Metal based pharmacologically active agents: Synthesis, structural characterization, molecular modeling, CT-DNA binding studies and in vitro antimicrobial screening of iron(II) bromosalicylidene amino acid chelates

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 117, Issue , 2014, Pages 366-378

  Abdel Rahman, Laila H ^a   El Khatib, Rafat M ^a   Nassr, Lobna A E ^a   Abu Dief, Ahmed M ^a   Ismael, Mohamed ^a   Seleem, Amin Abdou ^a  

^a Sohag University   (Egypt)

Author keywords

Antimicrobial; Calf thymus DNA; Fe(II) chelates; Gel electrophoresis; Molecular modeling; Schiff bases

Indexed keywords

AGAROSE GEL ELECTROPHORESIS; ANTIBACTERIAL AND ANTIFUNGAL ACTIVITY; ANTIMICROBIAL; CALF THYMUS DNA; GEL ELECTROPHORESIS; MAGNETIC SUSCEPTIBILITY MEASUREMENTS; SCHIFF BASIS; STRUCTURAL CHARACTERIZATION;

AMINO ACIDS; ANTIMICROBIAL AGENTS; ASPERGILLUS; BACTERIA; CHELATION; DNA; ELECTROPHORESIS; ESCHERICHIA COLI; IRON COMPOUNDS; LIGANDS; MAGNETIC SUSCEPTIBILITY; METAL COMPLEXES; MOLECULAR MODELING; QUANTUM THEORY; SYNTHESIS (CHEMICAL); THERMOGRAVIMETRIC ANALYSIS; THYMUS;

COMPLEXATION;

AMINO ACID; ANTIINFECTIVE AGENT; BROMOSALICYLIC ACID ISOPROPYLAMIDE; CALF THYMUS DNA; CHELATING AGENT; COORDINATION COMPOUND; DNA; FERROUS ION; SALICYLIC ACID DERIVATIVE; SCHIFF BASE;

AGAR GEL ELECTROPHORESIS; ANIMAL; ARTICLE; BACTERIUM; CATTLE; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECT; FE(II) CHELATES; FUNGUS; GEL ELECTROPHORESIS; IN VITRO STUDY; INFRARED SPECTROPHOTOMETRY; METABOLISM; MOLECULAR MODEL;

ANTIMICROBIAL; CALF THYMUS DNA; FE(II) CHELATES; GEL ELECTROPHORESIS; MOLECULAR MODELING; SCHIFF BASES;

AMINO ACIDS; ANIMALS; ANTI-INFECTIVE AGENTS; BACTERIA; CATTLE; CHELATING AGENTS; COORDINATION COMPLEXES; DNA; ELECTROPHORESIS, AGAR GEL; FERROUS COMPOUNDS; FUNGI; MODELS, MOLECULAR; MOLECULAR STRUCTURE; SALICYLATES; SCHIFF BASES; SPECTROPHOTOMETRY, INFRARED;

EID: 84883201639     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2013.07.056     Document Type: Article

References (79)

