Synthesis of [U-14C]Arg labelled decapeptide cetrorelix, a novel lutenizing hormone - releasing hormone antagonist
作者:Mathias Locher、James Johnston、Thomas Müller、Harald O. Borbe、Bernhard Kutscher、Jürgen Engel
DOI:10.1002/jlcr.2580341113
日期:1994.11
The decapeptide cetrorelix is a novel luteinizing hormone — releasing hormone (LH-RH) antagonist. For nonclinical studies concerning absorption, distribution, metabolism and excretion (ADME) in animals the [14C]-lebelled compound is essential. Therefore, [U-14C]Arg cetrorelix acetate salt was synthesized by Amersham International, Buckinghamshire (England) from precursor peptides provided by Degussa AG, Hanau-Wolfgang (Germany). [U-14C]Arg labelled cetrorelix peptide base has a specific activity of 8.13 MBq/mg (220 μCi/mg) and a molecular weight of 1442.6 g/mol at this specific activity. The chemical and radiochemical purity (92.2 % decapeptide content and 97.6%, respectively) determined by HPLC is suitable for nonclinical investigations.