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Synthesis and Characterization of the Pain-Killing Peptide Grammostola spatulata Analgesic Factor (GsAF-1) Containing Three Disulfide Bonds

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Peptides: The Wave of the Future

Part of the book series: American Peptide Symposia ((APSY,volume 7))

Abstract

Recent work at AstraZeneca resulted in the discovery of novel pain-killing peptides from the venom of the Chilean pink tarantula [1–3]. These peptides, designated Grammostola spatulata analgesic factors (GsAF), were found effective in a variety of animal models of moderate-to-severe pain. They were also found to exhibit activity in models of neuropathic pain, and as such represent a potentially interesting approach to the amelioration of pain associated with cancer and the post-operative surgical period.

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References

  1. Lampe, R.A., Sachs, F., US Patent 5,756,663, May 26, 1998.

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  2. Lampe, R.A. US Patent 5,776,896, July 7, 1998.

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  3. Lampe, R.A. US Patent 5,807,821, Sept. 15, 1998.

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© 2001 Springer Science+Business Media Dordrecht

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Liu, Rq., Jacobs, R.T., Spreen, R.C., Barany, G. (2001). Synthesis and Characterization of the Pain-Killing Peptide Grammostola spatulata Analgesic Factor (GsAF-1) Containing Three Disulfide Bonds. In: Lebl, M., Houghten, R.A. (eds) Peptides: The Wave of the Future. American Peptide Symposia, vol 7. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-0464-0_191

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  • DOI: https://doi.org/10.1007/978-94-010-0464-0_191

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-3905-5

  • Online ISBN: 978-94-010-0464-0

  • eBook Packages: Springer Book Archive

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