A mononuclear copper(II) complex based on the polypyridyl ligand 2,4,6-tris(2-pyridyl)-1,3,5-triazine (tptz), [Cu(tptz)2] 2+: X-ray crystal structure, DNA binding and in vitro cell cytotoxicity

Polyhedron

Volumn 44, Issue 1, 2012, Pages 101-112

  Abdi, Khatereh ^a   Hadadzadeh, Hassan ^a   Salimi, Mona ^b   Simpson, Jim ^c   Khalaji, Aliakbar Dehno ^d  

^a ISFAHAN UNIVERSITY OF TECHNOLOGY   (Iran)

^b PASTEUR INSTITUTE OF IRAN   (Iran)

^c UNIVERSITY OF OTAGO   (New Zealand)

^d GOLESTAN UNIVERSITY   (Iran)

Author keywords

2,4,6 Tris(2 pyridyl) 1,3,5 triazine (tptz); Cell cytotoxicity; Copper(II) complex; DNA binding; X ray crystallography

Indexed keywords

CELL CULTURE; CELLS; COPPER COMPOUNDS; CRYSTAL STRUCTURE; CYTOTOXICITY; DNA; ELECTROPHORESIS; LIGANDS; SELF ASSEMBLY; SINGLE CRYSTALS; SPECTROSCOPIC ANALYSIS;

2,4,6-TRIS(2-PYRIDYL)-1,3,5-TRIAZINE (TPTZ); CELL CYTOTOXICITY; COPPER(II) COMPLEX; DNA-BINDING; IN-VITRO; MONONUCLEAR COPPER; POLYPYRIDYL LIGANDS; PYRIDYL; VITRO CYTOTOXICITIES; X RAY CRYSTAL STRUCTURES;

X RAY CRYSTALLOGRAPHY;

EID: 84864947301     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.poly.2012.06.089     Document Type: Article

References (87)

