Tracer library / [11C]6-bromopurine
Structure of 6-bromopurine (unlabelled parent compound, from PubChem)
Unlabelled parent compoundPubChem CID 5287830

[11C]6-bromopurine

Also written as [11C]6-bromopurine; [C-11]6-bromopurine
Radionuclide
C-11 t½ 20.36 min
Modality
PET
Production route
—
Stage
Preclinical
Syntheses indexed
1

What it is

Compound class
6-bromo-7-methylpurine derivative (small-molecule purine analogue)
Target / mechanism
Measures multidrug resistance-associated protein 1 (MRP1) transport activity PMID 38683266
Clinical application
Measurement of MRP1 transport activity in tissues, developed toward clinical use in humans PMID 38683266
Theranostic pair
—

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
TRACERlab FX2 C
GE HealthCare
fixed tubingHPLC+SPE20.5 ± 5.2%
decay-corrected
>99%6-bromo-7H-purine
Mihulka, s.r.o., Opava-Jaktar, Czech Republic
38683266
2024 EJNMMI Radiopharm Chem
The automated radiosynthesis was performed in a TRACERlab™ FX2 C synthesis module (GE Healthcare, Uppsala, Sweden). - decay-corrected radiochemical yield of 20.5 ± 5.2%, based on starting [11C]methyl iodide

Precursor

Common precursor
—
Suppliers seen in the literature
—
Cited suppliers in indexed syntheses
Mihulka, s.r.o.
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)

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 38683266: '6-Bromo-7H-purine was synthesised with a purity of 99.2% (HPLC) by Mihulka, s.r.o.'. Stage set/updated at stage 23 from PMID 38683266: 'Advancing 6-bromo-7-[11C]methylpurine to clinical use: improved regioselective radiosynthesis, non-clinical toxicity data and human dosimetry estimates.'. | Stage 30 (2026-09-18): Stage was 'preclinical (non-clinical toxicity study and human dosimetry estimates, prepared to advance to clinical use)'; normalised to 'Preclinical', original wording kept here.
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