Crystal structure of the anticancer
drug cisplatin bound to duplex DNA, J Am Chem Soc 118 (1996) 12309–12321,
[6] P.J. Loehrer, L.H. Einhorn, Drugs five years later. Cisplatin, Ann. Intern. Med.
[7] Α. Garoufis, S.K. Hadjikakou, N. Hadjiliadis, Palladium coordination compounds
as anti-viral, anti-fungal, anti-microbial and anti-tumor agents, Coord. Chem.
[8] S. Medici, M. Peana, V.M. Nurchi, J.I. Lachowicz, G. Crisponi, M.A. Zoroddu,
Metals in Medicine: Latest Advances Coord, Chem. Rev. 284 (2015) 329–350,
Synthesis of some Co(II), Ni(II), Cu(II) and Zn(II) complexes and crystal
structure and theoretical studies, J. Mol. Struct. 1115 (2016) 180–186, https://
[28] H. Keypour, M. Mahmoudabadi, A. Shooshtari, M. Bayat, R. Karamian, M.
Asadbegy, R.W. Gable, Synthesis, crystal structure, theoretical studies and
biological properties of three novel trigonal prismatic Co(II), Ni(II) and Cu(II)
macroacyclic Schiff base complexes incorporating piperazine moiety, Inorg.
[29] H. Keypour, N. Rahpeyma, M. Rezaeivala, P. Arzhangi, M. Bayat, L. Valencia, Y.
Elerman, O. Büyükgüngör, Synthesis and structural characterization of a new
Schiff base macrocyclic ligand containing a piperazine head unit and its metal
complexes. Crystal structure of the Co(II) complex, Polyhedron. 51 (2013)
[9] W. Wang, Z. Guo, Targeting and delivery of platinum-based anticancer drugs,
[10] M. Rezaeivala, H. Keypour, Schiff base and non-Schiff base macrocyclic ligands
and complexes incorporating the pyridine moiety – The first 50 years, Coord.
[11] B.K. Panda, A. Chakravorty, Carbonylation of four-membered ruthenium and
osmium metallacycles incorporating an orthometallated phenolic function:
New acylruthenium and arylosmium complexes, J. Organomet. Chem. 690
[30] H. Keypour, M. Rezaeivala, M. Mirzaei-Monsef, K. Sayin, N. Dilek, H. Unver,
Synthesis and characterization of Co(II), Ni(II), Cu(II) and Zn(II) complexes
with a new homopiperazine macrocyclic Schiff base ligand, Inorg. Chim. Acta.
[31] H.M. Niemeyer, Conformational equilibria in six-membered rings, J. Mol.
[32] H. Keypour, M. Rezaeivala, L. Valencia, P. Pérez-Lourido, Synthesis and crystal
structure of Mn(II) complexes with novel macrocyclic Schiff-base ligands
[12] K.R. Krishnapriya, M. Kandaswamy, Coordination properties of
a
dicompartmental ligand with tetra- and hexadentate coordination sites
towards copper (II) and nickel (II) ions, Polyhedron 24 (2005) 113–120,
[33] J. Marmur, A procedure for the isolation of deoxyribonucleic acid from micro-
[13] K.N. Kumar, R. Ramesh, Synthesis of lanthanide(III) complexes of chloro- and
bromo substituted 18-membered tetraaza macrocycles, Polyhedron 18 (1999)
[34] M.E. Reichmann, S.A. Rice, C.A. Thomas, P. Doty, A Further Examination of the
Molecular Weight and Size of Desoxypentose Nucleic Acid, J. Am. Chem. Soc.
[14] H. Keypour, N. Ansari, M. Mahmoudabadi, R. Karamian, S.H.M. Farida, M.E.
