Structure-activity relationships of C-terminal tri- and tetrapeptide fragments that inhibit gastrin activity
A series of tri- and tetrapeptide derivatives, analogues of the gastrin C-terminal region with no phenylalanine residue, were synthesized. These peptides were tested for their ability to inhibit gastrin-stimulated acid secretion in vivo as well as binding
Synthesis and biological activity of new peptide segments of gastrin exhibiting gastrin antagonist property
A series of C-terminal peptide segments of gastrin, i.e., (tert-butyloxycarbonyl)-L-tryptophyl-L-methionyl-L-aspartic acid amide, (tert-butyloxycarbonyl-glycyl-L-tryptophyl-L-methionyl-L-aspartic acid amide, (tert-butyloxy-carbonyl)-L-tyrosyl-glycyl-L-try
Martinez,Magous,Lignon,Laur,Castro,Bali
p. 1597 - 1601
(2007/10/02)
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