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Title: | Phenylpropanoids and furanocoumarins as antibacterial and antimalarial constituents of the Bhutanese medicinal plant Pleurospermum amabile |
Authors: | Wangchuk P. Pyne S.G. Keller P.A. ITaweechotipatr M. Kamchonwongpaisan S. |
Keywords: | bergapten cycloguanil elemicin eugenol folic acid antagonist furocoumarin derivative isoapiol isopimpinellin myristicin oxypeucedanin phenyl group phenylpropanoid derivative plant extract Pleurospermum amabile extract psoralen pyrimethamine unclassified drug animal cell antibacterial activity antimalarial activity article Bacillus subtilis Bhutan controlled study drug isolation human human cell medicinal plant nonhuman phytochemistry Plasmodium Pleurospermum amabile Animals Anti-Bacterial Agents Antifungal Agents Antimalarials Apiaceae Bacteria Bhutan Candida Cercopithecus aethiops Molecular Structure Plants, Medicinal Plasmodium falciparum Propanols Psoralens Vero Cells |
Issue Date: | 2014 |
Abstract: | With the objective of determining safety and verifying the traditional uses of the Bhutanese medicinal plant, Pleurospermum amabile Craib & W. W. Smith, we investigated its crude extracts and the isolated phytochemicals for their biological activities. Four phenylpropanoids [(E)-isomyristicin (1), (E)-isoapiol (2 ), methyl eugenol (3) and (E)-isoelemicin (4)] and six furanocoumarins [psoralen (5), bergapten (6), isoimperatorin (7), isopimpinellin (8 ), oxypeucedanin hydrate (9) and oxypeucedanin methanolate (10 )] were isolated from this plant. Among the test samples, compound 10 showed weak antibacterial activity against Bacillus subtilis and best antimalarial activity against the Plasmodium falciparum strains, TM4/8.2 (chloroquine and antifolate sensitive) and K1CB1 (multidrug resistant). None of the test samples showed cytotoxicity. This study generated scientific data that support the traditional medical uses of the plant. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/14022 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84905105669&doi=10.1177%2f1934578x1400900719&partnerID=40&md5=c221e6ea9a07d1da5207bbc4dc70610c |
ISSN: | 1934578X |
Appears in Collections: | Scopus 1983-2021 |
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