Acyl Quinic Acid Derivatives Screened Out from by SOD-Affinity Ultrafiltration LC-MS and Their Antioxidative and Hepatoprotective Activities.

Linn. has been utilized both in the food industry and as a traditional medicine for various ailments, while the responsible chemical components and action mechanisms of its antioxidative and hepatoprotective activities remain unclear. In this work, at least 17 quinic acid derivatives as potential ligands for the superoxide dismutase (SOD) enzyme from   L. were screened out using the bio-affinity ultrafiltration with liquid chromatography mass spectrometry (UF-LC/MS), and 12 of them (-), including, three new ones (-), were further isolated by phytochemical methods and identified by high resolution electrospray ionization mass spectrometry (HR-ESI-MS) and extensive nuclear magnetic resonance (NMR) spectroscopic analysis. All of these isolated compounds were evaluated for their antioxidant activities by the 1,1-diphenyl-2-picrylhydrazyl (DPPH) and ferric-reducing antioxidant power (FRAP) methods. As a result, compounds and - displayed similar or better antioxidant activities compared to vitamin C, which is in good agreement with the bio-affinity ultrafiltration with SOD enzyme. Then, these compounds, and -, with better antioxidant activity were further explored to protect the L02 cells from HO-induced oxidative injury by reducing the reactive oxygen species (ROS) and Malondialdehyde (MDA) production and activating the SOD enzyme. To the best of our knowledge, this is the first report to use an efficient ultrafiltration approach with SOD for the rapid screening and identification of the SOD ligands directly from a complex crude extract of , and to reveal its corresponding active compounds with good antioxidative and hepatoprotective activities.