Novel Capsaicin Analogues as Potential Anticancer Agents: Synthesis, Biological Evaluation, and<i>In Silico</i>Approach
作者:Mariana C. F. C. B. Damião、Kerly F. M. Pasqualoto、Adilson K. Ferreira、Sarah F. Teixeira、Ricardo A. Azevedo、José A. M. Barbuto、Fanny Palace-Berl、Gilberto C. Franchi-Junior、Alexandre E. Nowill、Maurício T. Tavares、Roberto Parise-Filho
DOI:10.1002/ardp.201400233
日期:2014.12
A novel class of benzo[d][1,3]dioxol‐5‐ylmethyl alkyl/aryl amide and ester analogues of capsaicin were designed, synthesized, and evaluated for their cytotoxic activity against human and murine cancer cell lines (B16F10, SK‐MEL‐28, NCI‐H1299, NCI‐H460, SK‐BR‐3, and MDA‐MB‐231) and human lung fibroblasts (MRC‐5). Three compounds (5f, 6c, and 6e) selectively inhibited the growth of aggressive cancer
设计、合成了一类新的苯并[d][1,3]二氧戊环-5-基甲基烷基/芳基酰胺和辣椒素的酯类似物,并评估了它们对人和鼠癌细胞系(B16F10,SK- MEL-28、NCI-H1299、NCI-H460、SK-BR-3 和 MDA-MB-231) 和人肺成纤维细胞 (MRC-5)。三种化合物(5f、6c 和 6e)在微摩尔 (µM) 范围内选择性抑制侵袭性癌细胞的生长。此外,探索性数据分析指出拓扑和电子分子特性是负责对一组研究化合物进行区分的过程。研究结果表明,应用设计策略,除了提供更有效的类似物,