Tracer library / [18F]FMN3PA

[18F]FMN3PA

Also written as [18F]FMN3PA; [F-18]FMN3PA
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
—
Stage
Preclinical
Syntheses indexed
1

What it is

Compound class
LRRK2 kinase inhibitor
Target / mechanism
Leucine-rich repeat kinase 2 (LRRK2) PMID 33248850
Clinical application
Parkinson's disease (LRRK2 G2019S mutation-related) PMID 33248850
Theranostic pair
—

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
TRACERlab FX N
GE HealthCare
—SPE37 ± 1.6%≥96%—33248850
2021 Eur J Med Chem
Radiosyntheses of [18F]FMN3PA (14) and [18F]FMN3PU (15) were performed using K[18F]-F-K222 complex in a TRACERlab FXN module - 37 ± 1.6% (n = 6) ([18F]FMN3PA, 14)

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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); 1 article(s) with F-18. Stage set/updated at stage 39 from PMID 33248850: 'Dynamic scans by PET/CT (Siemens Inveon) were performed in WT mice (n = 3).'.
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