Tracers / [18F]FBPA

[18F]FBPA

Also written as [18F]FBPA; [F-18]FBPA; FBPA
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
Stage
Syntheses indexed
6

What it is

Compound class
Target / mechanism
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
In-house / custom built27744544
2017 Ann Nucl Med
Radiosynthesis of 18F-FBPA is described in the Supplementary data.
8.5±2.0%98±1%4-borono-L-phenylalanine26159661
2015 Appl Radiat Isot
a modified nucleophilic GE TRACERlab FXFDG — a RCY of 8.5±2.0%
15.5% ± 6.3%
yes
spirocyclic iodonium ylide (SCIDY) precursor42429632
2026 Mol Pharm
using a spirocyclic iodonium ylide (SCIDY) precursor on a commercial module — decay-corrected radiochemical yield of 15.5% ± 6.3%
2.6%
no
BNBA42365564
2026 EJNMMI Radiopharm Chem
0.3%
no
P-0242365564
2026 EJNMMI Radiopharm Chem
3.1%
no
P-0342365564
2026 EJNMMI Radiopharm Chem

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