Synthesis of new pyrazole, triazole, and thiazolidine-pyrimido [4, 5-b] quinoline derivatives with potential antitumor activity-Reference-Cited by-同舟云学术

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Synthesis of new pyrazole, triazole, and thiazolidine-pyrimido [4, 5-b] quinoline derivatives with potential antitumor activity

Published:2012-03 Issue:3 Volume:35 Page:437-445
ISSN:0253-6269
Container-title:Archives of Pharmacal Research
language:en
Short-container-title:Arch. Pharm. Res.

Author:

Abu-Hashem Ameen Ali,Aly Ahmed S.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12272-012-0306-5.pdf

Reference18 articles.

1. Abu-Hashem, A. A., El-Shehry, M. F., and Badria, F. A., Design and synthesis of novel thiophene carbohydrazide, thienopyrazole and thienopyrimidine derivatives as antioxidant and antitumor agents. Acta Pharm., 60, 311–323 (2010).

2. Abu-Hashem, A. A., Youssef, M. M., and Hussein, H. A. R., Synthesis, antioxidant, antitumor activities of some new thiazolopyrimidines, pyrrolothiazolopyrimidines and triazolopyrrolothiazolopyrimidines derivatives. J. Chin. Chem. Soc., 58, 1–8 (2011).

3. Ali, H. I., Tomita, K., Akaho, E., Kambara, H., Miura, S., Hayakawa, H., Ashida, N., Kawashima, Y., Yamagishi, T., Ikeya, H., Yoneda, F., and Nagamatsu, T., Antitumor studies. Part 1: Design, synthesis, antitumor activity, and AutoDock study of 2-deoxo-2-phenyl-5-deazaflavins and 2-deoxo-2-phenylflavin-5-oxides as a new class of antitumor agents. Bioorg. Med. Chem., 15, 242–256 (2007).

4. Ali, H. I., Ashidab, N., and Nagamatsu, T., Antitumor studies. Part 4: Design, synthesis, antitumor activity, and molecular docking study of novel 2-substituted 2-deoxoflavin-5-oxides, 2-deoxoalloxazine-5-oxides, and their 5-deaza analogs. Bioorg. Med. Chem., 16, 922–940 (2008a).

5. Ali, H. I., Tomita, K., Akaho, E., Kunishima, M., Kawashima, Y., Yamagishi, T., Ikeya, H., and Nagamatsu, T., Antitumor studies e Part 2: Structureeactivity relationship study for flavin analogs including investigations on their in vitro antitumor assay and docking simulation into protein tyrosine kinase. Eur. J. Med. Chem., 43, 1376–1389 (2008b).

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