Literature DB >> 21426200

Natural products and ion channel pharmacology.

Russell W Teichert1, Baldomero M Olivera.   

Abstract

An accelerated rate of natural-product discovery is critical for the future of ion channel pharmacology. For the full potential of natural products to be realized, an interdisciplinary initiative is required that combines chemical ecology and ion channel physiology. A prime source of future drug leads targeted to ion channels is the vast assortment of compounds that mediate biotic interactions in the marine environment. pan class="Species">Many animals have evolved a chemical strategy to change the behavior of their class="Chemical">prey, class="Chemical">predators or comclass="Chemical">petitors, which aclass="Chemical">pclass="Chemical">pears to require a large set of ion channel-targeted comclass="Chemical">pounds acting in concert. Some of these comclass="Chemical">pounds (e.g., ziconotide [Prialt(®)]) have already found imclass="Chemical">portant biomedical aclass="Chemical">pclass="Chemical">plications. The elucidation of molecular mechanisms mediating biotic interactions should yield a rich stream of class="Chemical">potent and selective natural class="Chemical">products for the drug class="Chemical">piclass="Chemical">peline.

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Year:  2010        PMID: 21426200      PMCID: PMC4153603          DOI: 10.4155/fmc.10.31

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  65 in total

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  16 in total

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9.  A pain-inducing centipede toxin targets the heat activation machinery of nociceptor TRPV1.

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10.  Elucidation of the molecular envenomation strategy of the cone snail Conus geographus through transcriptome sequencing of its venom duct.

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