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Designing Activity and Receptor Selectivity in Cyclic Peptide Hormone Analogs

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Design and Synthesis of Organic Molecules Based on Molecular Recognition

Abstract

Peptide hormones often use only a small section of about five amino acid residues in the middle of a chain to transduce information (Fig. 1).

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References

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Author information

Authors and Affiliations

  1. Institut für Organische Chemie, J. W. Goethe-Universität, Niederurseler Hang, D-6000, Frankfurt 50, Germany

    Horst Kessler

Authors
  1. Horst Kessler
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Editor information

Editors and Affiliations

  1. Fakulteit der Wetenschappen, Organische Chemie, Vrije Universiteit Brussels, Pleinlaan 2, B-1050, Brussels, Belgium

    Georges Van Binst

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© 1986 Springer-Verlag Berlin Heidelberg

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Kessler, H. (1986). Designing Activity and Receptor Selectivity in Cyclic Peptide Hormone Analogs. In: Van Binst, G. (eds) Design and Synthesis of Organic Molecules Based on Molecular Recognition. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-70926-5_24

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  • DOI: https://doi.org/10.1007/978-3-642-70926-5_24

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-70928-9

  • Online ISBN: 978-3-642-70926-5

  • eBook Packages: Springer Book Archive

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