| Literature DB >> 17964784 |
Malcolm S Buchanan1, Anthony R Carroll, Gregory A Fechner, Anthony Boyle, Moana M Simpson, Rama Addepalli, Vicky M Avery, John N A Hooper, Nancy Su, Huawei Chen, Ronald J Quinn.
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 of Icmt.Entities:
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Year: 2007 PMID: 17964784 DOI: 10.1016/j.bmcl.2007.10.021
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823