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Synthesis and biological evaluation of novel N, N′-disubstituted urea and thiourea derivatives as potential anti-melanoma agents

机译:新型N,N′-二取代尿素和硫脲衍生物作为潜在抗黑素瘤药物的合成及生物学评价

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摘要

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.
机译:合成了两个系列的脲和硫脲衍生物(1a11a,1b11b);所有22种化合物都是首次报道。评估了它们对黑素瘤细胞系B16-F10的抗增殖活性。在测试的化合物中,化合物6b在抑制黑素瘤细胞生长方面表现出最有效的活性(IC500.33μM)。生物测定测试表明,这些新化合物的抗增殖活性可能是由于抑制ERK1 / 2磷酸化水平引起的。因此,化合物6b可能是潜在的抗黑色素瘤药物和ERK1 / 2磷酸化抑制剂,值得进一步研究。

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