Synthesis, anti-proliferative activity, theoretical and 1H NMR experimental studies of Morita–Baylis–Hillman adducts from isatin derivatives
作者:Vinicius B. M. Brito、Gilmar F. Santos、Thiago D. S. Silva、Júlia L. C. Souza、Gardenia C. G. Militão、Felipe T. Martins、Fábio P. L. Silva、Boaz G. Oliveira、Edigenia C. C. Araújo、Mário L. A. A. Vasconcellos、Claudio G. Lima-Júnior、Edilson B. Alencar-Filho
DOI:10.1007/s11030-019-09950-7
日期:2020.2
nucleus) can be used as interesting starting points to Morita–Baylis–Hillman adducts derivatives, a class of compounds with good cytotoxic potential. In this paper, we present the synthesis, anti-proliferative activity against lung cancer cell line and a theoretical conformational study of 21 of Morita–Baylis–Hillman adducts from isatin derivatives, by DFT quantum chemical calculations, followed by a
摘要季或螺环3-取代的-3-羟基-2-氧吲哚被认为是一种特权的支架。换句话说,它是存在于具有广泛生物活性的几种化合物上的分子核心。在其前体中,活化的酮(isatin核)可用作Morita-Baylis-Hillman加合物衍生物的有趣起点,Morita-Baylis-Hillman加合物衍生物是一类具有良好细胞毒性潜力的化合物。在本文中,我们通过DFT量子化学计算,然后通过SAR和QSAR分析,介绍了21种Isita衍生物的Morita-Baylis-Hillman加合物的合成,抗肺癌细胞的活性以及理论构象研究。此外,强调了一种有效的合成方案和良好的生物活性特征,有关1可提供1 H NMR实验光谱,分子建模结果和晶体学数据。 图形概要