Tracers / [18F]AlF-H3RESCA-FAPI

[18F]AlF-H3RESCA-FAPI

Also written as [F-18]AlF-H3RESCA-FAPI
Radionuclide
F-18 t½ 109.77 min
Modality
Therapy
Production route
Stage
preclinical study
Syntheses indexed
1

What it is

Compound class
FAP-targeted small molecule with H3RESCA chelator (FAPI-based)
Target / mechanism
Fibroblast activation protein (FAP) PMID 40006089
Clinical application
PET imaging of FAP-expressing tumors PMID 40006089
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 synthesiscustom manifoldSPE92.4 ± 2.4%
yes
>95%H3RESCA-FAPI40006089
2025 Pharmaceuticals (Basel)
18F− was loaded onto an activated QMA ion exchange column (Waters GmbH, Eschborn, Germany), which had been previously eluted with 1 mL of saline and air-dried. — the decay-corrected RCY was 92.4 ± 2.4% (n = 6)

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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): 40006089. 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 40006089: 'H3RESCA-FAPI (compound 3) was synthesized (Scheme 1)'. Stage set/updated at stage 23 from PMID 40006089: 'PET imaging was performed in U87MG tumor-bearing mice, with a blocking study to assess tracer specificity.'.