Synthesis, Crystal Structure and Evaluation of Cancer Inhibitory Activity of 4-[indol-3-yl-Methylene]-1<i>H</i>-pyrazol-5(4<i>H</i>)-one derivatives
作者:Lingling Jing、Liang Wang、Yinglan Zhao、Rui Tan、Xiumei Xing、Ting Liu、Wencai Huang、Youfu Luo、Zicheng Li
DOI:10.3184/174751912x13501278349974
日期:2012.12
series of 4-(1H-indol-3-yl-methylene)-1H-pyrazol-5(4H)-one derivatives have been synthesised. The Z structure of 4-[(1-methyl-1H-indol-3-yl)methylene]-3-phenyl-1-p-tolyl-1H-pyrazol-5-one was determined by X-ray crystallography. The antitumour activity was evaluated against five cancer cells by MTT assay. [(1H-Indol-3-yl)methylene]-1-(2,4-dini-trophenyl)-3-methyl-1H-pyrazole-5-one and 4-4-[(1-benzy
已经合成了一系列 4-(1H-indol-3-yl-methylene)-1H-pyrazol-5(4H)-one 衍生物。4-[(1-methyl-1H-indol-3-yl)methylene]-3-phenyl-1-p-tolyl-1H-pyrazol-5-one 的 Z 结构由 X 射线晶体学确定。通过 MTT 测定评估了对五种癌细胞的抗肿瘤活性。[(1H-Indol-3-yl)methylene]-1-(2,4-dini-trophenyl)-3-methyl-1H-pyrazole-5-one 和 4-4-[(1-benzyl-1H- indol-3-yl)methylene]-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl}-benzoic acid 对测试癌细胞具有与 5-UF 相似的抗癌活性(除了A375)。几乎所有的目标化合物都对