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Synthesis and Anticancer Activity of Certain Selenophene Derivatives

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Abstract

Selenopheno[2,3-d]pyrimidine- and selenopheno[2,3-d][1,2,3]triazine-containing compounds were synthesized starting from 2-amino-5,6,7,8-tetrahydro-4H-cyclohepta[b]selenophene-3-carbonitrile. In vitro anticancer activity of the newly synthesized compounds was tested using 60 different human cancer cell lines.

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References

  1. Heyland, D.K., Dhaliwal, R., Suchner, U., and Berger, M.M., Intensive Care Med., 2005, vol. 31, p. 327. doi https://doi.org/10.1007/s00134-004-2522-z

    Article  Google Scholar 

  2. Monsen, E.R., J. Am. Diet. Assoc., 2000, vol. 100, p. 637. doi https://doi.org/10.1016/S0002-8223(00)00189-9

    Article  CAS  Google Scholar 

  3. May, S.W., Exp. Opin. Invest. Drugs, 1999, vol. 8, p. 1017. doi https://doi.org/10.1517/13543784.8.7.1017

    Article  CAS  Google Scholar 

  4. Silva, V.D., Woznichak, M.M., Burns, K.L., Grant, K.B., and May, S.W., J. Am. Chem. Soc., 2004, vol. 126, p. 2409. doi https://doi.org/10.1021/ja037294j

    Article  Google Scholar 

  5. Hocman, G., Int. J. Biochem., 1988, vol. 20, p. 123. doi https://doi.org/10.1016/0020-711X(88)90475-2

    Article  CAS  Google Scholar 

  6. Jariwalla, R.J., Gangapurkar, B. and Nakamura, D., Br. J. Nutr., 2009, vol. 101, p. 182. doi https://doi.org/10.1017/S0007114508998305

    Article  CAS  Google Scholar 

  7. Franchetti, P., Cappellacci, L., Sheikha, G.A., Jayaram, H.N., Gurudutt, V.V., Sint, T., Schneider, B.P., Jones, W.D., Goldstein, B.M., Perra, G., Montis, A.D., Loi, A.G., Colla, P.L. and Grifantini, M., J. Med. Chem., 1997, vol. 40, p. 1731. doi https://doi.org/10.1021/jm960864o

    Article  CAS  Google Scholar 

  8. Juang, S.H., Lung, C.C., Hsu, P.C., Hsu, K.S., Li, Y.C., Hong, P.C., Shiah, H.S., Kuo, C.C., Huang, C.W., Wang, Y.C., Huang, L., Chen, T.S., Chen, S.F., Fu, K.C., Hsu, C.L., Lin, M.J., Chang, C.J., Ashendel, C.L., Chan, T.C.K., Chou, K.M. and Chang, J.Y., Mol. Cancer Ther., 2007, vol. 6, p. 193. doi https://doi.org/10.1158/1535-7163.MCT-06-0482

    Article  CAS  Google Scholar 

  9. Sanmartín, C., Plano, D., Domínguez, E., Font, M., Calvo, A., Prior, C., Encío, I. and Palop, J.A., Molecules, 2009, vol. 14, p. 3313. doi https://doi.org/10.3390/molecules14093313

    Article  Google Scholar 

  10. Plano, D., Moreno, E., Font, M., Encío, I., Palop, J. A. and Sanmartín, C., Arch. Pharm. Chem. Life Sci., 2010, vol. 10, p. 680. doi https://doi.org/10.1002/ardp.201000014

    Article  Google Scholar 

  11. El-Bayoumy, K., Mutat. Res., 2001, vol. 475, p. 123. doi https://doi.org/10.1016/S0027-5107(01)00075-6

    Article  CAS  Google Scholar 

  12. Šibor, J. and Pazdera, P., Molecules, 1996, vol. 1, p. 157. doi https://doi.org/10.1007/s007830050031

    Google Scholar 

  13. Abdel-Hafez, S.H., Russ. J. Org. Chem., 2005, vol. 41, p. 396. doi https://doi.org/10.1007/s11178-005-0177-z

    Article  CAS  Google Scholar 

  14. Seck, P., Thomae, D., Perspicace, E., Hesse, S., and Kirsch, G., Arkivoc, 2012, vol. 3, p. 431. doi https://doi.org/10.3998/ark.5550190.0013.329

    Google Scholar 

  15. Kotaiah, Y., Nagaraju, K., Harikrishna, N., Rao, C.V., Yamini, L., and Vijjulatha, M., Eur. J. Med. Chem., 2014, vol. 75, p. 195. doi https://doi.org/10.1016/j.ejmech.2014.01.006

    Article  CAS  Google Scholar 

  16. Gewald, K., Jeschke, T., and Gruner, M., J. Prakt. Chem., 1991, vol. 333, p. 229. doi https://doi.org/10.1002/prac.19913330204

    Article  CAS  Google Scholar 

  17. Kandeel, M.M., Mounir, A.A., Refaat, H.M. and Kassab, A.E., J. Chem. Res. 2012, vol. 36, p. 105. doi https://doi.org/10.3184/174751912X13282020691270

    Article  CAS  Google Scholar 

  18. Alley, M.C., Scudiere, D.A., Monks, A., Hursey, M.L., Czerwinski, M.J., Fine, D.L., Abbott, B.J., Mayo, J.G., Shoemaker, R.H., and Boyd, M.R., Cancer Res., 1988, vol. 48, p. 589.

    CAS  PubMed  Google Scholar 

  19. Boyd, M.R., and Paull, K.D., Drug Dev. Res., 1995, vol. 34, p. 91. doi https://doi.org/10.1002/ddr.430340203

    Article  CAS  Google Scholar 

  20. Grever, M.R., Schepartz, S.A., and Chabner, B.A., Semi. Oncol., 1992, vol. 19, p. 622. doi https://doi.org/10.5555/uri:pii:009377549290032V

    CAS  Google Scholar 

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Correspondence to M. E. Adly.

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The authors declare no conflict of interest.

Russian Text © The Author(s), 2019, published in Zhurnal Organicheskoi Khimii, 2019, Vol. 55, No. 8, pp. 1307.

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Adly, M.E., Gedawy, E.M., El-Malah, A.A. et al. Synthesis and Anticancer Activity of Certain Selenophene Derivatives. Russ J Org Chem 55, 1189–1196 (2019). https://doi.org/10.1134/S1070428019080189

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