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Chemical constituents from Silene schimperiana Boiss. belonging to caryophyllaceae and their chemotaxonomic significance
Affiliation:1. College of Biological Resources and Environment Science, Qujing Normal University, Qujing 655011, China;2. Institute of Characteristic Medicinal Resource of Ethnic Minorities, Qujing Normal University, Qujing 655011, China;3. College of Physics and Electronic Engineering, Qujing Normal University, Qujing 655011, China;1. Université de Reims Champagne Ardenne, CNRS, ICMR, Reims, France;2. Université frères Mentouri-Constantine 1, Département de chimie, Laboratoire d′Obtention de Substances Thérapeutiques (LOST), Campus Chaabet-Ersas, 25000 Constantine, Algeria;1. Selcuk University, Science Faculty, Department of Biology, Campıus, Konya, Turkey;2. Centre of Marine Sciences, University of Algarve, Faculty of Sciences and Technology, Ed. 7, Campus of Gambelas, 8005-139, Faro, Portugal;3. School of Pharmacy, Universiti Sains Malaysia, Penang, Malaysia;4. Chemistry Department, College of Education, Salahaddin University, Erbil, Iraq;5. Department of Pharmacy, University “G. d’Annunzio” Chieti-Pescara, 66100, Chieti, Italy;6. Department of Health Sciences, Faculty of Science, University of Mauritius, 230, Réduit, Mauritius;7. REEF Environmental Consultancy, #2 Kamaraj Street, S.P. Nagar, Puducherry, 605 001, India
Abstract:Phytochemical investigation of Silene schimperiana Boiss. ethanolic extract led to the isolation of fifteen compounds (1–15). The isolated compounds were identified by their NMR, MS spectral data analyses and comparing with published data as: vanillic acid (1), ferulic acid (2), caffeic acid (3), ethyl ferulate (4), apigenin (5), hesperetin (6), diosmetin (7), luteolin (8), kaempferol (9), quercetin (10), ecdysterone (11), hesperedin (12), diosmin (13), kaempferol-3-O-rutinoside (14) and rutin (15). The lack of chemical and biological investigations on this plant encouraged us to carry out the above-mentioned work.
Keywords:Flavonoids  Ecdysterone  Phenolic acids
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