Tracers / [131I]iodocarvedilol

[131I]iodocarvedilol

Also written as [I-131]iodocarvedilol
Radionuclide
I-131 t½ 11549 min
Modality
Therapy
Production route
Stage
Syntheses indexed
1

What it is

Compound class
Carvedilol derivative (beta-blocker small molecule)
Target / mechanism
Clinical application
Potential radiopharmaceutical for heart (myocardial) imaging by SPECT PMID 36922888
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 synthesisHPLC92.6 ± 2.77%Carvedilol
Memphis Pharmaceutical Company, Egypt
36922888
2023 BMC Chem
Under oxidative circumstances in the presence of CAT, [131I]iodocarvedilol was frequently produced via direct electrophilic substitution with no carrier added (NCA) 131I. — Carvedilol was labeled with iodine-131 at pH 6 with a labeling yield of 92.6 ± 2.77% by using 100 µg carvedilol, 200 µg chloramin-T (CAT) and 30 min reaction time.

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Notes

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 36922888: 'Carvedilol was purchased from Memphis pharmaceutical company; Egypt and all other chemicals were purchased from Merck and they were analytical reagents.'.