Tracer library / [125I]I-Ex-D3

[125I]I-Ex-D3

Radionuclide
I-125 t½ 85666 min
Modality
Therapy
Production route
—
Stage
Reported once
Syntheses indexed
1

What it is

Compound class
Exendin-4 derived peptide (Ex-D3, Glu3Asp substitution with C-terminal Cys, Ex-D3-C40) for site-specific 125I labeling
Target / mechanism
GLP-1 receptor (GLP-1R) agonist binding to pancreatic beta cells PMID 40076236
Clinical application
GLP-1R imaging of pancreatic beta-cells, e.g. for insulinoma-related applications PMID 40076236
Theranostic pair
—

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
Manual synthesis—HPLC43%>99%Ex-D3-C4040076236
2025 Molecules
For radiolabeling peptides, [125I]IPM in acetonitrile was reacted with Ex-D3-C40, Ex-4-C40, or Ex-F1-C40 (100 μg dissolved in PBS) for 30 min at room temperature. - The radiochemical yields for [125I]I-Ex-D3, [125I]I-Ex-4, and [125I]I-Ex-F1 were 43%, 54%, and 59%, respectively

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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): 40076236. 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 40076236: 'Ex-D3-C40, Ex-4-C40, or Ex-F1-C40 were dissolved in PBS (pH 7.4) and added with IPM (1 eq.) to acetonitrile.'.
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