Dehydrozingerone based 1-acetyl-5-aryl-4,5-dihydro-1H-pyrazoles: Synthesis, characterization and anticancer activity
作者:Zoran Ratković、Jovana Muškinja、Adrijana Burmudžija、Branislav Ranković、Marijana Kosanić、Goran A. Bogdanović、Bojana Simović Marković、Aleksandar Nikolić、Nebojša Arsenijević、Snežana Đorđevic、Rastko D. Vukićević
DOI:10.1016/j.molstruc.2015.12.079
日期:2016.4
4-alkoxy-3-methoxyphenyl) was prepared, starting from 4-(4-hydroxy-3-methoxyphenyl)-3-buten-2-one, dehydrozingerone, and its alkyl derivatives. Their in vitro cytotoxic activity against some cancer cell lines was tested, showing significant anticancer activity. All the new compounds were well characterized by IR, 1H, 13C NMR and ESI-MS spectroscopy and physical data, whereas structures of two of them were determined
摘要 以 4-(4) 为原料制备了小系列的 1-乙酰基-5-芳基-4,5-二氢-1H-吡唑(芳基 = 4-羟基-3-甲氧基苯基和 4-烷氧基-3-甲氧基苯基)。 -羟基-3-甲氧基苯基)-3-丁烯-2-酮、脱氢姜油酮及其烷基衍生物。测试了它们对一些癌细胞系的体外细胞毒活性,显示出显着的抗癌活性。所有新化合物均通过 IR、1H、13C NMR 和 ESI-MS 光谱和物理数据进行了很好的表征,而其中两种化合物的结构由单晶 X 射线分析确定。