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- W2107040575 abstract "The synthesis of the hexapeptide Z-Tyr(SO-3)-Met-Gly-Trp-Met-Asp-NH2, representing the C-terminal sequence of cholecystokinin minus the C-terminal phenylalanyl residue is described. This peptide was shown to be the most potent cholecystokinin receptor antagonist in vitro described to date. It is also able to inhibit gastrin-induced acid secretion in vivo, in the rat and was proved to antagonize the action of the C-terminal octapeptide of cholecystokinin in the central nervous system." @default.
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- W2107040575 date "2009-01-12" @default.
- W2107040575 modified "2023-10-16" @default.
- W2107040575 title "Synthesis of Z-CCK-27-32-NH2, Z-Tyr(So3-)-Met-Gly-Trp-Met-Asp-NH2, a cholecystokinin receptor antagonist and an inhibitor of gastrin-induced acid secretion" @default.
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- W2107040575 doi "https://doi.org/10.1111/j.1399-3011.1985.tb03207.x" @default.
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