Synthesis and inhibitory activity of new benzimidazole derivatives against Burkitt's lymphoma promotion.

Bioorg Med Chem

Chemistry of Natural and Microbial Products Department, National Research Center, Dokki, Cairo, Egypt.

Published: October 2007

AI Article Synopsis

  • * The newly created compounds were tested for their ability to inhibit the activation of the Epstein-Barr virus-early antigen (EBV-EA) triggered by a specific chemical (TPA).
  • * Among the tested compounds, 6d showed significant inhibitory activity, while 5a and 6e also demonstrated effectiveness.

Article Abstract

As a continuation to our previous work concerning antitumor benzimidazoles, we have synthesized series of new derivatives of 2-(1-benzyl-2-methyl-1H-benzimidazol-5-ylimino)-3-(substituted)-thiazolidin-4-one (6a-e), 3-(2-methyl-1H-benzimidazol-5-yl)-2-substituted-thiazolidin-4-one (9a-f) and we have studied their inhibitory activity against the Epstein-Barr virus-early antigen (EBV-EA) activation introduced by 12-O-tetradecanoylphorbol-13-acetate (TPA). Compound 6d was found to be significantly active and compounds 5a and 6e were also active.

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Source
http://dx.doi.org/10.1016/j.bmc.2007.04.010DOI Listing

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