The reaction of cyanoacetylhydrazine with ω-bromo(4-methyl) acetophenone: Synthesis of heterocyclic derivatives with antitumor activity

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Abstract

New approaches for the synthesis of hydrazide-hydrazone derivatives were demonstrated as well as some heterocyclizations of such derivatives to afford 1,3,4-triazine, pyridine and 1,3,4-oxadiazine derivatives. The antitumor evaluation of the newly synthesized products against three cancer cell lines, namely breast adenocarcinoma (MCF-7), non-small cell lung cancer (NCI-H460) and CNS cancer (SF-268) were recorded. Most of the synthesized compounds showed high inhibitory effects. © 2010 by the authors.

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Mohareb, R. M., & Mohamed, A. A. (2010). The reaction of cyanoacetylhydrazine with ω-bromo(4-methyl) acetophenone: Synthesis of heterocyclic derivatives with antitumor activity. Molecules, 15(5), 3602–3617. https://doi.org/10.3390/molecules15053602

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