In vitro anticancer and antibacterial activities of octahedral ruthenium(III) complexes with hydroxamic acids. Synthesis and spectroscopic characterization
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  • 作者:Raj Kaushal ; Sheetal
  • 关键词:Ruthenium complexes ; hydroxamic acids ; antibacterial and anticancer activity
  • 刊名:Russian Journal of General Chemistry
  • 出版年:2016
  • 出版时间:February 2016
  • 年:2016
  • 卷:86
  • 期:2
  • 页码:360-367
  • 全文大小:248 KB
  • 参考文献:1.Gowri, S., Muthukumar, M., Krishnaraj, S., Viswanathamurthi, P., Prabhakaran, R., and. Natarajan, K., J. Coord. Chem., 2010, vol. 63, p. 524. DOI: 10.1080/00958970903499651.CrossRef
    2.Gasser, G. and Nolte, N.M., Curr. Opin. Chem. Biol., 2012, vol. 16, p. 84. DOI: 10.1016/j.cbpa.2012.01.013.CrossRef
    3.Khan, N., Farina, Y., Mun, L.K., Rajab, N.F., and Awang, N., J. Organomet. Chem., 2014, vols. 763–764, p. 26. DOI: 10.1016/j.jorganchem.2014.04.015.CrossRef
    4.Kaushal, R. and Thakur, S., Chem. Eng. Trans., 2013, vol. 32, p. 1974. DOI: 10.3303/CET1332301.
    5.Filak, L.K., Goschl, S., Heffeter, P., Samper, K.G., Egger, A.E., Jakupec, M.A., Keppler, B.K., Berger, W., and Arion, V.B., Organometallics, 2013, vol. 32, p. 903. DOI: 10.1021/om3012272.CrossRef
    6.Hearn, J.M., Canelon, I.R., Qamar, B., Liu, Z., Portman, I.H., and Sadler, P.J., ACS Chem. Biol., 2013, vol. 8, p. 1335. DOI: 10.1021/cb400070a.CrossRef
    7.Kaushal, R., Kumar, N., Chaudhary, A., Arora, S., and Awasthi, P., Bioinorg. Chem. Appl., 2014, p. 1. DOI: 10.1155/2014/142828
    8.Rani, S., Kumar, S., and Chandra, S., Spectrochim. Acta, Part A, 2014, vol. 118, p. 244. DOI: 10.1016/j.saa.2013.08.079.CrossRef
    9.Butler, J.S. and Sadler, P.J., Curr. Opin. Chem. Biol., 2013, vol. 17, p. 175. DOI: 10.1016/j.cbpa.2013.01.004.CrossRef
    10.Reedijk, J., Platinum Met. Rev., 2008, vol. 52, p. 2. DOI: 10.1595/147106708X255987.CrossRef
    11.Pena, B., David, A., Pavani, C., Baptista, M.S., Pellois, J.P., Turro, C., and Dunbar, K.R., Organometallics, 2014, vol. 33, p. 1100. DOI: 10.1021/om500001h.CrossRef
    12.Clarke, M.J., Coord. Chem. Rev., 2003, vol. 236, p. 209. DOI: 10.1016/S0010-8545(02)00312-0.CrossRef
    13.Ronconi, L. and Sadler, P.J., Coord. Chem. Rev., 2007, vol. 251, p. 1633. DOI: 10.1016/j.ccr.2006.11.017.CrossRef
    14.Rademaker-Lakhai, J.M., Van den Bongard, D., Pluim, D., Beijnen, J.H., and Schellens, J.H., Clin. Cancer Res., 2004, vol. 10, p. 3717. DOI: 10.1158/1078-0432.CCR-03-0746.CrossRef
    15.Wang, Y., Miao, X., Liu, Y., Li, F., Liu, Q., Sun, J., and Cai, L., Oxid. Med. Cell. Longevity, 2014, vol. 2014, p. 1. DOI: 10.1155/2014/641979.
