Article ID Journal Published Year Pages File Type
10916069 Nuclear Medicine and Biology 2013 9 Pages PDF
Abstract
The novel PET tracer, [18F]FMePhe, is readily synthesized in good yield from a cyclic sulfamidate precursor. Biodistribution and microPET studies in the DBT model demonstrate good tumor to tissue ratios and tumor visualization, with enantiomer [18F]9a having higher tumor uptake. However, the brain availability of both enantiomers was lower than expected for system L substrates, suggesting the [18F]fluorine group in the β-position affects uptake of these compounds by system L transporters.
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