[Structure-activity Relationship of Human Calcitonin. III. Biological Activity of Synthetic Analogues with Shortened or Terminally Modified Peptide Chains (author's Transl)]
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Assays of 8 synthetic analogues of human calcitonin in rats showed that their hypocalcaemic activity was drastically reduced by deletion of the C-terminal amide group, chain-shortening or opening of the disulphide ring, but unaffected or enhanced by modification of the N-terminal amino group.
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