SETT ATT FRAMSTELLA NYA AUALOGER AV DEAMINO-VASOPRESSIN MED MODIFIERAD DISALFIDBRYGGA

摘要

Stepwise synthesis in solution and cyclization by means of active esters or another method suitable for peptide bond formation were used to prepare analogues of deamino-vasopressin with the disulphide bridge altered to the thioether group. In sequence position 8 of the peptide chain the analogs differed by the nature of basic amino acid. Typical vasopressin-like activities, mainly antidiuretic, were very high in these analogs; of particular importance will be their haemodynamic activity.