Tracers / [123I]PARPi-01

[123I]PARPi-01

Also written as [I-123]PARPi-01
Radionuclide
I-123 t½ 792 min
Modality
Therapy
Production route
Stage
preclinical study
Syntheses indexed
1

What it is

Compound class
PARP inhibitor (Olaparib derivative)
Target / mechanism
PARP1 (Poly (ADP-ribose)-Polymerase 1) targeting Auger emitter therapy PMID 36104637
Clinical application
SPECT/CT imaging in triple-negative breast cancer xenograft model to guide theranostic Auger emitter therapy PMID 36104637
Theranostic pair

Regulatory status

FDA
EMA (centralised)
Other approvals
Brand names

Clinical use

Typical injected activity
Uptake time

Reported in the literature. Not a dosing recommendation.

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
Manual synthesisHPLC+SPE78 ± 12%>95%Tributyl stannylated derivative of Olaparib36104637
2022 EJNMMI Res
Radiolabelling was conducted as previously described [17] — The resulting overall radiochemical yield was 78 ± 12% with purities of > 95%.

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Notes

Added at stage 22: promoted from 'Reported once' (single-article, no diagnostic pair at discovery) because a full-text synthesis with extracted data exists in parsed-therapy.xlsx -- PMID(s): 36104637. Target/mechanism, clinical application, indications, approval and precursor fields still need per-agent research and are intentionally left empty. Stage set/updated at stage 23 from PMID 36104637: 'In this study, a theranostic approach was investigated in a TNBC xenografted mouse model by radiolabelling a close derivative of a PARPi Olaparib (termed PARPi-01) with the Auger emitters 123/125I.'.