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  • Denhaminols A−H, Dihydro-β-agarofurans from the Endemic Australian Rainforest Plant Denhamia celastroides

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    Author(s)
    Levrier, Claire
    Sadowski, Martin C
    Nelson, Colleen C
    Healy, Peter C
    Davis, Rohan A
    Griffith University Author(s)
    Healy, Peter C.
    Davis, Rohan A.
    Year published
    2015
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    Abstract
    Eight new dihydro-߭agarofurans, denhaminols A-H (1-8), were isolated from the leaves of the Australian rainforest tree Denhamia celastroides. The chemical structures of 1-8 were elucidated following analysis of 1D/2D NMR and MS data. The absolute configuration of denhaminol A (1) was determined by single-crystal X-ray crystallography. All compounds were evaluated for cytotoxic activity against the human prostate cancer cell line LNCaP, using live-cell imaging and metabolic assays. Denhaminols A (1) and G (7) were also tested for their effects on the lipid content of LNCaP cells. This is the first report of secondary metabolites ...
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    Eight new dihydro-߭agarofurans, denhaminols A-H (1-8), were isolated from the leaves of the Australian rainforest tree Denhamia celastroides. The chemical structures of 1-8 were elucidated following analysis of 1D/2D NMR and MS data. The absolute configuration of denhaminol A (1) was determined by single-crystal X-ray crystallography. All compounds were evaluated for cytotoxic activity against the human prostate cancer cell line LNCaP, using live-cell imaging and metabolic assays. Denhaminols A (1) and G (7) were also tested for their effects on the lipid content of LNCaP cells. This is the first report of secondary metabolites from D. celastroides.
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    Journal Title
    Journal of Natural Products
    Volume
    78
    Issue
    1
    DOI
    https://doi.org/10.1021/np500740f
    Copyright Statement
    © 2015 American Chemical Society and American Society of Pharmacognosy. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
    Subject
    Chemical sciences
    Biologically active molecules
    Biological sciences
    Biomedical and clinical sciences
    Publication URI
    http://hdl.handle.net/10072/69325
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    • Journal articles

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