Tracer library / [18F]6-O-desmethyl-diprenorphine

[18F]6-O-desmethyl-diprenorphine

Also written as [18F]6-O-desmethyl-diprenorphine; [F-18]6-O-desmethyl-diprenorphine
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
—
Stage
—
Syntheses indexed
2

What it is

Compound class
opioid receptor radioligand (diprenorphine derivative)
Target / mechanism
μ-opioid receptors PMID 37685958
Clinical application
PET imaging of brain opioid receptors PMID 37685958
Theranostic pair
—

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
TRACERlab FX FE
GE HealthCare
custom manifoldHPLC44.5 ± 10.6%
decay-corrected
>99%6-O-(2-tosyloxyethyl)-6-O-desmethyl-3-O-trit…6-O-(2-tosyloxyethyl)-6-O-desmethyl-3-O-trityl-diprenorphine (TE-TDDPN)
ABX
37685958
2023 Int J Mol Sci
modified GE Tracerlab FX FE synthesis panel - 44.5 ± 10.6 RCY (decay-corrected)
TRACERlab FX FE
GE HealthCare
—————24692062
2014 J Labelled Comp Radiopharm
GE TRACERlab FXFE radiochemistry module

Precursor

Common precursor
—
Suppliers seen in the literature
—
Cited suppliers in indexed syntheses
ABX
Typical final purification
—

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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.
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