Tracers / [125I]PARPi-01

[125I]PARPi-01

Radionuclide
I-125 t½ 85666 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) PMID 36104637
Clinical application
PARP targeted Auger emitter therapy for triple-negative breast cancer 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. Compound class inferred from precursor name (not stated outright) -- PMID 36104637: 'Tributyl stannylated derivative of Olaparib'. 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.'.