1. Y. Prashanthi, K. Kiranmai, N.J.P. Subhashini, and S. Shivaraj Spectrochim. Acta A 70 1 2008 30 35
2. V.P. Daniel, B. Murukan, B.S. Kumari, and K. Mohanan Spectrochim. Acta A 70 2 2008 403 410
3. S.A. Galal, K.H. Hegab, A.S. Kassab, M.L. Rodriguez, S.M. Kerwin, A.A. El-Khamry, and H.I. El Diwani Eur. J. Med. Chem. 44 4 2009 1500 1508
4. J.G.H. Du Preez, T.I.A. Gerber, P.J. Fourie, and J. Van Wyk J. Coord. Chem. 13 1984 173 178
5. Z.L. You, H.L. Zhu, and W.S.Z. Liu Anorg. Allg. Chem. 630 2004 1617 1622
6. K. Ghosh, N. Tyagi, P. Kumar, U.P. Singh, and N. Goel J. Inorg. Biochem. 104 2010 9 18
7. S.M. Abdallah, G.G. Mohamed, M.A. Zayed, and M.S. Abou El-Ela Spectrochim. Acta A 73 5 2009 833 840
8. Y.C. Liu, and Z.Y. Yang Inorg. Chem. Commun. 12 8 2009 704 706
9. X.P. Yang, R.A. Jones, W.K. Wong, V. Lynch, M.M. Oye, and A.L. Holmes Chem. Commun. 7 2006 1836 1838
10. G. Chiericato Junior, A.P.S. Silva, and L.S. Guinesi Polyhedron 23 2004 1953 1960
11. M. Nath, and R. Yadov Bull. Chem. Soc. Jpn. 70 1997 1131
12. A.I. El-Said, A.S.A. Zidan, M.S. El-Meligy, A.A.M. Aly, and O.F. Mohammed Trans. Met. Chem. 26 2001 13
13. Z.M. Wang, H.K. Lin, S.R. Zhu, T.F. Liu, and Y.T. Chen J. Inorg. Biochem. 89 2002 97 106
14. M.Z. Wang, Z.X. Meng, B.L. Liu, G.L. Cai, C.L. Zhang, and X.Y. Wang Inorg. Chem. Commun. 8 4 2005 368 371
15. L. Canali, and D.C. Sherrington Chem. Soc. Rev. 28 1999 85 93
16. A.T. Chaviara, E.E. Kioseoglou, A.A. Pantazaki, A.C. Tsipis, P.A. Karipidis, D.A. Kyriakidis, and C.A. Bolos J. Inorg. Biochem. 102 2008 1749 1764
17. N. Mahalakshmi, and R. Rajavel Inter. J. Pharm. Technol. 2 4 2010 1133 1157
18. D. Sabolová, M. Kožurková, T. Plichta, Z. Ondrušová, D. Hudecová, M. Simkovič, H. Paulíková, and A. Valent Inter. J. Bio. Macromol. 48 2011 319 325
19. J. Cheng, Q. Lin, R. Hu, W. Zhu, H. Li, and D. Wang Cent. Eur. J. Chem. 7 1 2009 105 110
20. M.S.A. Begum, S. Saha, M. Nethaji, and A.R. Chakravarty J. Inorg. Biochem. 104 2010 477 484
21. D. Jianfanga, L. Lianzhi, L. Linweia, X. Taoa, and W. Daqia Chin. J. Chem. 29 2011 259 266
22. Laila H. Abdel-Rahman, Rafat M. El-Khatib, Lobna A.E. Nassr, Ahmed M. Abu-Dief, and Fakhr El-Din Lashin Spectrochim. Acta Part A: Mol. Biomol. Spectrosc. 111 2013 266 276
23. Laila H. Abdel-Rahman, Rafat M. El-Khatib, Lobna A.E. Nassr, and Ahmed M. Abu-Dief J. Mole. Struct. 1040 2013 9 18
24. A.K. Patra, T. Bhowmick, S. Roy, S. Ramakumar, and A.R. Chakravarty Inorg. Chem. 48 2009 2932 2943
25. R. Bonnett Chemical Aspects of Photodynamic Therapy 2000 Gordon and Breach London, UK
26. B.W. Henderson, T.M. Busch, L.A. Vaughan, N.P. Frawley, D. Babich, T.A. Sosa, J.D. Zollo, A.S. Dee, M.T. Cooper, D.A. Bellnier, W.R. Greco, and A.R. Oseroff Cancer Res. 60 2000 525 529
27. I. Şakiyan, E. Logoglu, S. Arslan, N. Sari, and N. Sakiyan Biometals 17 2004 115 120
28. A.M. Shaker, A.M. Awad, and L.A.E. Nassr Synth. React. Inorg. Metal - Org. Chem. 33 1 2003 103 107
29. H.T.S. Britton Hydrogen Ions fourth ed. 1952 Chapman and Hall London, UK
30. P.J. Hay, and W.R. Wadt J. Chem. Phys. 82 1985 270 283
31. M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, et al. Gaussian 03, Revision of C.01. Wallingford CT: Gaussian Inc.; 2004.
32. J. Murmur J. Mol. Biol. 3 1961 208 218
33. N. Raman, K. Pothiraj, and T. Baskaran J. Mol. Struct. 1000 2011 135 144
34. A. Wolf, G.H. Shimer, and T. Meehan Biochemistry 26 1987 6392 6396
35. S. Satyanarayana, J.C. Dabroniak, and J.B. Chaires Biochemistry 31 1992 9319 9324
36. M. Vujcic, S. Tufegdzic, Z. Vujcic, M.J. Gašic, and D. Sladic J. Serb. Chem. Soc. 72 2007 1265 1269
37. N. Raman, A. Kulandaisamy, and K. Jeyasubramanian Synth. React. Inor. Met. Org. Chem. 31 7 2001 1249 1260
