Tracer library / [11C]evobrutinib

[11C]evobrutinib
Also written as [11C]Evobrutinib; [C-11]Evobrutinib
- Radionuclide
- C-11 t½ 20.36 min
- Modality
- PET
- Production route
- —
- Stage
- Preclinical
- Syntheses indexed
- 3
What it is
Published syntheses
| Module | Cassette | Purification | Yield % | RCP % | Precursor / supplier | Source |
|---|---|---|---|---|---|---|
| TRACERlab FX (model not stated) GE HealthCare | — | HPLC | — | — | — | 37513867 2023 Pharmaceuticals (Basel) a modified GE TracerLabTM synthesis platform - three clinically relevant BTK inhibitors, [11C]ibrutinib, [11C]tolebrutinib, and [11C]evobrutinib, were synthesized at good RCYs |
| TracerMaker Scansys Laboratorieteknik | — | HPLC | 4 not corrected | — | — | 39831838 2025 ChemistryOpen was delivered to a TracerMaker synthesis platform (Scansys Laboratorieteknik, Denmark) - [11C]evobrutinib in RCY of 4 % an Am of 25.3 GBq/μmol |
| — | — | — | 5.5 ± 1.5% | 99% | — | 37691152 2024 J Labelled Comp Radiopharm |
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Get in touchQuality 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.
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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Get in touchNotes
Added from reverse module search (stage 6); 2 article(s) with C-11. Stage set/updated at stage 39 from PMID 37691152: 'Ex vivo autoradiography studies showed high specific binding of [11C]evobrutinib in HT-29 colorectal cancer mouse xenograft tissues (51.1 ± 7.1%).'.