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  • Spermatinamine, the first natural product inhibitor of isoprenylcysteine carboxyl methyltransferase, a new cancer target

    Author(s)
    Buchanan, Malcolm S
    Carroll, Anthony R
    Fechner, Gregory A
    Boyle, Anthony
    Simpson, Moana M
    Addepalli, Rama
    Avery, Vicky M
    Hooper, John NA
    Su, Nancy
    Chen, Huawei
    Quinn, Ronald J
    Griffith University Author(s)
    Quinn, Ronald J.
    Carroll, Anthony R.
    Avery, Vicky M.
    Year published
    2007
    Metadata
    Show full item record
    Abstract
    Isoprenylcysteine methyltransferase (Icmt) catalyzes the carboxyl methylation of oncogenic proteins in the final step of a series of post-translational modifications. The inhibition of Icmt provides an attractive and novel anticancer target. A natural product high-throughput screening campaign was conducted to discover inhibitors of Icmt. The Australian marine sponge, Pseudoceratina sp., yielded spermatinamine, a novel alkaloid with a bromotyrosyl-spermine-bromotyrosyl sequence, as the bioactive constituent. Its structure was determined by 1D and 2D NMR spectroscopy. Spermatinamine is the first natural product inhibitor ...
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    Isoprenylcysteine methyltransferase (Icmt) catalyzes the carboxyl methylation of oncogenic proteins in the final step of a series of post-translational modifications. The inhibition of Icmt provides an attractive and novel anticancer target. A natural product high-throughput screening campaign was conducted to discover inhibitors of Icmt. The Australian marine sponge, Pseudoceratina sp., yielded spermatinamine, a novel alkaloid with a bromotyrosyl-spermine-bromotyrosyl sequence, as the bioactive constituent. Its structure was determined by 1D and 2D NMR spectroscopy. Spermatinamine is the first natural product inhibitor of Icmt.
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    Journal Title
    Bioorganic & Medicinal Chemistry Letters
    Volume
    17
    Issue
    24
    Publisher URI
    http://www.elsevier.com/wps/find/journaldescription.cws_home/972/description#description
    DOI
    https://doi.org/10.1016/j.bmcl.2007.10.021
    Subject
    Medicinal and biomolecular chemistry
    Organic chemistry
    Pharmacology and pharmaceutical sciences
    Publication URI
    http://hdl.handle.net/10072/17201
    Collection
    • Journal articles

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