Tracer library / [211At]At-211-BC8-B10
[211At]At-211-BC8-B10
Also written as At-211-BC8-B10
- Radionuclide
- At-211 t½ 431 min
- Modality
- Therapy
- Production route
- —
- Stage
- Clinical research
- Syntheses indexed
- 1
What it is
Published syntheses
| Module | Cassette | Purification | Yield % | RCP % | Precursor / supplier | Source |
|---|---|---|---|---|---|---|
| Manual synthesis | custom manifold | SPE | 61±16% not corrected | >97% | BC8-B10 (BC8 conjugated with B10-NCS) | 30335787 2018 PLoS One 211At-labeling of BC8-B10 was conducted by sequential addition of 1.4 mL of 0.5 M ammonium acetate (pH 5.5) and 1.6 mL of 5 mg/mL BC8-B10 solution (8 mg) to an 211At / 0.05 M NaOH solution - the average percent isolated yield of 211At-BC8-B10 was 61±16% |
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Added at stage 21 from therapy-discovered.xlsx (bulk PubMed search by isotope/therapy-type/known-agent, not individually researched yet) -- 2 articles found. Target/mechanism, clinical application, indications, approval and precursor fields still need per-agent research and are intentionally left empty. Compound class inferred from precursor name (not stated outright) -- PMID 30335787: 'BC8-B10 (BC8 conjugated with B10-NCS)'. Stage set/updated at stage 23 from PMID 30335787: 'This study has allowed the initiation of a phase I/II clinical trial using 211At-BC8-B10 (NCT03128034).'. | Stage 28: added indication(s) onc-leukemia from consolidated missing-rubric review. | Stage 30 (2026-09-18): Stage was 'phase I/II clinical trial'; normalised to 'Clinical research', original wording kept here.