Tracers / [177Lu]Lu-uPAR-02

[177Lu]Lu-uPAR-02

Also written as [Lu-177]Lu-uPAR-02
Radionuclide
Lu-177 t½ 9584.6 min
Modality
Therapy
Production route
Stage
Reported once
Syntheses indexed
1

What it is

Compound class
DOTA-conjugated uPAR-targeting radiopeptide (AE105 backbone) with albumin-binding entity
Target / mechanism
Targets the urokinase-type plasminogen activator receptor (uPAR) PMID 40326657
Clinical application
Cancer (uPAR-expressing tumors) PMID 40326657
Theranostic pair

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 synthesisHPLC>99%uPAR-0240326657
2025 Mol Pharm
The respective amount of peptide (stock solution of 1 mM) and lutetium-177 were added to a 1/5 (v/v) mixture of sodium acetate (0.5 M) and HCl (0.05 M), followed by incubation of the reaction mixture at 95 °C for 10 min

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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): 40326657. 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 40326657: 'uPAR-02 and uPAR-03 were prepared by introducing 3-[2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethoxy]propanoic acid (PEG4)'.