Tracers / [18F]fluspidine

[18F]fluspidine

Also written as [18F]fluspidine
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
Stage
first-in-human / first clinical trial
Syntheses indexed
5

What it is

Compound class
Spirocyclic piperidine (fluspidine, σ1 receptor ligand)
Target / mechanism
σ1 receptor ligand PMID 38399380
Clinical application
PET imaging of σ1 receptors in the brain of patients with major depressive disorder and Huntington's disease (pridopidine occupancy study) PMID 38399380
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
TRACERlab FX FNtosylate precursor (R)-1938399380
2024 Pharmaceuticals (Basel)
automated syntheses were developed using a TRACERlab FX FN synthesis module — the PET tracers [18F]2, (R)-[18F]2 and (S)-[18F]2 were obtained with high radiochemical yields, high radiochemical purity, high molar activity and short reaction times
TRACERlab FX FNtosylate precursor (S)-1938399380
2024 Pharmaceuticals (Basel)
automated syntheses were developed using a TRACERlab FX FN synthesis module — the PET tracers [18F]2, (R)-[18F]2 and (S)-[18F]2 were obtained with high radiochemical yields, high radiochemical purity, high molar activity and short reaction times
tosylate (S)-1728315263
2017 Adv Exp Med Biol
tosylate (R)-1728315263
2017 Adv Exp Med Biol
HPLC+SPE37±8%99.3±0.5%tosylate precursor24291352
2014 Appl Radiat Isot
was implemented on a TRACERlab(TM) FX F-N synthesizer — produced within 59±4 min with an overall radiochemical yield of 37±8%

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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); 3 article(s) with F-18. Stage set/updated at stage 23 from PMID 38399380: 'In the first clinical trial, (S)-[18F]2 was used to visualize σ1 receptors in the brains of patients with major depressive disorder (MDD).'. | Stage 28: added indication(s) neu-huntington from consolidated missing-rubric review.