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    Antiplasmodial Quinonesfrom Pentaslongiflora and Pentas lanceolata

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    Date
    2012-01
    Author
    Milkyas Endale.
    Alao John Patrick.
    Akala Hoseah M.
    Rono Nelson K.
    Eyase Fredrick L.
    Derese Solomon.
    Ndakala Albert.
    Mbugua Martin Njogu.
    Sunnerhagen Per.
    Erdelyi Mate.
    Yenesew Abiy.
    Type
    Article
    Language
    en
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    Abstract
    The dichloromethane/methanol (1:1) extracts of the roots of Pentas longiflora and Pentas lanceolata showed low micromolar (IC50=0.9–3µg/mL) in vitro antiplasmodial activity against chloroquineresistant (W2) and chloroquine-sensitive (D6) strains of Plasmodium falciparum. Chromatographic separation of the extract of Pentas longiflora led to the isolation of the pyranonaphthoquinones pentalongin (1) and psychorubrin (2) with IC50 values below 1µg/mL and the naphthalene derivative mollugin (3), which showed marginal activity. Similar treatment of Pentas lanceolata led to the isolation of eight anthraquinones (4–11,IC50=5–31µg/mL) of which one is new (5,6-dihydroxydamnacanthol, 11), while three– nordamnacanthal (7), lucidin-ω-methyl ether (9), and damnacanthol (10)– are reported here for the first time from the genus Pentas. The compounds were identified by NMR and mass spectroscopic techniques. Supportinginformation available online at http://www.thieme-connect.de/ejournals/toc/ plantamedic
    URI
    http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/9861
    http://www.ncbi.nlm.nih.gov/pubmed/21979929
    Citation
    Planta Med. 2012 Jan;78(1):31-5.
    Publisher
    Chemistry
    Subject
    Pentas longiflora
    Pentas lanceolata
    Pentas longiflora
    Rubiaceae
    anthraquinone
    5,6‑dihydroxydamnacanthol‑pyranonaphthoquinone
    malaria
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    • Faculty of Science & Technology (FST) [4211]

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