| Literature DB >> 214557 |
M Bodansky, S Natarajan, J D Gardner, G M Makhlouf, S I Said.
Abstract
The 23-peptide 15-lysine-secretin-(5-27) [S(5-27)] was synthesized on an insoluble support. The residue in position 15 of secretin, aspartic acid, was replaced by lysine, which occupies that position in the vasoactive intestinal polypeptide (VIP), a member of the secretin family. The resulting analogue showed increased VIP-like activity on smooth muscle preparations and unaltered secretin-like activity on pancreatic juice secretion in the rat. The affinity of the new analogue was high-affinity secretin receptors in acinar cells from guinea pig pancreas was less than that of S(5-27) but was higher than that of S(5-27) for high-affinity VIP receptors in the same cells.Entities:
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Year: 1978 PMID： 214557 DOI： 10.1021/jm00209a018
Source DB: PubMed Journal: J Med Chem ISSN： 0022-2623 Impact factor: 7.446