| Literature DB >> 11150708 |
W B Mathews1, U Scheffel, P Finley, H T Ravert, R A Frank, M Rinaldi-Carmona, F Barth, R F Dannals.
Abstract
ABSTRACT. [(18)F] SR144385 and [(18)F] SR147963 were synthesized in a multistep reaction in which fluorine-18 was introduced by nucleophilic halogen displacement on a bromo precursor. The fluorine-18-labeled intermediate was deprotected and coupled with the appropriate alkyl amine to give the final products. Both radioligands had appropriate regional brain distribution for cannabinoid receptors with a target to nontarget ratio of 1.7 for [(18)F] SR147963 and 2.5 for [(18)F] SR144385 at 60 and 90 min postinjection, respectively. The uptake of both tracers was blocked with a 1 mg/kg dose of SR141716A.Entities:
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Year: 2000 PMID: 11150708 DOI: 10.1016/s0969-8051(00)00152-9
Source DB: PubMed Journal: Nucl Med Biol ISSN: 0969-8051 Impact factor: 2.408