Refereed journal article or data article (A1)

Synthesis and biological evaluation of novel I-123-labeled 4-(4-iodophenyl)butanoyl-L-prolyl-(2S)-pyrrolidines for imaging prolyl oligopeptidase in vivo




List of AuthorsKallinen A, Todorov B, Kallionpaa R, Back S, Sarparanta M, Raki M, Garcia-Horsman JA, Bergstrom KA, Wallen EAA, Mannisto PT, Airaksinen AJ

PublisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER

Publication year2014

JournalEuropean Journal of Medicinal Chemistry

Journal name in sourceEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Journal acronymEUR J MED CHEM

Volume number79

Start page436

End page445

Number of pages10

ISSN0223-5234

DOIhttp://dx.doi.org/10.1016/j.ejmech.2014.04.014


Abstract
Prolyl oligopeptidase (POP) may be associated with neuromodulation and development of neurodegenerative diseases and it was recently shown to participate in the inflammatory cascade along with matrix metalloproteinases. Radiotracers, which can be used for non-invasive imaging, are needed for investigating the role of POP in normal physiology and in pathophysiological conditions in vivo. We synthesized two novel POP-specific I-123-radiolabeled 4-phenylbutanoyl-L-prolyl-pyrrolidines of which 4(4-[I-123]iodophenyl)butanoyl-r-proly1-2(S)-cyanopyrrolidine ([I-123]2f, K-i = 4.2 nM) was selected. The selected compound has an electrophilic cyano group that is known to increase the dissociation time of POP inhibitors. [I-123]2f was synthesized in high radiochemical yield and purity (87 4%, >99%, respectively) and with a specific activity of 456 98 GBq/mu mol. [1231]2f was evaluated in healthy mice (C57BI/6JRccHsd) by ex vivo biodistribution studies and SPECT imaging. Pretreatment with the known inhibitor 4-phenylbutanoyl-L-prolyl-(2S)-cyanopyrrolidine (KYP-2047, 2d, K-i = 0.023 nM) showed that binding of [I-123]2f was POP specific. In addition, [1231]2f was evaluated in models of neuroinflammation and acute localized inflammation. A minor increase in binding of [I-123]2f was observed in the inflamed region in the acute localized inflammation model. Similar increase in binding was not observed in the neuroinflammation model. (c) 2014 Elsevier Masson SAS. All rights reserved.


Last updated on 2023-25-03 at 21:31