Elserwy, W., Mohamed, N., Kassem, E., Mahmoud, K., Mounier, M. (2016). Synthesis, Biological Evaluation and Docking Analysis of Some Novel Quinazolin Derivatives as Antitumor Agents. Iranian Journal of Pharmaceutical Research, 15(1), 179-196. doi: 10.22037/ijpr.2016.1799
Walaa salah Elserwy; Neama A Mohamed; Emad M. M. Kassem; Khaled Mahmoud; M. M Mounier. "Synthesis, Biological Evaluation and Docking Analysis of Some Novel Quinazolin Derivatives as Antitumor Agents". Iranian Journal of Pharmaceutical Research, 15, 1, 2016, 179-196. doi: 10.22037/ijpr.2016.1799
Elserwy, W., Mohamed, N., Kassem, E., Mahmoud, K., Mounier, M. (2016). 'Synthesis, Biological Evaluation and Docking Analysis of Some Novel Quinazolin Derivatives as Antitumor Agents', Iranian Journal of Pharmaceutical Research, 15(1), pp. 179-196. doi: 10.22037/ijpr.2016.1799
Elserwy, W., Mohamed, N., Kassem, E., Mahmoud, K., Mounier, M. Synthesis, Biological Evaluation and Docking Analysis of Some Novel Quinazolin Derivatives as Antitumor Agents. Iranian Journal of Pharmaceutical Research, 2016; 15(1): 179-196. doi: 10.22037/ijpr.2016.1799
Synthesis, Biological Evaluation and Docking Analysis of Some Novel Quinazolin Derivatives as Antitumor Agents
Different acid chlorides (2a-d) reacted with anthranilic acid to produce 2-substituted-3, 1-benzoxazin-4-one (3a-d) which was used as starting material to synthesize some condensed and non-condensed heterocyclic compounds by reaction with nitrogen nucleophiles e.g., hydrazine hydrate, and formamide. Some of the newly synthesized analogues were chosen to evaluate their cytotoxic activity against human liver carcinoma cell lines (HePG2– MCF7– A549). The docking and the cytotoxic activity results revealed that nearly all of the compounds containing N-phenyl aniline showed significant inhibition for the three cell lines.
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