Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55311
Title: Antimalarial polyoxygenated and prenylated xanthones from the leaves and branches of Garcinia mckeaniana
Authors: Chiramet Auranwiwat
Surat Laphookhieo
Roonglawan Rattanajak
Sumalee Kamchonwongpaisan
Stephen G. Pyne
Thunwadee Ritthiwigrom
Keywords: Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Jan-2016
Abstract: © 2016 Elsevier Ltd The first phytochemical investigation of the leaf and branch extracts of Garcinia mckeaniana has led to the isolation and characterization of five new polyoxygenated and prenylated xanthones, mckeanianones A-E (1–5), and one new biflavone, mckeaniabiflavone (6), together with 13 known compounds (7–19). The diprenylated pyrano-xanthones (1–3) and the biflavone (6) were isolated from the leaves while the monoprenylated xanthones (4 and 5) were isolated from the branches. The structures of all isolated compounds were elucidated based on spectroscopic methods and were evaluated for their antimalarial activities against the Plasmodium falciparum strains, TM4 (drug sensitive strain) and K1 (a multidrug resistant strain), and cytotoxicity against a Vero cell line (African green monkey kidney epithelial cells). The pyrano-xanthones (1–3, 7 and 8), having two isoprene units, were generally the most active compounds with IC50values in the range of 6.0±1.1_8.5±1.2 and 3.6±1.7_7.3±1.2 μM, respectively against the TM4 and K1 strains. Of these compounds 2, 3 and 8 were 2–5 times less cytotoxic against a Vero cell line (IC50values of 12.6±0.9, 29.5±3.9 and 13.2±4.6 μM, respectively) in comparison with their antiplasmodial activities.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84988835934&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/55311
ISSN: 14645416
00404020
Appears in Collections:CMUL: Journal Articles

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