Synthesis and properties of oxytocin analogues with high and selective natriuretic activity

Abstract
Deamino-6-carba-oxytocin analogues with modified aromatic amino acid in the position 2 were prepared by stepwise peptide synthesis in solution and cyclization in the last step. Some of the prepared analogues exhibit high and/or specific natriuretic activity. Structural requirements for this type biologic activity are discussed.

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