Synthesis and Cytotoxic Activity of Salicyloyl Hydrazone Derivatives

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Abstract:

Three salicyloyl hydrazone derivatives (compounds 1-3) were prepared by reacting salicyloyl hydrazine with substituted formaldehydes. Their structures were characterized by melting point, 1H-NMR, ESI-MS and elemental analyses. The cytotoxic activity of compounds 1-3 was evaluated in vitro against Hela cells (human cervical cancer cells). The results revealed that all the compounds showed cytotoxic activity, with IC50 values lower than 15 μM.

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522-525

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May 2013

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© 2013 Trans Tech Publications Ltd. All Rights Reserved

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[1] T.R. Frieden, T.R. Sterling, S.S. Munsiff, C.J. Watt, C. Dye: Lancet Vol. 362 (2003), p.887

DOI: 10.1016/s0140-6736(03)14333-4

Google Scholar

[2] B.R. Bloom, C.J.L. Murray: Science 257 (1992), p.1055

Google Scholar

[3] World Health Organization report on TB epidemic, Global TB programme, World Health Organization, Geneva, (1997)

Google Scholar

[4] M.T. Cocco, C. Congiu, V. Onnis, M.C. Pusceddu, M.L. Schivo, A.D. Logu: Eur. J. Med. Chem. Vol. 34 (1999), p.1071

DOI: 10.1016/s0223-5234(99)00124-5

Google Scholar

[5] D. Sriram, P.Yogeeswari, K.Madhu: Bioorg. Med. Chem. Lett. Vol. 15 (2006), p.4502

Google Scholar

[6] C. Loncle, J.M. Brunel, N. Vidal, M. Dherbomez, Y. Letourneux: Eur. J. Med. Chem., Vol. 39 (2004), 1067

Google Scholar

[7] S.K. Sridhar, S.N. Pandeya, J.P. Stables, R. Atmakuru: Eur. J. Pharm. Sci. Vol. 16 (2002), p.129

Google Scholar

[8] A.R. Todeschini, A.L.P. Miranda, K.C.M. Silva, S.C. Parrini, E.J. Barreiro: Eur. J. Med. Chem. Vol. 33 (1998), p.189

Google Scholar

[9] P. Melnyk, V. Leroux, C. Sergheraert, P. Grellier: Bioorg. Med. Chem. Lett. Vol. 16 (2006), p.31

Google Scholar

[10] D.G. Rando, D.N. Sato, L. Siqueira, A. Malvezzi, C.Q.F. Leite, A.T. Amaral, E.I. Ferreira, L.C. Tavares: Bioorg. Med. Chem. Vol. 10 (2002), p.557

Google Scholar

[11] J. Patole, U. Sandbhor, S. Padhye, D.N. Deobagkar, C.E. Anson, A. Powell: Bioorg. Med. Chem. Lett. Vol. 13 (2003), p.51

Google Scholar

[12] R. Maccari, R. Ottana, M.G. Vigorita: Bioorg. Med. Chem. Lett. Vol. 15, (2005), p.2509

Google Scholar

[13] N. Georgieva, V. Gadjeva: Biochemistry-moscow+ Vol. 67 (2002), p.705

Google Scholar

[14] X. Chen, C. Plasencia, Y. Hou, N. Neamati: J. Med. Chem. Vol. 48 (2005), p.1098.

Google Scholar