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ABSTRACT: Background
The α7 nicotinic acetylcholine receptor (nAChR) is an important molecular target in neuropsychiatry and oncology. Development of applicable highly specific radiotracers has been challenging due to comparably low protein expression. To identify novel ligands as candidates for positron emission tomography (PET), a library of diazabicyclononane compounds was screened regarding affinity and specificity towards α7 nAChRs. From these, [(18)F]NS14490 has been shown to yield reliable results in organ distribution studies; however, the radiosynthesis of [(18)F]NS14490 required optimization and automation to obtain the radiotracer in quantities allowing dynamic PET studies in piglets.Methods
Automated radiosynthesis of [(18)F]NS14490 has been performed by [(18)F]fluorinati
SUBMITTER: Rotering S
PROVIDER: S-EPMC4129469 | biostudies-literature | 2014
REPOSITORIES: biostudies-literature