1. M. Chauhan, K. Banerjee, and F. Arjmand Inorg. Chem. 46 2007 3072
2. G.-J. Chen, X. Qiao, P.-Q. Qiao, G.-J. Xu, J.-Y. Xu, J.-L. Tian, W. Gu, X. Liu, and S.-P. Yan J. Inorg. Biochem. 105 2011 119
3. C.X. Zhang, and S.J. Lippard Curr. Opin. Chem. Biol. 7 2003 481
4. F.R. Keene, J.A. Smith, and J.G. Collins Coord. Chem. Rev. 253 2009 2021
5. A.N. Wein, A.T. Stockhausen, K.I. Hardcastle, M.R. Saadein, S. Peng, D. Wang, D.M. Shin, Z. Chen, and J.F. Eichler J. Inorg. Biochem. 105 2011 663
6. C. Deegan, M. McCann, M. Devereux, B. Coyle, and D.A. Egan Cancer Lett. 247 2007 224
7. A. Barve, A. Kumbhar, M. Bhat, B. Joshi, R. Butcher, U. Sonawane, and R. Joshi Inorg. Chem. 48 2009 9120
8. P.C. Bruijnincx, and P.J. Sadler Curr. Opin. Chem. Biol. 12 2008 197
9. K. Ghosh, P. Kumar, N. Tyagi, U.P. Singh, and N. Goel Inorg. Chem. Commun. 14 2011 489
10. S. Dhar, D. Senapati, P.K. Das, P. Chattopadhyay, M. Nethaji, and A.R. Chakravarty J. Am. Chem. Soc. 125 2003 12118
11. Y. Wang, and J.-F. Chiu Met. Based Drugs 2008 2008 1
12. A.M. Pizarro, and P.J. Sadler Biochimie 91 2009 1198
13. E. Meggers Curr. Opin. Chem. Biol. 11 2007 287
14. N. Farrell Coord. Chem. Rev. 232 2002 1
15. G. Zuber, J.C. Quada, and S.M. Hecht J. Am. Chem. Soc. 120 1998 9368
16. Q.-Y. Chen, H.-J. Fu, W.-H. Zhu, Y. Qi, Z.-P. Ma, K.-D. Zhao, and J. Gao Dalton Trans. 40 2011 4414
17. M. Chandra, A.N. Sahay, D.S. Pandey, R.P. Tripathi, J.K. Saxena, V.J.M. Reddy, M.C. Puerta, and P. Valerga J. Organomet. Chem. 689 2004 2256
18. R. Shen, P. Wang, and N. Tang J. Fluoresc. 20 2010 1287
19. U. Chaveerach, A. Meenongwa, Y. Trongpanich, C. Soikum, and P. Chaveerach Polyhedron 29 2010 731
20. P. Kumar, A.K. Singh, J.K. Saxena, and D.S. Pandey J. Organomet. Chem. 694 2009 3570
21. R.N. Jadeja, K.M. Vyas, V.K. Gupta, R.G. Joshi, and C.R. Prabha Polyhedron 31 2012 767
22. H.-K. Liu, and P.J. Sadler Acc. Chem. Res. 44 2011 349
23. M.N. Patel, P.A. Dosi, and B.S. Bhatt Spectrochim. Acta A86 2012 508
24. S. Rubino, P. Portanova, A. Girasolo, G. Calvaruso, S. Orecchio, and G.C. Stocco Eur. J. Med. Chem. 44 2009 1041
25. K. Palanichamy, N. Sreejayan, and A.C. Ontko J. Inorg. Biochem. 106 2012 32
26. J. Chen, X. Wang, Y. Shao, J. Zhu, Y. Zhu, Y. Li, Q. Xu, and Z. Guo Inorg. Chem. 46 2007 3306 and references therein
27. L. Zhang, X.-Q. Lü, Q. Zhang, C.-L. Chen, and B.-S. Kang Transition Met. Chem. 30 2005 76
28. P. Byers, G.Y.S. Chan, M.G.B. Drew, M.J. Hudson, and C. Madic Polyhedron 15 1996 2845
29. H. Hadadzadeh, M. Maghami, J. Simpson, A.D. Khalaji, and K. Abdi J. Chem. Crystallogr. 2012 10.1007/s10870-012-0296-7
30. S.K. Singh, S. Sharma, M. Chandra, and D.S. Pandey J. Organomet. Chem. 690 2005 3105
31. P. Kumar, A.K. Singh, R. Pandey, and D.S. Pandey J. Organomet. Chem. 696 2011 3454
32. S. Rubino, P. Portanova, A. Albanese, G. Calvaruso, S. Orecchio, G. Fontana, and G.C. Stocco J. Inorg. Biochem. 101 2007 1473
33. R.N. Patel, N. Singh, K.K. Shukla, V.L.N. Gundla, and U.K. Chauhan Spectrochim. Acta A63 2006 21
34. D.S. Sigman, D.R. Graham, V. D'Aurora, and A.M. Stern J. Biol. Chem. 254 1979 12269
35. Y.-L. Song, Y.-T. Li, and Z.-Y. Wu J. Inorg. Biochem. 102 2008 1691
36. S. Apelgot, J. Coppey, A. Fromentin, E. Guille, M.F. Poupon, and A. Roussel Anticancer Res. 6 1986 159
37. C. Marzano, M. Pellei, F. Tisato, and C. Santini Anti-Cancer Agents Med. Chem. 9 2009 185
38. V. Rajendiran, R. Karthik, M. Palaniandavar, H. Stoeckli-Evans, V.S. Periasamy, M.A. Akbarsha, B.S. Srinag, and H. Krishnamurthy Inorg. Chem. 46 2007 8208
39. C.H. Ng, K.C. Kong, S.T. Von, P. Balraj, P. Jensen, E. Thirthagiri, H. Hamada, and M. Chikira Dalton Trans. 2008 447
40. M. Navarro, E.J. Cisneros-Fajardo, M. Fernandez-Mestre, D. Arrieche, and E. Marchan J. Inorg. Biochem. 97 2003 364
41. M. Navarro, E.J. Cisneros-Fajardo, A. Sierralta, M. Fernández- Mestre, P. Silva, D. Arrieche, and E. Marchán J. Biol. Inorg. Chem. 8 2003 401
42. S. Rajalakshmi, T. Weyhermüller, A.J. Freddy, H.R. Vasanthi, and B.U. Nair Eur. J. Med. Chem. 46 2011 608
43. Q.-Y. Chen, H.-J. Fu, J. Huang, and R.-X. Zhang Spectrochim. Acta A75 2010 355
