Synthesis and characterization of a sulfated and a non-sulfated cyclic CCK8 analogue functionalized with a chelating group for metal labelling

✍ Scribed by Stefania De Luca; Giancarlo Morelli

• Publisher: John Wiley and Sons
• Year: 2004
• Tongue: English
• Weight: 139 KB
• Volume: 10
• Category: Article
• ISSN: 1075-2617
• DOI: 10.1002/psc.527

✦ Synopsis

Abstract

Two cyclic peptides, cyclo^29, 34^[Dpr^29^, Lys^34^(DTPA‐Glu)]‐CCK8 (1) and cyclo^29, 34^[Tyr^27^(SO~3~H), Dpr^29^, Lys^34^(DTPA‐Glu)]‐CCK8 (2), bearing the chelating moiety DTPA‐Glu covalently bound to the Lys side chain have been synthesized by solid‐phase methodology. The presence in compound 2 of many acidic functions characteristic of the chelating agent increases the lability of the sulfate group on the Tyr side chain. This finding suggests that prolonged acid treatments should be avoided during the preparation of such peptides. Sulfation of cyclo^29, 34^[Dpr^29^, Lys^34^(DTPA‐Glu)]‐CCK8 was performed using a pyridine–SO~3~ complex as reagent. This reaction has been found to be the most suitable synthetic strategy for obtaining compound 2 in good yield. Cyclo^29, 34^[Tyr^27^(SO~3~H), Dpr^29^, Lys^34^(DTPA‐Glu)]‐CCK8 is a new promising CCK8 analogue, able to coordinate radioactive isotopes of metal ions such as ^111^In(III), and to bind, in a selective way, the CCK~A~‐R receptor. Copyright © 2003 European Peptide Society and John Wiley & Sons, Ltd.