Abstract
The chalcone basic skeleton is a unique template which is associated with widespread biological activities. In the present study, a series of novel bichalcones linked with a 1,4-dimethylenepiperazine moiety was prepared through Mannich reaction and Clasien-Schmidt condensation. The synthetic analogs 2-16 were subjected into the cytotoxicity examinations using a panel of 25 human tumor cell lines. Among the tested compounds, 3 and 4 which possessed the 3-pyridyl and phenyl groups as the substructure, respectively, displayed significant cytotoxicity against all the tumor cell lines. The results suggested that these bichalcones were potential to be the anti-cancer lead drugs. © 2011 Pharmaceutical Society of Japan.
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Reddy, M. V. B., Chen, S. S., Lin, M. L., Chan, H. H., Kuo, P. C., & Wu, T. S. (2011). Preparation of a series of novel bichalcones linked with a 1,4- dimethylenepiperazine moiety and examination of their cytotoxicity. Chemical and Pharmaceutical Bulletin, 59(12), 1549–1554. https://doi.org/10.1248/cpb.59.1549
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