Tracers / [18F]FET-bAG-TOCA

[18F]FET-bAG-TOCA

Also written as [18F]FET-bAG-TOCA; [F-18]FET-bAG-TOCA; FET-bAG-TOCA; fluoroethyl triazole [Tyr3]octreotate
Radionuclide
F-18 t½ 109.7 min
Modality
PET
Production route
Cyclotron liquid target
Stage
Research
Syntheses indexed
3

What it is

Compound class
Peptide (somatostatin analogue)
Target / mechanism
SSTR2 PMID 32252406 / DOI 10.1021/acs.jmedchem.9b02017
Clinical application
Neuroendocrine tumours PMID 27173162; PMID 38331457 / DOI 10.2967/jnumed.123.266383
Theranostic pair
<a href="/tracers/lu177-dotatate/">lu177-dotatate</a>

Regulatory status

FDA
No Drugs@FDA / openFDA drug registry — no approved application found; search: https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=BasicSearch.process&searchTerm=FET-bAG-TOCA
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
FASTlab
GE HealthCare
vendor cassetteHPLC+SPE6.5% ± 2.9%
no
>98%propanyl-βAG-TOCA
ABX
32252406
2020 Cancers (Basel)
the cassette-based GE FASTLab™ platform — The radiosynthesis produced [18F]FET-βAG-TOCA in 6.5% ± 2.9% RCY (n.d.c) with a molar activity >150 GBq/μmol
FASTlab
GE HealthCare
vendor cassetteHPLC+SPE16.7% ± 0.6%
no
propanyl-βAG-TOCA
ABX
32252406
2020 Cancers (Basel)
we investigated new automated methodologies to facilitate CuAAC "click" radiochemistry on the GE FASTLab™ platform — the radiolabelling proceeded efficiently with an isolated radiochemical yield (non-decay corrected) of 16.7% ± 0.6%
42018345
2026 Clin Exp Rheumatol

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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 integrityMolar activity
How this set was arrived at. base set per Ph. Eur. general monograph 0125 (rule); receptor ligand with a saturable target -> molar activity (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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