Chemical constituents from the fruits of Rhus typhina L. and their chemotaxonomic significance |
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Affiliation: | 1. Laboratory of Enzyme Technology, Department of Biotechnology, School of Food, Biotechnology and Development, Agricultural University of Athens, 75 Iera Odos Street, GR-11855 Athens, Greece;2. Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, 11942 Alkharj, KSA, Saudi Arabia;3. Department of Microbiology, College of Science, Al-Azhar University, Nasr City, 11884 Cairo, Egypt;4. Department of Pharmacognosy, College of Pharmacy, Alexandria University, Alexandria 21215, Egypt;1. Department of Bionics and Bioimpedance, University of Medical Sciences, Parkowa 2, 60-775 Poznań, Poland;2. Department of Orthopedics and Traumatology, University of Medical Sciences, 28 Czerwca 1956r., 135/147, 60-545 Poznań, Poland;3. Department of Rheumatology and Rehabilitation, University of Medical Sciences, 28 Czerwca 1956r., 135/147, 60-545 Poznań, Poland |
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Abstract: | This work describes the isolation and characterization of twenty-nine compounds from the fruits of Rhus typhina L., including eleven flavonoids (1–11), eleven phenols (12–22), two pentacyclic triterpenes (23–24), two organic acids (25–26), one lumichrome (27), one courmarin (28) and one pyrimidine (29) on the basis of their spectroscopic data. Compounds apigenin (1), daidzein (4), orobol (5), 3′, 5, 5′, 7-tetrahydroxyflavanone (6), naringenin (7), butein (8), (-)-catechin (9), quercetin-3-O-α-L-(3″-O-galloyl)-rhamnoside (11), 2-hydroxybenzoic acid (13), 4-hydroxybenzaldehyde (14), vanillin (15), methyl 3,4-dihydroxybenzoate (16), 3,5-dihydroxybenzamide (18), tyrosol (19), caffeic acid (20), 3-(2,4,6-trihydroxyphenyl)-1-(4-hydroxyphenyl)-propan-1-one (21), phlorizin (22), friedelin (23), oleanolic acid (24), 4,4-dimethyl-heptanedioic acid (25), anthranilic acid (26), lumichrome (27), scoparone (28) and uracil (29) have not been recorded before in this plant. This is the first report on the occurrence of compounds 4–7, 9, 11, 13–14, 16, 18–21, 25–29 from the genus Rhus. Moreover, the chemotaxonomic significance of these isolated compounds was also summarized. |
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Keywords: | Flavonoids Phenols Glycosides Chemotaxonomics IKGXIBQEEMLURG-HIOMCWGNSA-N AYMYWHCQALZEGT-ORCRQEGFSA-N GUAFOGOEJLSQBT-UHFFFAOYSA-N MWOOGOJBHIARFG-UHFFFAOYSA-N QAIPRVGONGVQAS-DUXPYHPUSA-N IOYHCQBYQJQBSK-UHFFFAOYSA-N YDUOHBXBLZGANF-UHFFFAOYSA-N LNTHITQWFMADLM-UHFFFAOYSA-N FBSFWRHWHYMIOG-UHFFFAOYSA-N REFJWTPEDVJJIY-UHFFFAOYSA-N IOUVKUPGCMBWBT-QNDFHXLGSA-N FTVWIRXFELQLPI-UHFFFAOYSA-N ZJTJUVIJVLLGSP-UHFFFAOYSA-N RGHHSNMVTDWUBI-UHFFFAOYSA-N ZQSIJRDFPHDXIC-UHFFFAOYSA-N YCCILVSKPBXVIP-UHFFFAOYSA-N MIJYXULNPSFWEK-YOQSOQNOSA-N JFLAOPHOUGDFGC-ILADGKKJSA-N PFTAWBLQPZVEMU-HIFRSBDPSA-N ISAKRJDGNUQOIC-UHFFFAOYSA-N CUFLZUDASVUNOE-UHFFFAOYSA-N KZNIFHPLKGYRTM-UHFFFAOYSA-N BGXMCVFPVOOLOC-UHFFFAOYSA-N AYHOUUNTAVCXBN-UHFFFAOYSA-N RWZYAGGXGHYGMB-UHFFFAOYSA-N YGSDEFSMJLZEOE-UHFFFAOYSA-N IYRMWMYZSQPJKC-UHFFFAOYSA-N PLYYMFBDRBSPJZ-UHFFFAOYSA-N PFZXVVZKPCFFPL-DMUHOSIPSA-N |
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