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Docking Studies, Synthesis, Characterization and Evaluation of Their Antioxidant and Cytotoxic Activities of Some Novel Isoxazole-Substituted 9-Anilinoacridine Derivatives

机译:一些新型异恶唑取代的9-苯胺基r啶衍生物的对接研究,合成,表征及其抗氧化和细胞毒活性的评价

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摘要

A convenient synthesis of novel isoxazole-substituted 9-anilinoacridine derivatives 5a–j was reported. The compounds were confirmed by physical and analytical data and screened for in vitro antioxidant activity by DPPH method, reducing power assay and total antioxidant capacity method. The cytotoxic activity of the compounds was also studied in HEp-2 cell line. The docking studies of the synthesized compounds were performed towards the key nucleoside dsDNA by using AutoDock vina 4.0 programme. All the isoxazole-substituted compounds have significant activities.
机译:据报道,新型异恶唑取代的9-苯胺基cr啶衍生物5a–j的合成简便。通过物理和分析数据确认了化合物,并通过DPPH法,还原力测定法和总抗氧化剂容量法筛选了体外抗氧化剂活性。还在HEp-2细胞系中研究了化合物的细胞毒性活性。通过使用AutoDock vina 4.0程序对关键核苷dsDNA进行了合成化合物的对接研究。所有异恶唑取代的化合物均具有明显的活性。

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