Abstract
Two series of urea and thiourea derivatives (1a11a, 1b11b) have been synthesized; all the 22 compounds were reported for the first time. Their anti-proliferative activities against the melanoma cell line B16-F10 were evaluated. Among the compounds tested, compound 6b exhibited the most potent activity in melanoma cells growth inhibition (IC500.33 μM). The bioassay tests showed that anti-proliferative activities of these novel compounds were possibly caused by inhibition of ERK1/2 phosphorylation level. Therefore, compound 6b can be a potential anti-melanoma agent and an inhibitor of ERK1/2 phosphorylation deserving further research. © 2012 Informa UK, Ltd.
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Li, Q. S., Lv, P. C., Li, H. Q., Lu, X., Li, Z. L., Ruan, B. F., & Zhu, H. L. (2012). Synthesis and biological evaluation of novel N, N′-disubstituted urea and thiourea derivatives as potential anti-melanoma agents. Journal of Enzyme Inhibition and Medicinal Chemistry, 27(5), 708–714. https://doi.org/10.3109/14756366.2011.608665
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