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. 1978 Feb;359(2):147-53.

[Synthesis of human [11-leucine]minigastrin I.--I. Preparation of the fully protected tridecapeptide amide (author's transl)]

[Article in German]
L Moroder, F Drees, E Jaeger, E Wünsch
  • PMID: 649049

[Synthesis of human [11-leucine]minigastrin I.--I. Preparation of the fully protected tridecapeptide amide (author's transl)]

[Article in German]
L Moroder et al. Hoppe Seylers Z Physiol Chem. 1978 Feb.

Abstract

The synthesis of the tridecapeptide amide corresponding to and 11-leucine analog of human minigastrin I is decribed. The fully protected peptide derivative was obtained by assembly of three suitably protected fragments corresponding to the sequences 1-6, 7-9 and 10-13 by the carbodiimide/N-hydroxysuccinimide method.

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