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Identification and characterization of potent small molecule inhibitor of hemorrhagic fever New World arenaviruses

  1. Author:
    Bolken, T. C.
    Laquerre, S.
    Zhang, Y. M.
    Bailey, T. R.
    Pevear, D. C.
    Kickner, S. S.
    Sperzel, L. E.
    Jones, K. F.
    Warren, T. K.
    Lund, S. A.
    Kirkwood-Watts, D. L.
    King, D. S.
    Shurtleff, A. C.
    Guttieri, M. C.
    Deng, Y. J.
    Bleam, M.
    Hruby, D. E.
  2. Author Address

    SIGA Technol Inc, Corvallis, OR 97333 USA. ViroPharma Inc, Exton, PA 19341 USA. USA, Med Res Inst Infect Dis, Dept Mol Virol, Frederick, MD 21702 USA.;Hruby, DE, SIGA Technol Inc, 4575 SW Res Way, Corvallis, OR 97333 USA.;dhruby@sgph.com
    1. Year: 2006
    2. Date: Feb
  1. Journal: Antiviral Research
    1. 69
    2. 2
    3. Pages: 86-97
  2. Type of Article: Article
  3. ISSN: 0166-3542
  1. Abstract:

    Category A arenaviruses as defined by the National Institute of Allergy and Infectious Diseases (NIAID) are human pathogens that could be weaponized by bioterrorists. Many of these deadly viruses require biosafety level-4 (BSL-4) containment for all laboratory work, which limits traditional laboratory high-throughput screening (HTS) for identification of small molecule inhibitors. For those reasons, a related BSL-2 New World arenavirus, Tacaribe virus, 67-78% identical to Junin virus at the amino acid level, was used in a HTS campaign where approximately 400,000 small molecule compounds were screened in a Tacaribe virus-induced cytopathic effect (CPE) assay. Compounds identified in this screen showed antiviral activity and specificity against not only Tacaribe virus, but also the Category A New World arenaviruses (Junin, Machupo, and Guanarito). Drug resistant variants were isolated, suggesting that these compounds act through inhibition of a viral protein, the viral glycoprotein (GP2), and not through cellular toxicity mechanisms. A lead compound, ST-294, has been chosen for drug development. This potent and selective compound, with good bioavailability, demonstrated protective anti-viral efficacy in a Tacaribe mouse challenge model. This series of compounds represent a new class of inhibitors that may warrant further development for potential inclusion in a strategic stockpile. (c) 2005 Elsevier B.V. All rights reserved.

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External Sources

  1. DOI: 10.1016/j.antiviral.2005.10.008
  2. WOS: 000235418100005

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