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Synthesis and antitumor activity evaluation of some novel pyrazolotriazine derivatives

Version 2 2017-01-19, 16:35
Version 1 2016-11-28, 17:02
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posted on 2017-01-19, 16:35 authored by Saad R. Atta-Allah, Rasha S. Gouhar, Magdy M. Hemdan, Wael S. I. Abou-Elmagd, David S. A. Haneen, Kamal A. A. Kandeel, Ahmed S. A. Youssef

6-Aminopyrazolo[1,2-a][1,2,4]triazine-4,8-dione derivative 3 was obtained upon the reaction of the acid hydrazide derivative 2a with ethyl cyanoacetate. The reactions of 3 with several electrophiles such as aldehydes, isatin, acetic anhydride, phenyl isocyanate, benzoyl isothiocyanate, and p-toluenesulfonyl chloride were studied. The structures of the newly synthesized compounds were established on the basis of IR, 1H NMR, mass spectra, and elemental analyses. The antitumor activities of some selective compounds were examined against two cell lines as liver carcinoma cell line (HEPG-2) and human breast cancer cell line (MCF7).

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