Moghadam, R.W. Gable, Mn(III), Zn(II) and Pt(II) macroacyclic complexes:
Synthesis, X-ray structures, anticancer and antioxidant activities, J. Inorganica
[15] P. Das, W. Linert, Schiff base-derived homogeneous and heterogeneous
palladium catalysts for the Suzuki-Miyaura reaction, Coord. Chem. Rev. 311
[16] P. Rathelot, P. Vanelle, M. Gasquet, F. Delmas, M.P. Crozet, P. Timon-David, J.
Maldonado, Synthesis of novel functionalized 5-nitroisoquinolines and
evaluation of in vitro antimalarial activity, Eur. J. Med. Chem. 30 (1995)
[35] N. Shahabadi, L. Heidari Synthesis, characterization and multi-spectroscopic
DNA interaction studies of a new platinum complex containing the drug
metformin. Spectrochimica Acta Part A: Molecular and Biomolecular
[36] G.M. Morris, R. Huey, W. Lindstrom, M.F. Sanner, R.K. Belew, D.S. Goodsell, A.J.
Olson, AutoDock4 and AutoDockTools4: Automated docking with selective
[37] G.M. Morris, R. Huey, A.J. Olson, Using Auto Dock for ligand-receptor docking,
Curr. Protoc. Bioinf.
0471250953.bi0814s24.
[17] H. Keypour, M.T. Rezaei, M. Jamshidi, S. H. M, Farida, R, Karamian, Synthesis,
cytotoxicity, and antioxidant activity by in vitro and molecular docking studies
of asymmetrical diamine containing piperazine moiety and related Zn(II), Cd
(II) and Mn(II) macrocyclic schif base complexes, J. Inorg. Chem. Commun.125
[38] W.L. DeLano, The PyMOL Molecular Graphics System, DeLano Scientific, San
Carlos, CA, USA, 2004. <http://pymol.sourceforge.net/>.
[39] Y. Luo, F. Xiao, S. Qian, W. Lu, B. Yang, Synthesis and in vitro cytotoxic
evaluation of some thiazolylbenzimidazole derivatives, Eur. J. Med. Chem. 46
[18] Y.H. Ebead, H.M. Salman, M.A. Abdellah, Experimental and theoretical
investigations of spectral, tautomerism and acid-base properties of Schiff
bases derived from some amino acids, Bull. Korean. Chem. Soc. 31 (2010) 850–
[19] B. Iftikhar, J. Kanwal, M. S. U. Khan, Z. Akhter, B. Mirza, V. Mckee ,Synthesis,
character- rization and biological assay of Salicylaldehyde Schiff base Cu(II)
org/10.1016/j.molstruc.2017.11.022.
[20] M.M. Omar, G.G. Mohamed, A.A. Ibrahim, Spectroscopic characterization of
metal complexes of novel Schiff base. Synthesis, thermal and biological
activity studies, Spectrochim. Acta A Mol. Biomol. Spectrosc. 73 (2009) 358–
[21] F.-U. Rahman, A. Ali, I.U. Khan, H.-Q. Duong, S.-B. Yu, Y.-J. Lin, H. Wang, Z.-T. Li,
D.-W. Zhang, Morpholine or methylpiperazine and salicylaldimine based
heteroleptic square planner platinum (II) complexes: In vitro anticancer study
and growth retardation effect on E. coli, Eur. J. Med. Chem. 131 (2017) 263–
[22] H. Keypour, M. Shayesteh, A. Sharifi-Rad, S. Salehzadeh, H. Khavasi, L. Valencia,
Synthesis and characterization of copper(II) and cobalt(II) complexes with two
new potentially hexadentate Schiff base ligands. X-ray crystal structure
determination of one copper(II) complex, J. Organomet. Chem. 693 (2008)
[23] H. Keypour, R. Azadbakht, S. Salehzadeh, H. Khanmohammadi, H. Khavasi, H.
