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18F-Talazoparib (also known as [18F]talazoparib or 18F-TZ) is an 18F-radiolabeled isotopologue of the potent poly(ADP-ribose) polymerase (PARP) inhibitor talazoparib. It is developed as a positron emission tomography (PET) imaging radiotracer to non-invasively evaluate PARP1 and PARP2 expression levels, assess drug-target engagement, and aid in patient selection and therapy dose optimization for PARP inhibitor therapies. Synthesized via copper-mediated radiofluorination, 18F-talazoparib exhibits high affinity and specificity for PARP1/2, demonstrating blockable uptake in PARP-expressing tumor cells and favorable tumor-to-blood ratios in preclinical models of breast, prostate, ovarian, and pancreatic cancers.
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