Tracers / [68Ga]AAZTA-FAPI-46

[68Ga]AAZTA-FAPI-46

Also written as [Ga-68]Ga-AAZTA-FAPI-46
Radionuclide
Ga-68 t½ 67.71 min
Modality
Therapy
Production route
Stage
preclinical study
Syntheses indexed
2

What it is

Compound class
AAZTA-conjugated FAP inhibitor (FAPI-46-derived)
Target / mechanism
Fibroblast activation protein (FAP) inhibitor targeting FAP-expressing tumor stroma PMID 40762892
Clinical application
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
Scintomics GallElut
Scintomics
custom manifoldSPE84.97 ± 1.37%greater than 98%AAZTA-FAPI-4640762892
2025 EJNMMI Radiopharm Chem
The preparation of [68Ga]Ga-AAZTA-FAPI-46 was automated on a GallElut+ system (Scintomics, Germany). — The radiochemical yield was 84.97 ± 1.37%.
Manual synthesisSPEgreater than 98%AAZTA-FAPI-4640762892
2025 EJNMMI Radiopharm Chem
Gallium-68 manual radiolabelling

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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): 40762892. 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 40762892: 'AAZTA-FAPI-46'. Stage set/updated at stage 23 from PMID 40762892: 'Preclinical evaluation of [68Ga]Ga-AAZTA-FAPI-46: a novel PET tracer for targeting fibroblast activation protein (FAP).'.