Tracers / [18F]AlF-OncoFAP-NODAGA

[18F]AlF-OncoFAP-NODAGA

Also written as [18F]AlF-OncoFAP-NODAGA; [F-18]AlF-OncoFAP-NODAGA
Radionuclide
F-18 t½ 109.7 min
Modality
PET
Production route
Cyclotron liquid target
Stage
Research
Syntheses indexed
0

What it is

Compound class
Small molecule chelate
Target / mechanism
FAP PMID 34957527 / DOI 10.1007/s00259-021-05653-0
Clinical application
Theranostic pair
<a href="/tracers/lu177-oncofap-dotaga/">lu177-oncofap-dotaga</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=OncoFAP
EMA (centralised)
Other approvals
Brand names

Clinical use

Typical injected activity
Uptake time

Reported in the literature. Not a dosing recommendation.

Published syntheses

No synthesis has been parsed for this agent yet.

Precursor

Common precursor
NODAGA-OncoFAP conjugate (from OncoFAP-COOH) PMID 36015106 / DOI 10.3390/ph15080958
Suppliers seen in the literature
Typical final purification
HPLC

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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)

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

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Notes

Aluminium fluoride chelation route.