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18F-OGA-1 is a radiopharmaceutical agent developed for positron emission tomography (PET) imaging. It targets O-linked-β-N-acetyl-glucosamine hydrolase (OGA) in the brain, an enzyme involved in the posttranslational modification of tau protein, which is a biomarker in Alzheimer's disease. OGA inhibition is believed to reduce tau aggregation, which is associated with neurodegenerative diseases. With a half-life of approximately 110 minutes, this fluorine-18 labeled compound is suitable for diagnostic neuroimaging applications.
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