Design, synthesis and cytotoxic activities of novel hybrid compounds between dihydrobenzofuran and imidazole
作者:Wen Chen、Xiao-Dong Yang、Yan Li、Li-Juan Yang、Xue-Quan Wang、Gao-Lan Zhang、Hong-Bin Zhang
DOI:10.1039/c1ob05116d
日期:——
A series of novel hybrid compounds between dihydrobenzofuran and imidazole has been prepared and evaluated in vitro against a panel of human tumor cell lines. The results suggest that substitution of the imidazolyl-1-position with an electron-donating dihydrobenzofuran, and the imidazolyl-3-position with a naphthylacyl or electron-rich phenacyl group, were vital for modulating cytotoxic activity.
我们制备了一系列新型二氢苯并呋喃与咪唑杂化化合物,并对一系列人类肿瘤细胞系进行了体外评估。结果表明,咪唑-1-位被电子供体二氢苯并呋喃取代,咪唑-3-位被萘酰基或富含电子的苯酰基取代,这对调节细胞毒性活性至关重要。