Tracers / [18F]NAV4694

[18F]NAV4694

Also written as [18F]AZD4694; [18F]NAV4694; [F-18]AZD4694; [F-18]NAV4694; AZD4694; F-18 AZD4694; F-18 NAV-4694
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
Stage
Syntheses indexed
2

What it is

Compound class
Target / mechanism
Amyloid-beta (Aβ) PET tracer PMID 39437657
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
39437657
2024 EBioMedicine
SPE13 ± 3 %
yes
99 ± 0.5 %41038002
2025 Appl Radiat Isot
The radiosynthesis was standardised in the FX2N synthesis module — providing the highest radiochemical yield of 13 ± 3 % (decay corrected)

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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); 4 article(s) with F-18.