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The synthesis by conventional methods of the peptides Z-Asp-Cys-NH 2 , Z-Asp-Gly-Cys-NH 2  , Z-Glu-Gly-Cys-NH 2 , Z-His-Ala-Gly-Gly-Cys-NH 2 , Z-His-Ala-Asp-Gly-Cys-NH 2  and Z-His-Ala-Asp- Gly-OCH 3  is described. Cystin was used for SH-protection; reduction of the disulfides was performed by mercaptoethanol. The hydrolytic activity of these peptides with p-nitrophenylacetate as substrate was compared with the activity of a number of peptides described in the literature.

Synthese und katalytische Eigenschaften hydrolytisch aktiver Peptide /Synthesis and Catalytic Properties of Peptides with Hydrolytic Activity