Adams, Synthesis, crystal structure and spectroscopic properties of some
cadmium(II) complexes with three polyamine and corresponding
macroacyclic Schiff base ligands, J. Organomet. Chem. 693 (2008) 2237,
[24] H. Keypour, M. Rezaeivala, L. Valencia, P. Pérez-Lourido, H.R. Khavasi,
Synthesis and characterization of some new Co(II) and Cd(II) macroacyclic
Schiff-base complexes containing piperazine moiety, Polyhedron 28 (2009)
[25] H. Keypour, M. Rezaeivala, L. Valencia, S. Salehzadeh, P. Pérez-Lourido, H.R.
Khavasi, Synthesis and crystal structure of some new cadmium (II)
macrocyclic Schiff-base complexes containing piperazine moiety, Polyhedron
[40] H. Keypour, F. Forouzandeh, S. Salehzadeh, F. Hajibabaei, S. Feizi, R. Karamian,
N. Ghiasi, R. W. Gable, DNA binding studies and antibacterial properties of a
new Schiff base ligand containing homopiperazine and products of its reaction
with Zn(II), Cu(II) and Co(II) metal ions: X-ray crystal structure of Cu(II) and Zn
poly.2019.06.023.
[41] J.H. Price, A.N. Williamson, R.F. Schramm, B.B. Wayland, Palladium(I1) and
Platinum(I1) Alkyl Sulfoxide Complexes. Examples of Sulfur-Bonded, Mixed
Sulfur and Oxygen-Bonded, and Totally Oxygen-Bonded Complexes, J. Inorg.
[42] O.V. Dolomanov, L.J. Bourhis, R.J. Gildea, J.A.K. Howard, H. Puschmann, OLEX2:
a complete structure solution, refinement and analysis program, J. Appl. Cryst.
[43] G.M. Sheldrick, SHELXT– Integrated space-group and crystal-structure
determination, Acta Cryst.
[44] G.M. Sheldrick, Crystal structure refinement with SHELXL, Acta Cryst. C 71
[45] D. Tran Buu, V. Duong Ba, M. Khoi Nguyen Hoang, T. Vu Quoc, L. Duong Khanh,
Y. Oanh Doan Thi, L. Van Meervelt, Synthesis and redetermination of the
crystal structure of salicylaldehyde N (4)-morpholinothiosemicarbazone, Acta.
[46] N.S. Gill, R.H. Nutall, D.E. Scaife, The infra-red spectra of pyridine complexes
[47] R. Melanson, F.D. Rochon, trans-Bis(tert-butylamine)dichloroplatinum(II),
C8H22Cl2N2Pt, Acta Cryst. Sect.C: Struct. Commun. 41(1985) 350-352.
[48] E.C. Long, J.K. Barton, On demonstrating DNA intercalation, Acc. Chem. Res. 23
[49] Y.J. Liu, X.Y. We, F.H. Wu, W.J. Mei, L.X. He, Interaction studies of DNA binding
of ruthenium (II) mixedligand complexes: [Ru(phen)2(dtmi)]2+and [Ru (phen)2
(dtni)]2+
,
Spectrochim. Acta Part
[50] R. Marty, N.Ch. Nsoukpoe-Kossi, D. Charbonneau, C.M. Weinert, L. Kreplak, H.A.
Tajmir-Riahi, Structural analysis of DNA complexation with cationic lipids,
[51] K.Y. Choi, Synthesis, properties and X-ray crystal structures of nickel(II)
complexes of hexaazamacrotetracyclic ligand, J. Coord. Chem. 56 (2010) 481–
[26] H. Keypour, M. Rezaeivala, L. Valencia, P. Pérez-Lourido, A.H. Mahmoudkhani,
Synthesis and characterization of two zinc(II) macrocyclic Schiff-base
complexes containing piperazine moiety, crystal structure of one complex,
[27] H. Keypour, M. Rezaeivala, A. Ramezani-Aktij, M. Bayat, N. Dilek, H. Ünver,
New macrocyclic schiff base complexes incorporating a homopiperazine unit:
11