Tracers / [18F]FEAU

[18F]FEAU

Also written as [18F]FEAU; [F-18]FEAU
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
Stage
Syntheses indexed
2

What it is

Compound class
radiolabeled pyrimidine nucleoside analogue
Target / mechanism
Substrate for HSV1-tk/sr39tk enzyme, trapped intracellularly after phosphorylation, enabling reporter gene imaging PMID 18157580
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
TRACERlab FX FNHPLC5±1%
yes
99%18157580
2008 Mol Imaging Biol
a commercial GE TRACERlab FX-FN radiosynthesis module with customized equipment — afforded purified [18F]FEAU β-anomer in 5±1% overall yield (n=3 runs)
ELIXYS FLEX/CHEM
Sofie Biosciences
HPLC28443841
2017 Lab Chip
synthesized using the ELIXYS radiosynthesizer (Sofie Biosciences, Culver City, CA, USA)

Need this precursor?We can point you to suppliers for [18F]FEAU, or handle the enquiry for you.

Get in touch

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

Setting up quality control?We can help you scope the equipment needed to release [18F]FEAU.

Get in touch

Notes

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