Journal article
[18F]Fluoro-β-fluoromethylene-m-tyrosine analogs, potential PET agents for presynaptic dopamine terminals : synthesis and spectroscopic characterization
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, Vol.43(8), pp.969-977
1992
DOI: 10.1016/0883-2889(92)90215-Z
PMID: 1330983
Abstract
FMMT was prepared by the direct reaction of FMMT with [18F]acetylhypofluorite (AcOF) resulting into three product isomers. Extensive 1H, 13C and 19F-NMR spectroscopic analysis identify these products to be 2-fluoro, 6-fluoro-FMMT and 2,6-difluoro-FMMT. The HPLC isolated radiochemical EOB yields of these products were 22, 25 and 14%, respectively, based on starting [18F]AcOF. The specific activity at the end of a synthesis time of an hour was ca 200 mCi/mmol. With the possible advantage of “metabolic trapping” in dopamine nerve terminals via covalent binding to MAO and reduced metabolite formation, [18F]F-FMMT may potentially be the optimal PET tracer for CNS dopamine nerve terminals.
Details
- Title: Subtitle
- [18F]Fluoro-β-fluoromethylene-m-tyrosine analogs, potential PET agents for presynaptic dopamine terminals : synthesis and spectroscopic characterization
- Creators
- D MURALI - Univ. Wisconsin, dep. medical physics, Madison WI 53706, United StatesO. T DEJESUS - Univ. Wisconsin, dep. medical physics, Madison WI 53706, United StatesJ. J SUNDERLAND - Univ. Wisconsin, dep. medical physics, Madison WI 53706, United StatesR. J NICKLES - Univ. Wisconsin, dep. medical physics, Madison WI 53706, United States
- Resource Type
- Journal article
- Publication Details
- International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, Vol.43(8), pp.969-977
- Publisher
- Pergamon; Oxford
- DOI
- 10.1016/0883-2889(92)90215-Z
- PMID
- 1330983
- ISSN
- 0883-2889
- Language
- English
- Date published
- 1992
- Academic Unit
- Radiology; Physics and Astronomy; Radiation Oncology
- Record Identifier
- 9984046827902771
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