Tracers / [18F]FCPPC

[18F]FCPPC

Also written as [18F]FCPPC
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
Stage
Syntheses indexed
1

What it is

Compound class
CSF1R-targeting radiotracer (CPPC derivative)
Target / mechanism
Colony-stimulating factor 1 receptor (CSF1R), expressed on microglia PMID 39840376
Clinical application
PET imaging of microglia density as a biomarker of neuroinflammation PMID 39840376
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
Synthra RNplus26.8 ± 0.1%
yes
>99%39840376
2024 Am J Nucl Med Mol Imaging
a fully automated radiosynthesis of [18F]FCPPC on a Synthra RNplus research module — [18F]FCPPC was obtained in decay corrected radiochemical yields of 26.8 ± 0.1% (n = 3)

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Quality control Preliminary — inferred from compound class

Ph. Eur. monograph
USP monograph
AppearancepHRCP HPLCRCP TLCHPLC UVRadionuclidic (HPGe)Half-lifeActivityEndotoxins (LAL)SterilityFilter integrity
How this set was arrived at. base set per Ph. Eur. general monograph 0125 (rule); organic-phase radiosynthesis assumed from isotope/compound class, no synthesis data confirming it -> GC residual solvents (preliminary); conventional nucleophilic 18F-fluorination assumed from isotope/compound class, no synthesis data confirming K222 use -> Kryptofix test (preliminary)

Tests listed by reference only. Monograph texts are copyrighted and are not reproduced here. How these are derived

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Notes

Added from reverse module search (stage 6); 1 article(s) with F-18.