38. S. Gopalakrishnan, R. Rajameena, and E. Vadivel Int. J. Pharmaceut. Sci. Drug Res. 4 1 2012 31 34
39. G. Kumar, S. Devi, R. Johari, and D. Kumar Eur. J. Med. Chem. 52 2012 269 274
40. E. Canpolat, and M. Kaya J. Coord. Chem. 55 2002 961 968
41. A.S. El-Tabl, F.A. EL-Saied, and A.N. Al-Hakimi J. Coord. Chem. 61 15 2008 2380 2401
42. N. Raman, J.D. Raja, and A. Sakthivel J. Chem. Sci. 119 4 2007 303 310
43. P.K. Sharma, and S.N. Dubey Proc. Ind. Acad. Sci. (Chem. Sci.) 6 1 1994 23 27
44. M.S.A. Begum, S. Saha, M. Nethaji, and A.R. Chakravarty J. Inorg. Bio. Chem. 104 2010 477 484
45. M. Thankamony, and K. Mo anan Ind. J. Chem. A46 2007 249
46. R. Garg, N. Fahmi, and R.V. Singh Russ. J. Coord. Chem. 34 2008 198 203
47. K. Nakamoto Infrared and Raman spectra of coordination compounds 1978 John Wiley New York pp. 143-253
48. P. Teyssie, and J.J. Charette Spectrochim. Acta 19 9 1963 1407 1423
49. A.M. Abdel-Mawgoud Synth. Inorg. Met. Org. Chem. 28 4 1998 555 570
50. G. Ibrahim, E. Chebli, M.A. Khan, and G.M. Bouet Transit. Met. Chem. 24 3 1999 294 298
51. M. Thomas, M.K.M. Nair, and R.K. Radhakrishan Synth React. Inorg. Met. Org. Chem. 25 1995 471 479
52. F. Ahmad, M. Parvez, S. Ali, M. Mazhar, and A. Munir Synth. React. Inorg. Met. Org. Chem. 32 4 2002 665 687
53. D.X. West, and A.A. Nasar Transit. Met. Chem. 24 1999 617 621
54. A.B.P. Lever Inorganic Electronic Spectroscopy 1968 Elsevier Publishing Amsterdam 326
55. J.H. Yoe, and A.L. Jones Ind. Eng. Chem. Anal. Ed. 16 1944 111 115
56. R. El-Shiekh, M. Akl, A. Gouda, and W. Ali J. Am. Sci. 7 4 2011 797 807
57. S.S. Shah, and R.G. Parmar Der. Pharm. Chem. 3 1 2011 318 321
58. P. Job Ann. Chem. 9 1928 113 203
59. R.M. Issa, A.A. Hassanein, I.M. El-Mehasseb, and R.I. Abed El-Wadoud Spectrochim. Acta A 65 2006 206 214
60. K.D. Sen, and D.M.P. Mingos Structure and Bonding: Chemical Hardness 80 1993 Springer Berlin
61. R.G. Parr, and W. Yang Density Functional Theory of Atoms and Molecules 1989 Oxford University Press Oxford
62. P. Geerlings, F. de Proft, and W. Langenaeker Chem. Rev. 103 2003 1793
63. P.K. Chattaraj, and B. Maiti J. Am. Chem. Soc. 125 2003 2705
64. R.G. Pearson Acc. Chem. Res. 26 1993 250
65. R.G. Pearson Chemical Hardness: Application From Molecules to Solid 1997 Wiley-VCH Weinheim
66. A. Vektariene, G. Vektaris, and J. Svoboda Arkivoc 7 2009 311
67. J.M. Kelly, A.B. Tossi, D.J. McConnell, and C.O. Uigin Nucl. Acids Res. 13 1985 6017 6034
68. A.M. Pyle, J.P. Rehmann, R. Meshoyrer, C.V. Kumar, N.J. Turro, and J.K. Barton J. Am. Chem. Soc. 111 1989 3051 3058
69. X.W. Liu, J. Li, H. Li, K.C. Zheng, H. Chao, and L.N. Ji J. Inorg. Biochem. 99 2005 2372 2380
70. B.C. Baguley, and M. LeBret Biochemistry 23 1984 937 943
71. Y. Liu, W. Mei, J. Lu, H. Zhao, L. He, and F. Wu J. Coord. Chem. 61 2008 3213 3224
72. R.B. Dixit, T.S. Patel, S.F. Vanparia, A.P. Kunjadiya, H.R. Keharia, and B.C. Dlxit Sci. Pharm. 79 2011 293 308
73. A. Hartwig Chem. - Biol. Interact. 184 2010 269 272
74. S. Shi, J. Liu, J. Li, K.C. Zheng, X.M. Huang, C.P. Tan, L.M. Chen, and L.N. Ji J. Inorg. Biochem. 100 2006 385 395
75. N. Nishat, S. Hasnain, and S.D. Asma J. Coord. Chem. 63 21 2010 3859 3870
76. P.G. Avajia, C.H.V. Kumar, S.A. Patilc, K.N. Shivanandad, and C. Nagaraju Eur J. Med. Chem. 44 9 2009 3552 3559
77. Z.H. Chohan, C.T. Supuran, and A. Scozzafava J. Enz. Inhib. Med. Chem. 19 2004 79 84
78. S.U. Rehman, Z.H. Chohan, F. Naz, and C.T. Supuran J. Enzy. Inhib. Med. Chem. 20 2005 333 340
79. Z.H. Chohan, M. Arif, Z. Shafiq, M. Yaqub, and C.T. Supuran J. Enz. Inhib. Med. Chem. 21 2006 95 103