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.
Similar content being viewed by others
References
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
Monsen, E.R., J. Am. Diet. Assoc., 2000, vol. 100, p. 637. doi https://doi.org/10.1016/S0002-8223(00)00189-9
May, S.W., Exp. Opin. Invest. Drugs, 1999, vol. 8, p. 1017. doi https://doi.org/10.1517/13543784.8.7.1017
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
Hocman, G., Int. J. Biochem., 1988, vol. 20, p. 123. doi https://doi.org/10.1016/0020-711X(88)90475-2
Jariwalla, R.J., Gangapurkar, B. and Nakamura, D., Br. J. Nutr., 2009, vol. 101, p. 182. doi https://doi.org/10.1017/S0007114508998305
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
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
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
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
El-Bayoumy, K., Mutat. Res., 2001, vol. 475, p. 123. doi https://doi.org/10.1016/S0027-5107(01)00075-6
Šibor, J. and Pazdera, P., Molecules, 1996, vol. 1, p. 157. doi https://doi.org/10.1007/s007830050031
Abdel-Hafez, S.H., Russ. J. Org. Chem., 2005, vol. 41, p. 396. doi https://doi.org/10.1007/s11178-005-0177-z
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
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
Gewald, K., Jeschke, T., and Gruner, M., J. Prakt. Chem., 1991, vol. 333, p. 229. doi https://doi.org/10.1002/prac.19913330204
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
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.
Boyd, M.R., and Paull, K.D., Drug Dev. Res., 1995, vol. 34, p. 91. doi https://doi.org/10.1002/ddr.430340203
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
Author information
Authors and Affiliations
Corresponding author
Additional information
Conflict of Interest
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.
Rights and permissions
About this article
Cite this article
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
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070428019080189