Tracer library / [18F]PBR102

[18F]PBR102

Also written as [18F]PBR102; [F-18]PBR102
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
—
Stage
Preclinical
Syntheses indexed
2

What it is

Compound class
imidazopyridine (fluoroethoxy-substituted 2-(6-chloro-2-phenyl)imidazo[1,2-a]pyridin-3-yl)-N,N-diethylacetamide)
Target / mechanism
18-kDa translocator protein (TSPO) / peripheral benzodiazepine receptor (PBR) PMID 25231248
Clinical application
Neuroinflammation (preclinical model) PMID 22300959
Theranostic pair
—

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
TRACERlab FX FN
GE HealthCare
——30±2%
not corrected
>99%p-toluenesulfonyl precursors21852142
2012 Appl Radiat Isot
radiosynthesis of [(18)F]PBR111 and [(18)F]PBR102 in the Tracerlab FX(FN) - 30±2% radiochemical yield non-decay-corrected for both tracers
TRACERlab MX
GE HealthCare
——25±2%
not corrected
>99%p-toluenesulfonyl precursors21852142
2012 Appl Radiat Isot
Tracerlab MX(FDG) (25±2% radiochemical yield non-decay-corrected for both tracers) - Tracerlab MX(FDG) (25±2% radiochemical yield non-decay-corrected for both tracers)

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Quality control Preliminary - inferred from compound class

Ph. Eur. monograph
not verified No Ph. Eur. check is recorded for this entry.
USP monograph
not verified No USP check is recorded for this entry.
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.
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