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Characterization of inhibitory constituents of NO production from Catalpa ovata using LC-MS coupled with a cell-based assay
Affiliation:1. Institute of Genomic Cohort, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea;2. Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea;3. Department of Preventive Medicine, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea;1. Department of Chemistry, Shahid Bahonar University of Kerman, Kerman, Iran;2. Young Research Society, Shahid Bahonar University of Kerman, Kerman, Iran;3. Department of Biotechnology, Institute of Science, High Technology and Environmental Science, Graduate University of Advance Technology, Kerman, Iran
Abstract:An effective screening method for inhibitors of NO production in natural products using LC-QTOF MS/MS coupled with a cell-based assay was proposed. The ethyl acetate fraction of Catalpa ovata exhibited a strong inhibitory effect on NO production in lipopolysaccharide-induced BV2 microglia cells. We attempted to identify the active constituents of C. ovata by using LC-QTOF MS/MS coupled with a cell-based assay. Peaks at approximately 14–15 min on the MS chromatogram were estimated to be the bioactive constituents. A new iridoid compound, 6-O-trans-feruloyl-3β-hydroxy-7-deoxyrehamaglutin A (4), and nine known compounds (13, 510) were isolated from the ethyl acetate fraction of C. ovata by repeated column chromatography. Compounds 3, 4, 5, 7, and 8 significantly attenuated lipopolysaccharide-stimulated NO production in BV2 cells. Our results indicate that LC-QTOF MS/MS coupled with a cell-based NO production inhibitory assay successfully predicted active compounds without a time-consuming isolation process.
Keywords:Bignoniaceae  Chemical profile  LC-QTOF MS/MS  Anti-inflammatory  NO production  LPS
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