44. K. Abdi, H. Hadadzadeh, M. Weil, and M. Salimi Polyhedron 31 2012 638
45. G.M. Sheldrick Sadabs, A Program for Empirical Absorption and Other Corrections 1997 University of Göttingen Germany
46. G.M. Sheldrick Acta Crystallogr., Sect. A 64 2008 112
47. M.F. Reichmann, S.A. Rice, C.A. Thomas, and P. Doty J. Am. Chem. Soc. 76 1954 3047
48. J. Marmur J. Mol. Biol. 3 1961 208
49. T. Mosmann J. Immunol. Methods 65 1983 55
50. J.-V. Folgado, W. Henke, R. Allmann, H. Stratemeier, D. Beltrán-Porter, T. Rojo, and D. Reinen Inorg. Chem. 29 1990 2035
51. T. Glaser, T. Lügger, and R. Fröhlich Eur. J. Inorg. Chem. 2004 394
52. Y.-Q. Zheng, W. Xu, F. Lin, and G.-S. Fang J. Coord. Chem. 59 2006 1825
53. M.G.B. Drew, M.J. Hudson, P.B. Iveson, M.L. Russell, and C. Madic Acta Crystallogr., Sect. C 54 1998 985
54. A. Majumder, V. Gramlich, G.M. Rosair, S.R. Batten, J.D. Masuda, M.S. El Fallah, J. Ribas, J.-P. Sutter, C. Desplanches, and S. Mitra Cryst. Growth Des. 6 2006 2355
55. M.C. Aragoni, M. Arca, F.A. Devillanova, M.B. Hursthouse, S.L. Huth, F. Isaia, V. Lippolis, A. Mancini, S. Soddu, and G. Verani Dalton Trans. 2007 2127
56. H. Hadadzadeh, S.R. Hosseinian, and S.J.A. Fatemi Polyhedron 28 2009 2776
57. R.J. Deeth, A. Anastasi, C. Diedrich, and K. Randell Coord. Chem. Rev. 253 2009 795
58. B. Kozlevčar, A. Golobič, and P. Strauch Polyhedron 25 2006 2824
59. H. Saravani, A.R. Rezvani, H. Hadadzadeh, and N. Safari Iran. J. Chem. Chem. Eng. 26 2007 103
60. F.H. Allen, and W.D.S. Motherwell Acta Crystallogr., Sect. B 58 2002 407
61. A.B.P. Lever Inorganic Electronic Spectroscopy second ed. 1984 Elsevier Amsterdam
62. K. Nakamato Infrared and Raman Spectra of Inorganic and Coordination Compounds: Part II. Application in Coordination, Organometallic and Bioinorganic Chemistry sixth ed. 2009 Wiley-Interscience New York
63. F.Q. Liu, Q.X. Wang, K. Jiao, F.F. Jian, G.Y. Liu, and R.X. Li Inorg. Chim. Acta 359 2006 1524
64. D.-D. Li, J.-L. Tian, W. Gu, X. Liu, and S.-P. Yan Eur. J. Inorg. Chem. 2009 5036
65. D. Mandal, M. Chauhan, F. Arjmand, G. Aromí, and D. Ray Dalton Trans. 2009 9183
66. C. Tu, Y. Shao, N. Gan, Q. Xu, and Z. Guo Inorg. Chem. 43 2004 4761
67. R.S. Sancheti, R.S. Bendre, and A.A. Kumbhar Polyhedron 31 2012 12
68. A. Pal, B. Biswas, S.K. Mondal, C.-H. Lin, and R. Ghosh Polyhedron 31 2012 671
69. D. Li, J. Tian, Y. Kou, F. Huang, G. Chen, W. Gu, X. Liu, D. Liao, P. Cheng, and S. Yan Dalton Trans. 2009 3574
70. S. Mathur, and S. Tabassum Biometals 21 2008 299
71. X.-L. Wang, H. Chao, B. Peng, and L.-N. Ji Transition Met. Chem. 32 2007 125
72. J.R. Lakowicz, and G. Weber Biochemistry 12 1973 4161
73. Q.X. Wang, F. Gao, and K. Jiao Electroanalysis 20 2008 2096
74. E. Grueso, G. López-Pérez, M. Castellano, and R. Prado-Gotor J. Inorg. Biochem. 106 2012 1
75. M.T. Carter, M. Rodriguez, and A.J. Bard J. Am. Chem. Soc. 111 1989 8901
76. A.D. Richards, and A. Rodger Chem. Soc. Rev. 36 2007 471
77. R. Senthil Kumar, K. Sasikala, and S. Arunachalam J. Inorg. Biochem. 102 2008 234
78. C.K.-L. Li, R.W.-Y. Sun, S.C.-F. Kui, N. Zhu, and C.-M. Che Chem. Eur. J. 12 2006 5253
79. C.W. Yde, and O.-G. Issinger Int. J. Oncol. 29 2006 1397
80. K. Ghosh, P. Kumar, N. Tyagi, U.P. Singh, N. Goel, A. Chakraborty, P. Roy, and M.C. Baratto Polyhedron 30 2011 2667
81. A. Chakraborty, P. Kumar, K. Ghosh, and P. Roy Eur. J. Pharmacol. 647 2010 1
82. X. Zhao, S.C.J. Loo, P.P.-F. Lee, T.T.Y. Tan, and C.K. Chu J. Inorg. Biochem. 104 2010 105
83. S. Gama, F. Mendes, F. Marques, I.C. Santos, M.F. Carvalho, I. Correia, J.C. Pessoa, I. Santos, and A. Paulo J. Inorg. Biochem. 105 2011 637
84. D. Kovala-Demertzi, M. Staninska, I. Garcia-Santos, A. Castineiras, and M.A. Demertzis J. Inorg. Biochem. 105 2011 1187
85. F.A. Beckford, J. Thessing, A. Stott, A.A. Holder, O.G. Poluektov, L. Li, and N.P. Seeram Inorg. Chem. Commun. 15 2012 225
86. P. Shi, M. Lin, J. Zhu, Y. Zhang, and Q. Jiang J. Biochem. Mol. Toxicol. 23 2009 295
87. S. Patitungkho, S. Adsule, P. Dandawate, S. Padhye, A. Ahmad, and F.H. Sarkar Bioorg. Med. Chem. Lett. 21 2011 1802