    16.Elek, H., Smart, L., Martin, J., Ahmad, S., Weeks, R.G., Welham, S., Nadasy, M., Pickett, J.A., and Werner, C.P., Ann. Appl. Biol., 2013, vol. 162, p. 100.CrossRef
    17.Rodrigues, G.C., Feijo, D.F., Bozza, M.T., Pan, P., Vullo, D., Parkkila, S., Supuran, C.T., Capasso, C., Aguiar, A.P., and Vermelho, A.B., J. Med. Chem., 2014, vol. 57, p. 298. DOI: 10.1021/jm400902y.CrossRef
    18.Tolosa, S., Diez, N.M., Hidalgo, A., and Sanson, J.A., RSC Adv., 2014, vol. 4, p. 44757. DOI: 10.1039/ C4RA06124A.CrossRef
    19.Cheng, C., Wang, J., Yang, X., Li, A. and Philippe, C., J. Hazard. Mater., 2014, vol. 264, p. 332.CrossRef
    20.Lopez, Y.S., Vidal, J.A.G., and Basurto, J.C., Appl. Biochem. Biotechnol., 2014, vol. 173, p. 1907.CrossRef
    21.Brown, D.A., Googan, R.A., Fitzpatrick, N.J., Glass, W.K., Abukshima, D.E., Shiels, L., Ahlgran, M., Smolander, K., Pakkanen, T.T., Pakkanen, T.A., and Perakyla, M., J. Chem. Soc., Perkin Trans. 2, 1996, p. 2673. DOI: 10.1039/P29960002673.
    22.Dobosz, A., Dudarenko, N.M., Fritsky, I.O., Glowiak, T., Karaczyn, A., Kozlowski, H., Sliva, T.Y., and Swiatek-Kozlowska, J., J. Chem. Soc., Dalton Trans., 1999, p. 743.
    23.Farkas, E., Enyedy, E.A., Micera, G., and Garribba, E., Polyhedron, 2000, vol. 19, p. 1727.CrossRef
    24.Sharma, N., Kumari, M., Kumar, V., and Chaudhry, S.C., J. Enzyme Inhib. Med. Chem., 2010, vol. 25, p. 708. DOI: 10.3109/14756360903540292CrossRef
    25.Shang, X., Cui, J., Wu, J., Pombeiro, A.J.L., and Li, Q., J. Inorg. Biochem., 2008, vol. 102, p. 901.CrossRef
    26.Yousef, T.A., El-Reash, G.M.A., El-Gammal, O.A., and Bedier, R.A., J. Mol. Struct., 2013, vol. 1035, p. 307. DOI: 10.1016/j.molstruc.2012.10.058.CrossRef
    27.Sharma, V.K. and Srivastava, S., Turk. J. Chem., 2006, vol. 30, p. 755.
    28.Ferrari, M., Fornasiero, M.C., and Isetta, A.M., J. Immunol. Methods, 1990, vol. 131, p. 165. DOI: 10.1016/0022-1759(90)90187-Z.CrossRef
    29.Parekh, J., Inamdhar, P., Nair, R., Baluja, S., and Chanda, S., J. Serb. Chem. Soc., 2005, vol. 70, p. 1155. DOI: 10.2298/JSC0510155P.CrossRef
  • 作者单位:Raj Kaushal (1)
    Sheetal (1)

    1. Department of Chemistry, National Institute of Technology, Hamirpur, Himachal Pradesh, 177005, India
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Chemistry
    Russian Library of Science
  • 出版者:MAIK Nauka/Interperiodica distributed exclusively by Springer Science+Business Media LLC.
  • ISSN:1608-3350
文摘
Five new ruthenium(III) complexes of the general formulas [RuCl(H2O)L2] (1–4) and [RuCl3(H2O)(HL)2] (5), where L = benzohydroximato (1), salicylhydroximato (2), acetohydroximato (3), hydroxyureato (4), LH = N-hydroxy-N-phenylbenzamide (5), were synthesized by reaction of RuCl3 · 3H2O with the corresponding hydroxamic acids at a molar ratio of 1: 2 molar. The complexes were characterized by elemental analyses and FT-IR, UV-Vis, 1H and 13C NMR, and mass spectra. The complexes showed higher antibacterial activity against ten pathogenic bacterial strains than the corresponding ligands. The anticancer activity of the complexes against IMR-32 (neuroblastoma) cancer and CHO (Chinese hamster ovary) normal cell lines was evaluated using MTT assay with respect to camptothecin as control. Complex 5 was found to exhibit an appreciable cytotoxicity against IMR-32 cell line with an IC50 value of 102.27 μM.

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