Abstract
With the determination of the complete amino acid sequence of porcine glucagon by BROMER et al. (1957), the way was open for the chemical synthesis of this important peptide hormone. A synthesis would serve several purposes: it would, first of all, provide a classical proof of the proposed structure; secondly, it could lead to a large scale source of the hormone to replace the natural material, and, especially, it would provide a route to structural analogs designed to be inhibitors or superagonists that would be useful, both in defining the mechanism of action of glucagon and as potential clinical agents.
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Merrifield, R.B., Mojsov, S. (1983). The Chemical Synthesis of Glucagon. In: Lefèbvre, P.J. (eds) Glucagon I. Handbook of Experimental Pharmacology, vol 66 / 1. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-68866-9_2
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DOI: https://doi.org/10.1007/978-3-642-68866-9_2
Publisher Name: Springer, Berlin, Heidelberg
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