Antitumor agents. Part 3: synthesis and cytotoxicity of new trans -Stilbene benzenesulfonamide derivatives
作者:Li-Ming Yang、Shwu-Jiuan Lin、Fen-Lin Hsu、Tsang-Hsiung Yang
DOI:10.1016/s0960-894x(02)00092-6
日期:2002.4
A new series of trans-stilbene benzenesulfonamide derivatives were designed and synthesized as potential antitumor agents. These new compounds were evaluated in the National Cancer Institute's 60 human tumor cell line in vitro screen. Compounds 9-13 were cytotoxic against several cell lines. Notably, two compounds, 9 and 12, demonstrated selective cytotoxic activity against BT-549 breast cancer (GI(50)=0
设计并合成了一系列新的反式二苯乙烯苯磺酰胺衍生物作为潜在的抗肿瘤药物。这些新化合物在美国国家癌症研究所的60种人类肿瘤细胞系体外筛选中进行了评估。化合物9-13对几种细胞系具有细胞毒性。值得注意的是,两种化合物9和12分别显示出对BT-549乳腺癌(GI(50)= 0.205 microM)和HT-29结肠癌(GI(50)= 0.554 microM)的选择性细胞毒活性。