Tracer library / [18F]PM-PBB3

[18F]PM-PBB3

Also written as [18F]APN-1607; [18F]PM-PBB3; [F-18]APN-1607; [F-18]PM-PBB3; APN-1607; PM-PBB3
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
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Stage
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Syntheses indexed
1

What it is

Compound class
Benzothiazole derivative (PBB3 analogue) tau PET tracer
Target / mechanism
Tau pathology PMID 34245396
Clinical application
Clinically used radiotracer for imaging tau pathology PMID 34245396
Theranostic pair
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Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
In-house / custom built
in-house
custom manifoldHPLC16 ± 3.2
decay-corrected
99 ± 0.50PBB3 (7)
Shanghai ChemPartner, Shanghai, China
34245396
2021 EJNMMI Radiopharm Chem
An automated multi-purpose synthesizer developed in-house was used for all the radiosynthetic runs in this study (Supplemental information: Fig. S1, Fukumura et al. 2007). - the radiochemical yield of [18F]PM-PBB3 based on the cyclotron-produced [18F]F− at EOS was 16 ± 3.2 % (n = 11)

Precursor

Common precursor
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Suppliers seen in the literature
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Cited suppliers in indexed syntheses
Shanghai ChemPartner
Typical final purification
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Quality control Preliminary - inferred from compound class

Ph. Eur. monograph
not verified No Ph. Eur. check is recorded for this entry.
USP monograph
not verified No USP check is recorded for this entry.
AppearancepHRCP HPLCRCP TLCHPLC UVRadionuclidic (HPGe)Half-lifeActivityEndotoxins (LAL)SterilityFilter integrity
How this set was arrived at. base set per Ph. Eur. general monograph 0125 (rule); organic-phase radiosynthesis assumed from isotope/compound class, no synthesis data confirming it -> GC residual solvents (preliminary); conventional nucleophilic 18F-fluorination assumed from isotope/compound class, no synthesis data confirming K222 use -> Kryptofix test (preliminary)

Tests listed by reference only. Monograph texts are copyrighted and are not reproduced here. How these are derived

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Notes

Added from reverse module search (stage 6); 4 article(s) with F-18. Compound class inferred from precursor name (not stated outright) -- PMID 34245396: '2-((1E,3E)-4-(6-(methylamino)pyridin-3-yl)buta-1,3-dienyl)benzo[d]thiazol-6-ol (PBB3; 7, Fig. 3)'.
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