Tracers / [64Cu]SarAr-PEG10-Tz

[64Cu]SarAr-PEG10-Tz

Also written as [Cu-64]Cu-SarAr-PEG10-Tz
Radionuclide
Cu-64 t½ 762 min
Modality
Therapy
Production route
Stage
Reported once
Syntheses indexed
1

What it is

Compound class
Sarcophagine-tetrazine bifunctional chelator conjugate (SarAr-PEG10-Tz)
Target / mechanism
Tetrazine-trans-cyclooctene inverse electron-demand Diels-Alder (IEDDA) pretargeting ligation with TCO-bearing huA33 anti-A33 antibody PMID 41605863
Clinical application
Theranostic pair
<a href="/tracers/cu67-sararpeg10tz/">cu67-sararpeg10tz</a>

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
Manual synthesisnone>99%>99%SarAr-PEG10-Tz41605863
2026 Mol Pharm
SarAr-Tz, SarAr-PEG5-Tz, and SarAr-PEG10-Tz (0.7 nmol) were incubated with [64Cu]fCuCl2 (74–370 MBq) in 300 μL ammonium acetate buffer (200 mM, pH 5.5) at room temperature. — >99% radiochemical conversion

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Notes

Added at stage 22: promoted from 'Reported once' (single-article, no diagnostic pair at discovery) because a full-text synthesis with extracted data exists in parsed-therapy.xlsx -- PMID(s): 41605863. 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 41605863: 'SarAr-Tz, SarAr-PEG5-Tz, and SarAr-PEG10-Tz (0.7 nmol) were incubated with [64Cu]fCuCl2'.