Synthesis, crystal structure, superoxide scavenging activity, anticancer and docking studies of novel adamantyl nitroxide derivatives

• Published in: Journal of molecular structure 2016-03, Vol.1108, p.611-617
• Main Authors: Zhu, Xiao-he, Sun, Jin, Wang, Shan, Bu, Wei, Yao, Min-na, Gao, Kai, Song, Ying, Zhao, Jin-yi, Lu, Cheng-tao, Zhang, En-hu, Yang, Zhi-fu, Wen, Ai-dong
• Format: Article
• Language: English
• Subjects: Adamantyl nitroxide; Anticancer; Anticancer properties; Antiproliferatives; Crystal structure; Derivatives; Docking; Docking study; Mathematical analysis; Molecular structure; Scavenging; Superoxide scavenging activity
• ISSN: 0022-2860; 1872-8014
• DOI: 10.1016/j.molstruc.2015.12.048

A novel adamantyl nitroxide derivatives has been synthesized and characterized by IR, ESI-MS and elemental analysis. Quantum chemical calculations have also been performed to calculate the molecular geometry using density functional theory (B3LYP) with the 6-31G (d,p) basis set. The calculated results showed that the optimized geometry can well reproduce the crystal structure. The antioxidant and antiproliferative activity were evaluated by superoxide (NBT) and MTT assay. The adamantyl nitroxide derivatives exhibited stronger scavenging ability towards O2· − radicals when compared to Vitamin C, and demonstrated a remarked anticancer activity against all the tested cell lines, especially Bel-7404 cells with IC50 of 43.3 μM, compared to the positive control Sorafenib (IC50 = 92.0 μM). The results of molecular docking within EGFR using AutoDock confirmed that the titled compound favorably fitted into the ATP binding site of EGFR and would be a potential anticancer agent. [Display omitted] •A novel adamantyl nitroxide derivatives was synthesized and characterized.•The molecular structure was determined by X-ray diffraction and DFT method.•The antioxidant and antiproliferative activity were carried out.•The docking studies suggested that the compound would be a potential anticancer agent.