Tracers / [11C]FMZ

[11C]FMZ

Also written as [11C]flumazenil; [11C]FMZ; [C-11]flumazenil; [C-11]FMZ; Flumazenil
Radionuclide
C-11 t½ 20.36 min
Modality
PET
Production route
Stage
Syntheses indexed
1

What it is

Compound class
flumazenil derivative (desmethyl flumazenil precursor)
Target / mechanism
Benzodiazepine receptor ligand PMID 36557975
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
iMiDEV
PMB-Alcen
custom manifoldHPLC+SPE22-28% (RCC)>99.00%desmethyl flumazenil
PharmaSynth AS, Tartu, Estonia
36557975
2022 Molecules
iMiDEV™ Automated Microfluidic Radiosynthesizer — The yield of radiochemical conversion for [11C]flumazenil and [11C]deprenyl was 22–28%.

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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)

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 C-11. Compound class inferred from precursor name (not stated outright) -- PMID 36557975: 'desmethyl flumazenil (precursor) and flumazenil (reference standard) were procured from Pharmasynth AS, Tartu, Estonia'.